Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 200558 |
| ensemblid | ENSG00000169621.11 |
| hgncid | 28724 |
| symbol | APLF |
| name | aprataxin and PNKP like factor |
| refseq_nuc | NM_173545.3 |
| refseq_prot | NP_775816.1 |
| ensembl_nuc | ENST00000303795.9 |
| ensembl_prot | ENSP00000307004.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 68467585 |
| end | 68580162 |
| strand | + |
| ver | v1.2 |
| region | chr2:68467585-68580162 |
| region5000 | chr2:68462585-68585162 |
| regionname0 | APLF_chr2_68467585_68580162 |
| regionname5000 | APLF_chr2_68462585_68585162 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 511 | 84 | 25 | 18 | 21 | 3 | 15 | 18 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0002 | 0/0 | 511 | 39 | 33 | 6 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0003 | 0/0 | 511 | 21 | 14 | 5 | 0 | 1 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0004 | 0/0 | 511 | 13 | 0 | 2 | 7 | 2 | 2 | 6 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0005 | 0/0 | 510 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(505): Show |
chr2 | 68462585 | 68585162 |
| a0006 | 0/0 | 511 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0007 | 0/0 | 511 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0008 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0009 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0010 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0011 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| a0012 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | MSGGF others(506): Show |
chr2 | 68462585 | 68585162 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1533 | 83 | 25 | 18 | 20 | 3 | 15 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0001c0009 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0002c0002 | 0/0 | 1533 | 38 | 32 | 6 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0002c0011 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0003c0003 | 0/0 | 1533 | 21 | 14 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0004c0004 | 0/0 | 1533 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0005c0005 | 0/0 | 1530 | 5 | 0 | 3 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1525): Show |
chr2 | 68462585 | 68585162 | ||
| a0006c0007 | