Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0002 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0003 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0004 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0005 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0006 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0007 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0008 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| a0009 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | MDAKA others(1243): Show |
chr12 | 98640290 | 98740433 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3744 | 348 | 79 | 57 | 151 | 12 | 47 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0001c0002 | 0/0 | 3744 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0001c0004 | 0/0 | 3744 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0001c0010 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0001c0013 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0002c0003 | 0/0 | 3744 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0003c0005 | 0/0 | 3744 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0004c0006 | 0/0 | 3744 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0005c0007 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0006c0009 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0007c0011 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0008c0012 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
chr12 | 98640290 | 98740433 | ||
| a0009c0008 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | ATGGA others(3739): Show |
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 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0002 | 0/0 | 7200 | 35 | 1 | 3 | 26 | 0 | 5 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0003 | 0/0 | 7200 | 30 | 2 | 0 | 25 | 0 | 3 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0004 | 0/1 | 7200 | 27 | 12 | 7 | 0 | 3 | 4 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0005 | 0/0 | 7201 | 21 | 0 | 0 | 21 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0006 | 0/0 | 7200 | 15 | 0 | 6 | 7 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0007 | 0/0 | 7200 | 2 | 0 | 0 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0008 | 0/0 | 7200 | 7 | 6 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0009 | 0/0 | 7201 | 5 | 5 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0010 | 0/0 | 7201 | 5 | 0 | 0 | 5 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0011 | 0/0 | 7200 | 3 | 0 | 0 | 3 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0012 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0013 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0014 | 0/0 | 7201 | 3 | 2 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0015 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0016 | 0/0 | 7201 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0017 | 0/0 | 7200 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0018 | 0/0 | 7201 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0019 | 0/0 | 7201 | 2 | 0 | 0 | 0 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0020 | 0/0 | 7201 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0021 | 0/0 | 7201 | 2 | 0 | 0 | 1 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0022 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0024 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0026 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0027 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0028 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0030 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0031 | 0/0 | 7201 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0033 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0034 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0035 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0036 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0037 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0038 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0001t0039 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0002t0001 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0002t0023 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0002t0032 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0004t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0001c0010t0001 | 0/0 | 7201 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0001c0013t0006 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0002c0003t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0003c0005t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0004c0006t0001 | 0/0 | 7201 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0005c0007t0029 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0006c0009t0012 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0007c0011t0025 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| a0008c0012t0001 | 0/0 | 7201 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7196): Show |
chr12 | 98640290 | 98740433 |
| a0009c0008t0011 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | AGAGG others(7195): Show |
chr12 | 98640290 | 98740433 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0058 | 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 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0129 | 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 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0160 | 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 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0165 | 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 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0051 | 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 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0065 | 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 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0083 | 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 |
| a0001c0001t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0016g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0016g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0017g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0019g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0019g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0020g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0020g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0021g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0021g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0022g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0024g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0026g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0027g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0028g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0030g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0031g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0033g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0034g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0035g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0036g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0037g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0038g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0039g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0023g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0032g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0004t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0004t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0013t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0002c0003t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0002c0003t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0003c0005t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0003c0005t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0004c0006t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0004c0006t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0005c0007t0029g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0006c0009t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0007c0011t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0008c0012t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0009c0008t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0278 | EUR | GBR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00140 | hp2 | a0001 | c0001 | t0019 | g0206 | EUR | GBR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0174 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0309 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01081 | hp1 | a0001 | c0001 | t0036 | g0290 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01099 | hp1 | a0001 | c0001 | t0020 | g0338 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01109 | hp1 | a0005 | c0007 | t0029 | g0294 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0339 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | 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 | g0158 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01257 | hp2 | a0001 | c0001 | t0017 | g0191 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01258 | hp1 | a0001 | c0001 | t0017 | g0190 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01433 | hp1 | a0001 | c0001 | t0038 | g0302 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0348 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0179 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0178 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0292 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0057 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01891 | hp2 | a0001 | c0001 | t0030 | g0017 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0141 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02004 | hp2 | a0001 | c0001 | t0031 | g0242 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0149 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CDX | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02257 | hp2 | a0001 | c0001 | t0027 | g0201 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02258 | hp2 | a0001 | c0004 | t0007 | g0216 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0153 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02280 | hp2 | a0002 | c0003 | t0007 | g0340 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0212 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0121 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02572 | hp1 | a0003 | c0005 | t0007 | g0210 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0043 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0298 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0008 | 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 | g0203 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0118 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02717 | hp1 | a0006 | c0009 | t0012 | g0202 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02717 | hp2 | a0007 | c0011 | t0025 | g0194 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0306 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02818 | hp1 | a0003 | c0005 | t0007 | g0209 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02886 | hp1 | a0001 | c0001 | t0033 | g0204 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02895 | hp1 | a0001 | c0001 | t0037 | g0289 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0116 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0296 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0295 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0117 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0300 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02970 | hp2 | a0001 | c0002 | t0032 | g0207 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0003 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03139 | hp1 | a0002 | c0003 | t0007 | g0341 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03195 | hp1 | a0001 | c0001 | t0034 | g0198 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03453 | hp2 | a0001 | c0001 | t0028 | g0013 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0299 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0240 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03516 | hp1 | a0001 | c0002 | t0023 | g0297 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03579 | hp2 | a0001 | c0004 | t0007 | g0215 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0119 | 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 | g0305 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0061 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0205 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04204 | hp1 | a0008 | c0012 | t0001 | g0347 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0284 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0123 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0251 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18940 | hp2 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18946 | hp2 | a0004 | c0006 | t0001 | g0343 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18949 | hp2 | a0001 | c0001 | t0021 | g0337 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0138 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0286 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18966 | hp2 | a0001 | c0010 | t0001 | g0001 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18975 | hp2 | a0001 | c0001 | t0011 | g0139 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18982 | hp2 | a0001 | c0001 | t0010 | g0285 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0283 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18993 | hp1 | a0001 | c0013 | t0006 | g0132 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0287 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0016 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19043 | hp2 | a0001 | c0001 | t0039 | g0012 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19054 | hp2 | a0004 | c0006 | t0001 | g0253 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0317 | 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 | g0265 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19065 | hp1 | a0009 | c0008 | t0011 | g0143 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19083 | hp2 | a0001 | c0001 | t0011 | g0126 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19240 | hp1 | a0001 | c0001 | t0015 | g0122 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0291 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | ASW | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0280 | 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 | g0175 | SAS | GIH | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0293 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03471 | hp1 | a0001 | c0001 | t0016 | g0038 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03471 | hp2 | a0001 | c0001 | t0035 | g0176 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | USA | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | USA | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0015 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0193 | REF | REF | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0233 | REF | REF | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| view | 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 | a0005 | 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 | a0009 | 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 | a0008 | 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 | a0006 | 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 |
| view | 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 | a0001c0002 a0002c0003 |
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 |
| view | 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 | a0001c0001t0008 a0001c0001t0022 a0001c0002t0023 |
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 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 others(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 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0038 |
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 | a0001c0001t0036 a0001c0001t0037 |
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 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0038 |
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 | a0005c0007t0029 | 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 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0014 others(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 | a0001c0001t0013 a0005c0007t0029 |
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 | a0001c0001t0009 a0001c0001t0028 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(9): Show |
71 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(68): 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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(161): 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0002t0023 a0001c0002t0032 |
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 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(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 | a0001c0001t0011 a0009c0008t0011 |
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 | a0001c0001t0019 a0001c0001t0020 |
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 |
| view | 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 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0348 others(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 | a0001c0001t0001g0344 | 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 | a0004c0006t0001g0343 | 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 | a0001c0002t0001g0342 a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0018g0015 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): 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 | a0001c0001t0020g0338 a0001c0001t0020g0339 |
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 | 12 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): 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 | a0001c0001t0002g0301 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0018g0015 others(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 | 9 | a0001c0001t0001g0114 a0001c0001t0008g0003 a0001c0001t0008g0295 others(6): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | 106 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0196 others(103): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): 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 | a0001c0001t0001g0350 | 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 | a0001c0001t0002g0310 | 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 | a0001c0001t0002g0310 | 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 | 163 | a0001c0001t0001g0282 a0001c0001t0002g0199 a0001c0001t0002g0211 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0036g0290 | 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0115 | 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 | 83 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(80): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): 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 | a0001c0001t0002g0335 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | 163 | a0001c0001t0001g0282 a0001c0001t0002g0199 a0001c0001t0002g0211 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0004g0195 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0010g0287 | 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 | a0001c0002t0001g0342 | 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 | 83 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(80): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0277 |
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 | a0001c0001t0006g0118 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0007c0011t0025g0194 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | 83 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(80): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): 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 | a0001c0001t0002g0311 | 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 | a0001c0001t0003g0119 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0264 a0001c0001t0001g0265 others(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 | a0001c0001t0037g0289 | 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 | a0001c0001t0004g0120 | 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 | 28 | a0001c0001t0004g0008 a0001c0001t0004g0120 a0001c0001t0004g0168 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+1982delG | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651665 | |||||||
| chr12:98651713 | G | T | 1 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0282 a0001c0001t0010g0281 a0001c0001t0010g0283 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0101 | 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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0012g0208 | 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 52 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(49): 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 | a0001c0001t0010g0286 | 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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0003g0167 | 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 | a0001c0001t0006g0166 | 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 | a0001c0001t0001g0282 a0001c0001t0010g0281 a0001c0001t0010g0283 others(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 | a0001c0002t0032g0207 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0267 a0001c0001t0004g0174 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0282 a0001c0001t0007g0240 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0003g0129 others(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 | 18 | a0001c0001t0003g0119 a0001c0001t0003g0133 a0001c0001t0003g0134 others(15): 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 | 6 | a0001c0001t0003g0007 a0001c0001t0006g0137 a0001c0001t0006g0212 others(3): 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 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0003g0144 others(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 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0004g0181 others(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 | a0001c0001t0003g0165 a0001c0001t0004g0183 a0001c0001t0004g0184 others(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 | a0001c0001t0004g0187 a0001c0001t0012g0208 |
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 | a0001c0001t0004g0188 a0001c0001t0038g0302 |
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 | a0001c0001t0002g0310 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0021g0306 | 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 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0332 others(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 | a0001c0001t0002g0311 | 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 | a0001c0001t0037g0289 | 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 | a0001c0001t0037g0289 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0314 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0002g0312 | 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 | 3 | a0001c0001t0001g0052 a0001c0001t0036g0290 a0001c0001t0037g0289 |
3 | HG01081.hp1 HG02109.hp2 HG02895.hp1 |
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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0004g0168 a0001c0001t0004g0169 a0001c0001t0004g0170 others(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 | a0001c0001t0012g0200 | 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 | 5 | a0001c0001t0001g0052 a0001c0001t0004g0174 a0001c0001t0027g0201 others(2): Show |
5 | HG00280.hp2 HG01081.hp1 HG02109.hp2 others(2): 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 | a0001c0001t0003g0128 | 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 | 2 | a0001c0001t0004g0008 a0001c0001t0004g0195 |
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 | 9 | a0001c0001t0001g0052 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
9 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(6): 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 | a0001c0001t0001g0031 a0001c0001t0005g0035 |
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 | a0001c0001t0005g0068 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0245 | 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 | 18 | a0001c0001t0001g0052 a0001c0001t0001g0282 a0001c0001t0004g0174 others(15): Show |
18 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(15): 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 | a0001c0001t0013g0293 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0086 |
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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0046 |
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 | a0001c0001t0001g0100 | 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 | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0052 others(34): Show |
38 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(35): 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 | a0001c0001t0016g0038 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0025 a0001c0001t0005g0044 a0001c0001t0005g0066 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0097 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0258 a0001c0001t0009g0084 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0252 a0001c0001t0005g0040 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0099 a0001c0001t0001g0102 others(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 | a0001c0001t0005g0065 a0001c0001t0009g0060 |
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 | a0001c0001t0001g0005 a0001c0001t0005g0062 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0078 a0001c0001t0005g0067 |
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 | a0001c0001t0005g0034 | 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 | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0022 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(69): 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0009g0251 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0002 | 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 | a0001c0010t0001g0001 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0020 a0001c0001t0031g0242 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0109 |
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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0045 |
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 | a0001c0001t0001g0002 | 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 | a0001c0001t0005g0006 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0096 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0004c0006t0001g0253 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0278 a0001c0001t0039g0012 |
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 | a0001c0001t0001g0260 a0004c0006t0001g0343 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0261 a0001c0001t0005g0049 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0019 | 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 | 160 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0018 others(157): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0344 |
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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0002t0001g0342 | 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 | a0001c0001t0001g0282 a0001c0001t0010g0281 a0001c0001t0010g0283 others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0012g0203 a0001c0001t0033g0204 a0006c0009t0012g0202 |
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 | a0001c0002t0001g0342 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0007c0011t0025g0194 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0033g0204 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): 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 | 10 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0001t0008g0003 others(7): 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 | a0001c0001t0001g0033 a0001c0001t0001g0101 a0001c0001t0001g0229 others(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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0235 | 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 | 144 | a0001c0001t0001g0282 a0001c0001t0002g0199 a0001c0001t0002g0211 others(141): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): 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 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0311 others(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 | a0001c0001t0003g0131 a0001c0001t0003g0136 a0001c0001t0003g0160 others(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 | 5 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): 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 | a0001c0001t0001g0236 a0001c0001t0002g0199 a0001c0001t0002g0211 others(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 | 8 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(5): 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 | a0001c0001t0001g0237 | 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0080 a0001c0001t0019g0205 a0001c0001t0019g0206 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0003g0124 | 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 | a0001c0001t0001g0018 | 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 | a0001c0002t0001g0342 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0005g0034 | 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 | a0001c0001t0006g0166 | 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 | a0001c0001t0001g0282 a0001c0001t0010g0281 a0001c0001t0010g0283 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0085 |
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 | a0001c0001t0012g0200 | 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 | a0001c0001t0009g0083 a0001c0001t0009g0084 |
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 | a0001c0002t0032g0207 | 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 | 164 | a0001c0001t0001g0282 a0001c0001t0002g0199 a0001c0001t0002g0211 others(161): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0037g0289 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
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 | a0001c0001t0030g0017 | 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 | a0001c0001t0002g0332 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0012g0200 | 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 | a0001c0001t0005g0044 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0037g0289 | 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 | a0001c0001t0001g0045 | 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 | a0007c0011t0025g0194 | 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 | a0007c0011t0025g0194 | 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 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
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 | a0001c0001t0033g0204 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 |
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 | a0001c0001t0010g0285 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0012g0200 | 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 | a0001c0001t0001g0197 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0094 | 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 | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): 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 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0108 others(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 | a0001c0001t0002g0211 a0001c0001t0002g0301 a0001c0001t0002g0311 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0312 a0001c0001t0002g0315 others(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 | a0001c0001t0001g0282 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 5 | a0001c0001t0008g0003 a0001c0001t0008g0298 a0001c0001t0008g0300 others(2): 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 | a0001c0001t0001g0085 a0001c0001t0001g0098 a0001c0001t0005g0081 others(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 | a0001c0002t0001g0342 | 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 | a0001c0001t0001g0029 | 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 | 8 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(5): 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 | a0001c0001t0006g0130 | 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 | a0001c0001t0027g0201 | 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 | a0001c0001t0016g0043 | 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 | 8 | a0001c0001t0004g0008 a0001c0001t0004g0168 a0001c0001t0004g0169 others(5): 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 | a0001c0001t0004g0183 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0019g0206 | 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 | a0001c0001t0010g0283 | 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 | 48 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(45): Show |
49 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.711-1365T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661091 | |||||||
| chr12:98661092 | G | A | 48 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(45): Show |
49 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.711-1364G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661092 | |||||||
| chr12:98661093 | A | G | 48 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(45): Show |
49 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.711-1363A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661093 | |||||||
| chr12:98661109 | A | G | 58 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(55): Show |
59 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(56): 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 | a0001c0001t0012g0208 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0021 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0006g0130 | 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 | a0001c0001t0006g0130 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0006g0130 | 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 | a0001c0001t0036g0290 | 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 | a0001c0001t0012g0208 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0003c0005t0007g0209 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0110 others(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 | a0001c0001t0002g0310 a0001c0001t0012g0200 a0001c0001t0013g0291 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0114 | 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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | 28 | a0001c0001t0004g0008 a0001c0001t0004g0120 a0001c0001t0004g0168 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(26): 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 | a0001c0001t0012g0208 | 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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): 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 | a0001c0001t0006g0130 | 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 | a0001c0001t0006g0130 | 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 | a0001c0001t0006g0130 | 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 | a0001c0001t0003g0125 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0277 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 8 | a0001c0001t0004g0008 a0001c0001t0004g0168 a0001c0001t0004g0169 others(5): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0006g0130 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(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 | a0001c0001t0004g0173 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0005g0074 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0110 | 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 | a0002c0003t0007g0341 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0003g0165 | 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 | a0001c0001t0001g0346 a0001c0001t0001g0348 a0001c0001t0001g0349 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0002t0023g0297 | 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 | a0001c0002t0032g0207 | 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 | a0001c0001t0003g0140 | 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 | a0001c0001t0003g0142 a0001c0001t0003g0145 a0001c0001t0003g0146 others(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 | a0001c0001t0003g0128 a0001c0001t0015g0121 a0001c0001t0015g0122 |
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 | a0001c0001t0003g0163 a0001c0001t0030g0017 a0007c0011t0025g0194 |
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 | a0001c0001t0003g0127 a0001c0001t0004g0184 |
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 | a0001c0001t0003g0144 a0001c0001t0003g0159 |
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 |
4 | a0001c0001t0003g0007 a0001c0001t0003g0125 a0001c0001t0003g0167 others(1): 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 | a0001c0001t0011g0138 | 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 | a0001c0001t0003g0129 a0001c0001t0026g0158 a0009c0008t0011g0143 |
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 | a0001c0001t0003g0124 a0001c0001t0011g0126 a0001c0001t0011g0139 |
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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0311 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0218 |
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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 11 | a0001c0001t0001g0109 a0001c0001t0001g0220 a0001c0001t0001g0230 others(8): 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 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0036 others(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 | a0001c0001t0004g0008 a0001c0001t0004g0168 a0001c0001t0004g0169 others(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 | a0001c0001t0004g0173 a0001c0001t0004g0189 a0001c0001t0004g0192 |
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 | a0001c0001t0003g0151 | 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 | a0001c0001t0004g0182 a0001c0001t0004g0185 a0001c0001t0004g0187 |
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 | a0001c0001t0004g0183 | 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 | a0001c0001t0003g0119 a0001c0001t0003g0133 a0001c0001t0004g0175 others(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 | a0001c0001t0004g0180 a0001c0001t0015g0123 |
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 | a0001c0001t0004g0178 a0001c0001t0004g0179 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0152 |
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 | a0001c0001t0003g0164 | 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 | a0001c0001t0003g0136 | 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 | a0001c0001t0035g0176 | 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 | a0001c0002t0001g0342 | 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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): 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 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0250 a0001c0001t0001g0288 a0001c0001t0009g0083 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0112 others(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 | a0001c0001t0003g0131 a0001c0001t0004g0181 |
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 | a0001c0001t0004g0174 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0229 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0001t0003g0124 a0001c0001t0003g0129 a0001c0001t0011g0139 others(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 | a0001c0001t0011g0139 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | 162 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(159): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): 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 | a0001c0001t0001g0197 a0001c0001t0001g0277 |
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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 68 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(65): Show |
70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | 162 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(159): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1362+215A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98666572 | |||||||
| chr12:98666849 | GTTT | G | 67 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(64): Show |
69 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(66): 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 | 64 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(61): Show |
66 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(63): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0305 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0344 | 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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): 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 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0028 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0313 others(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 | 24 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(21): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0001c0001t0001g0218 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0003g0131 | 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 | a0001c0001t0003g0131 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 4 | a0001c0001t0004g0008 a0001c0001t0004g0168 a0001c0001t0004g0188 others(1): 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0003g0131 | 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 | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(312): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): 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 | a0001c0001t0001g0006 a0001c0001t0005g0006 a0001c0001t0005g0034 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0004g0174 a0001c0001t0013g0291 a0001c0001t0013g0292 others(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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0004g0189 | 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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): 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 | a0001c0001t0004g0180 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0328 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0047 | 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 | a0001c0004t0007g0215 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0001g0025 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): 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 | 155 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(152): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): 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 | a0007c0011t0025g0194 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | a0001c0001t0007g0061 | 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 | a0001c0001t0006g0309 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0003g0159 a0001c0001t0013g0291 a0001c0001t0013g0292 others(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 | a0001c0001t0039g0012 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0286 a0001c0001t0010g0287 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 60 | a0001c0001t0001g0113 a0001c0001t0001g0346 a0001c0001t0002g0199 others(57): 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 | 12 | a0001c0001t0001g0020 a0001c0001t0008g0003 a0001c0001t0008g0295 others(9): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0014g0116 a0001c0001t0014g0117 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 163 | a0001c0001t0001g0115 a0001c0001t0002g0199 a0001c0001t0002g0211 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0002g0310 | 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 | a0001c0001t0005g0039 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0010g0283 | 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 | 68 | a0001c0001t0001g0115 a0001c0001t0002g0329 a0001c0001t0003g0007 others(65): Show |
70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): 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 | a0001c0001t0008g0300 | 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 | a0001c0001t0034g0198 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0005g0039 | 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 | a0001c0002t0001g0342 a0001c0002t0023g0297 a0001c0002t0032g0207 others(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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0003g0164 | 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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0001g0259 | 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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0001g0010 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0106 |
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 | a0001c0001t0020g0339 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 |
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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(307): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): 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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0003c0005t0007g0209 others(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 | 94 | a0001c0001t0001g0020 a0001c0001t0001g0115 a0001c0001t0003g0007 others(91): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1794-360A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677065 | |||||||
| chr12:98677245 | T | C | 70 | a0001c0001t0001g0020 a0001c0001t0001g0115 a0001c0001t0003g0007 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0001g0053 | 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0004g0189 a0001c0001t0004g0192 a0001c0001t0017g0190 others(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 | a0001c0001t0004g0173 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0069 | 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 | 14 | a0001c0001t0004g0008 a0001c0001t0004g0120 a0001c0001t0004g0168 others(11): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0304 | 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 | a0001c0001t0001g0243 | 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 | 70 | a0001c0001t0001g0020 a0001c0001t0001g0115 a0001c0001t0003g0007 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0010g0283 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0305 | 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 | a0001c0001t0031g0242 | 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 | a0001c0001t0009g0060 | 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 | a0001c0001t0003g0167 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(314): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1921-974A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679303 | |||||||
| chr12:98679465 | C | T | 2 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0027g0201 | 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 | a0001c0001t0011g0139 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0007g0061 a0001c0004t0007g0215 |
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 | a0001c0001t0001g0344 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0317 a0001c0001t0002g0333 |
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 | a0005c0007t0029g0294 | 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 | a0001c0001t0006g0156 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0039g0012 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0012g0200 | 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 | a0001c0001t0039g0012 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(313): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0003g0128 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0005g0063 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 |
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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 39 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0073 others(36): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0252 a0001c0001t0003g0150 others(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 | 8 | a0001c0001t0004g0008 a0001c0001t0004g0168 a0001c0001t0004g0169 others(5): 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 | a0001c0001t0002g0310 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0059 a0001c0001t0001g0196 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0059 a0001c0001t0001g0196 others(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 | a0001c0001t0037g0289 | 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 | 350 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(347): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.2047-335A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682808 | |||||||
| chr12:98682811 | T | C | 5 | a0001c0001t0008g0003 a0001c0001t0008g0298 a0001c0001t0008g0299 others(2): 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0003g0151 | 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 | a0001c0001t0003g0128 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | a0001c0001t0008g0295 a0001c0001t0008g0296 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0321 a0001c0001t0002g0327 a0001c0001t0002g0336 others(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 | a0001c0001t0006g0155 | 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 | a0001c0001t0002g0312 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0110 | 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0348 others(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 | a0001c0001t0015g0122 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0003g0124 others(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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0004g0189 a0001c0001t0004g0192 a0001c0001t0017g0190 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0286 a0001c0001t0010g0287 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0004g0180 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0221 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0011 | 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 | 163 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0016g0043 | 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 | a0001c0001t0027g0201 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0006g0141 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0005c0007t0029g0294 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0002g0199 others(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 | a0001c0001t0034g0198 | 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 | a0001c0001t0001g0268 | 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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0001g0048 a0001c0001t0001g0106 |
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 | a0001c0001t0004g0189 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0058 others(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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0002g0313 | 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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): 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 | a0001c0001t0002g0323 a0001c0001t0003g0146 a0001c0001t0012g0203 others(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 | a0001c0001t0001g0058 | 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 | 13 | a0001c0001t0001g0269 a0001c0001t0003g0165 a0001c0001t0004g0177 others(10): 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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): 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 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0037 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0317 a0001c0001t0002g0324 a0001c0001t0002g0335 others(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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0003g0142 a0001c0001t0003g0145 a0001c0001t0003g0146 others(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 | a0001c0001t0008g0295 a0001c0001t0008g0296 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | 8 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0248 | 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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): 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 | 34 | a0001c0001t0001g0115 a0001c0001t0002g0319 a0001c0001t0002g0322 others(31): 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 | a0001c0001t0001g0011 a0001c0001t0002g0199 a0001c0001t0002g0211 others(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 | 68 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(65): Show |
70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): 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 | a0001c0001t0003g0147 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0001g0115 a0001c0001t0010g0285 a0001c0001t0039g0012 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0234 a0001c0001t0001g0239 |
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 | a0001c0001t0010g0285 | 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 | a0001c0001t0001g0115 a0001c0001t0039g0012 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0050 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 12 | a0001c0001t0006g0154 a0001c0001t0008g0003 a0001c0001t0008g0295 others(9): 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 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0271 a0001c0001t0001g0272 others(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 | a0001c0001t0004g0189 a0001c0001t0004g0192 a0001c0001t0017g0190 others(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 | 57 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(54): Show |
59 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(56): 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 | a0001c0001t0003g0131 a0001c0001t0003g0136 a0001c0001t0003g0160 others(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 | a0001c0001t0012g0203 a0001c0001t0033g0204 a0006c0009t0012g0202 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(316): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): 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 | a0001c0001t0001g0350 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0248 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | 70 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2304+4375C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691248 | |||||||
| chr12:98691249 | C | A | 70 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0036g0290 | 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 | 3 | a0001c0001t0008g0003 a0001c0001t0008g0300 a0001c0001t0022g0003 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0003g0127 | 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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0012g0203 a0001c0001t0012g0208 a0001c0001t0033g0204 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0304 a0001c0001t0002g0307 others(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 | a0001c0001t0021g0306 | 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 | a0001c0001t0028g0013 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0004g0175 | 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 | a0001c0002t0001g0342 a0001c0002t0023g0297 a0001c0002t0032g0207 others(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 | a0006c0009t0012g0202 | 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 | a0001c0001t0002g0303 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0012g0200 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0003g0131 a0001c0001t0003g0136 a0001c0001t0003g0160 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0072 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0112 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0053 a0001c0001t0007g0061 |
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 | a0001c0001t0016g0038 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 94 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(91): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.2305-5092A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694316 | |||||||
| chr12:98694445 | A | T | 70 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0030 a0001c0001t0002g0321 a0001c0001t0002g0327 others(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 | a0001c0001t0003g0165 | 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 | a0001c0001t0004g0173 | 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 | a0001c0001t0003g0150 a0001c0001t0003g0152 |
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 | a0001c0001t0003g0213 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0039g0012 a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0086 others(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 | a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0001c0001t0001g0260 a0001c0001t0002g0211 a0001c0001t0002g0326 others(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 | a0001c0001t0001g0014 | 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 | a0001c0002t0001g0342 a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0003g0165 | 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 | a0001c0001t0001g0248 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0255 a0001c0001t0001g0278 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0020 | 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 | a0002c0003t0007g0340 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0009g0060 a0001c0001t0009g0251 |
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 | a0001c0001t0001g0266 a0001c0001t0005g0049 a0001c0001t0005g0066 others(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 | 13 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0177 others(10): Show |
13 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(10): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0346 | 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 | a0001c0002t0023g0297 a0001c0002t0032g0207 |
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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0124 a0001c0001t0003g0125 others(5): 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0004c0006t0001g0253 a0004c0006t0001g0343 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0003g0127 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0011 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0006g0154 a0001c0001t0006g0157 |
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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0005c0007t0029g0294 | 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 | a0001c0001t0018g0015 a0001c0001t0018g0016 |
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 | 6 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): 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 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0311 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0003c0005t0007g0209 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0036g0290 | 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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): 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 | a0001c0002t0023g0297 a0001c0002t0032g0207 |
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 | a0001c0001t0038g0302 | 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 | 37 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(34): 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 | a0001c0001t0002g0301 a0001c0001t0002g0314 a0001c0001t0002g0315 others(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 | a0001c0001t0004g0174 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0278 |
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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(314): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 37 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(34): 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): 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 | a0001c0001t0012g0203 a0001c0001t0033g0204 a0006c0009t0012g0202 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0024g0149 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 50 | a0001c0001t0001g0115 a0001c0001t0001g0259 a0001c0001t0001g0280 others(47): 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0237 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0003g0142 a0001c0001t0003g0145 a0001c0001t0003g0146 others(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 | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(313): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0003c0005t0007g0209 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0002g0301 a0001c0001t0002g0314 a0001c0001t0002g0315 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0089 others(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 | 70 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(67): Show |
72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0225 | 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 | a0001c0002t0001g0342 a0001c0002t0023g0297 a0001c0002t0032g0207 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | a0005c0007t0029g0294 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0020g0339 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | 36 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(33): 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 | a0001c0001t0005g0039 | 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 | a0001c0001t0003g0164 | 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 | a0001c0001t0002g0329 | 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 | a0001c0001t0002g0321 a0001c0001t0002g0327 a0001c0001t0002g0336 others(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 | a0001c0001t0027g0201 | 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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0015g0121 a0001c0001t0015g0122 |
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 | a0001c0002t0023g0297 a0001c0002t0032g0207 |
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 | a0001c0001t0007g0061 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 |
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 | a0001c0001t0014g0284 | 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 | 164 | a0001c0001t0001g0115 a0001c0001t0002g0199 a0001c0001t0002g0211 others(161): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2722-953G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707632 | |||||||
| chr12:98707663 | T | C | 94 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(91): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(93): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
141 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(138): 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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0109 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0038g0302 | 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 | a0001c0001t0002g0301 a0001c0001t0002g0310 a0001c0001t0002g0324 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0311 a0001c0001t0002g0314 others(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 | a0001c0001t0002g0312 a0001c0001t0002g0321 a0001c0001t0006g0156 others(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 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0336 others(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 | a0001c0001t0002g0305 | 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 | a0001c0001t0002g0211 | 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 | a0001c0001t0002g0307 a0001c0001t0002g0308 |
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 | a0001c0001t0002g0304 a0001c0001t0007g0240 |
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 | a0001c0001t0002g0303 | 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 | a0001c0001t0002g0313 | 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 | a0001c0001t0006g0155 | 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 | a0001c0001t0002g0330 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0030g0017 |
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 | a0005c0007t0029g0294 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0003g0128 a0001c0001t0003g0133 a0001c0001t0003g0134 others(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 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0260 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0034g0198 | 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 | a0001c0001t0004g0195 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0002t0023g0297 | 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 | a0001c0001t0036g0290 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0002g0211 a0001c0001t0002g0303 a0001c0001t0002g0304 others(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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 36 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(33): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0046 others(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 | 63 | a0001c0001t0003g0007 a0001c0001t0003g0124 a0001c0001t0003g0125 others(60): Show |
65 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(62): 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 | a0001c0001t0001g0273 a0001c0001t0003g0119 a0001c0001t0003g0131 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0303 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | 156 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(153): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0013g0293 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0005g0006 others(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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
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 | a0001c0001t0003g0161 | 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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): 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 | a0001c0001t0004g0186 | 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 | a0001c0001t0004g0180 | 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 | a0001c0001t0002g0211 | 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 | a0001c0001t0001g0350 a0001c0001t0002g0199 a0001c0001t0002g0211 others(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 | 163 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2958+154C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712589 | |||||||
| chr12:98712664 | A | G | 163 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(160): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0005g0107 | 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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0006g0214 | 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 | a0001c0001t0002g0199 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 |
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 | 7 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0184 |
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 | a0001c0001t0001g0076 | 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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): 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 | a0001c0001t0001g0031 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0248 | 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 | 13 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0177 others(10): Show |
13 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(10): 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 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0033 others(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 | a0001c0001t0014g0116 a0001c0001t0014g0117 |
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 | 164 | a0001c0001t0001g0115 a0001c0001t0002g0199 a0001c0001t0002g0211 others(161): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0272 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0230 a0001c0001t0003g0160 a0001c0001t0003g0167 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0225 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0218 a0001c0001t0001g0226 others(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 |
4 | a0001c0001t0002g0305 a0001c0001t0004g0183 a0001c0001t0008g0295 others(1): Show |
4 | HG00738.hp1 HG02896.hp1 HG02897.hp1 others(1): 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 | a0001c0001t0015g0123 | 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 | a0001c0001t0003g0125 | 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 | a0001c0001t0003g0148 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0033 others(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 | 11 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0087 others(8): 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 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0012g0203 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0093 others(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 | 26 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): 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 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0005g0006 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0249 a0001c0001t0024g0149 others(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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
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 | a0001c0001t0002g0321 a0001c0001t0002g0334 a0001c0001t0006g0212 |
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 | a0001c0001t0002g0321 a0001c0001t0002g0334 a0001c0001t0006g0212 |
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 | a0001c0001t0002g0318 | 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 | a0001c0001t0002g0312 a0001c0001t0006g0118 a0001c0001t0006g0130 |
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 | a0001c0001t0002g0327 | 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 | a0001c0001t0002g0329 a0001c0001t0002g0333 |
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 | a0001c0001t0002g0311 a0001c0001t0002g0320 a0001c0001t0002g0332 others(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 | a0001c0001t0002g0301 a0001c0001t0002g0314 a0001c0001t0002g0316 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0315 a0001c0001t0002g0319 others(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 | a0001c0001t0006g0141 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0014g0284 | 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 | a0001c0001t0001g0350 | 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 | a0001c0002t0001g0342 a0001c0002t0023g0297 a0001c0002t0032g0207 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 164 | a0001c0001t0001g0115 a0001c0001t0002g0199 a0001c0001t0002g0211 others(161): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.3084+1117T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716669 | |||||||
| chr12:98716915 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): 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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0012g0208 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0085 a0001c0001t0001g0113 |
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 | a0001c0001t0001g0101 a0001c0001t0013g0291 a0001c0001t0013g0292 others(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 | a0001c0001t0036g0290 a0001c0001t0037g0289 a0001c0004t0007g0215 others(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 | a0001c0001t0013g0291 | 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 | a0001c0001t0024g0149 | 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 | a0001c0001t0013g0291 | 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 | a0001c0001t0013g0291 | 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 | a0001c0001t0036g0290 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0024g0149 | 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 | a0001c0001t0036g0290 | 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 | a0001c0004t0007g0215 a0001c0004t0007g0216 |
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 | a0001c0001t0004g0120 | 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 | a0001c0001t0002g0301 a0001c0001t0002g0314 a0001c0001t0002g0315 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): 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 | 134 | a0001c0001t0001g0115 a0001c0001t0002g0199 a0001c0001t0002g0211 others(131): Show |
136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0056 |
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 | a0001c0001t0004g0171 | 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 | a0001c0001t0006g0162 | 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 | a0001c0001t0003g0167 | 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 | a0001c0001t0001g0245 a0001c0001t0004g0173 a0001c0001t0008g0296 others(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 | a0001c0001t0001g0258 | 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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0024g0149 | 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 | a0001c0002t0023g0297 a0001c0002t0032g0207 |
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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
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 | a0001c0001t0004g0169 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0001g0266 | 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 | 15 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0177 others(12): Show |
15 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(12): 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 | a0001c0001t0001g0266 | 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 | 9 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(6): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0027g0201 | 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 | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(311): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): 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 | a0001c0001t0003g0165 | 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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 190 | a0001c0001t0001g0059 a0001c0001t0001g0243 a0001c0001t0001g0244 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | 69 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(66): Show |
71 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(68): 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0006g0118 a0001c0001t0006g0141 a0001c0001t0006g0153 others(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 | a0001c0001t0005g0042 | 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 | a0001c0001t0001g0050 a0001c0001t0009g0057 a0001c0001t0009g0060 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0231 | 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 | a0002c0003t0007g0340 a0002c0003t0007g0341 |
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 | a0001c0001t0001g0228 | 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 | 21 | a0001c0001t0001g0092 a0001c0001t0008g0003 a0001c0001t0008g0298 others(18): 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 | a0001c0001t0001g0096 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 |
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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 67 | a0001c0001t0001g0077 a0001c0001t0001g0113 a0001c0001t0001g0115 others(64): Show |
69 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(66): 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 | a0001c0001t0001g0056 a0001c0001t0002g0199 a0001c0001t0002g0211 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | a0001c0001t0005g0065 a0001c0001t0005g0068 |
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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0003g0134 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0004g0189 a0001c0001t0004g0192 a0001c0001t0017g0190 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): 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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): 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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): 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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): 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 | 92 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(89): 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 | 15 | a0001c0001t0004g0008 a0001c0001t0004g0120 a0001c0001t0004g0168 others(12): 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 | a0001c0001t0009g0251 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0003g0148 | 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 | 11 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(8): 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0286 |
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 | a0001c0001t0027g0201 | 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 | a0001c0004t0007g0216 | 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 | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(311): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): 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 | a0001c0004t0007g0215 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0002t0001g0342 | 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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 66 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(63): Show |
68 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(65): 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 | a0001c0001t0003g0148 | 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 | a0001c0004t0007g0215 | 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 | a0001c0004t0007g0216 | 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 | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(302): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): 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 | a0007c0011t0025g0194 | 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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.3600+454G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727770 | |||||||
| chr12:98727785 | A | C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(33): 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 |
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 | a0001c0001t0019g0205 a0001c0001t0019g0206 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | 21 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(18): 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 | a0001c0001t0002g0326 a0001c0001t0007g0240 |
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 | 16 | a0001c0001t0001g0054 a0001c0001t0001g0277 a0001c0001t0001g0278 others(13): 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 | a0001c0001t0001g0260 a0001c0001t0013g0291 a0001c0001t0013g0292 others(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 | a0001c0001t0010g0281 a0001c0001t0010g0283 a0001c0001t0010g0285 others(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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.3600+654T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727970 | |||||||
| chr12:98727974 | T | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0082 others(24): 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 | 69 | a0001c0001t0003g0007 a0001c0001t0003g0119 a0001c0001t0003g0124 others(66): Show |
71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.3600+1230G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728546 | |||||||
| chr12:98728557 | TA | T | 160 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(157): Show |
163 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(160): 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 | a0001c0001t0012g0200 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | 13 | a0001c0001t0008g0003 a0001c0001t0008g0295 a0001c0001t0008g0296 others(10): 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 | a0001c0001t0005g0074 | 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 | a0001c0001t0005g0039 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0102 others(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 | a0001c0002t0001g0342 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0093 | 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 | a0003c0005t0007g0209 a0003c0005t0007g0210 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | a0001c0001t0004g0172 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0316 a0001c0001t0002g0317 others(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 | a0001c0001t0001g0349 | 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 | 66 | a0001c0001t0001g0115 a0001c0001t0003g0007 a0001c0001t0003g0119 others(63): Show |
68 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(65): 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0027g0201 | 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 | a0001c0001t0010g0283 | 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 | a0001c0001t0019g0205 a0001c0001t0019g0206 a0001c0001t0020g0338 others(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 | a0001c0001t0024g0149 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0301 others(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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0003g0165 | 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 | a0001c0001t0013g0291 a0001c0001t0013g0292 a0001c0001t0013g0293 others(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 | a0001c0001t0007g0240 | 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 | a0001c0001t0036g0290 a0001c0001t0037g0289 |
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 | a0001c0001t0012g0200 a0001c0001t0013g0291 a0001c0001t0013g0292 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0015g0121 a0001c0001t0015g0122 a0001c0001t0015g0123 others(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 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0344 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3601-94G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98732326 |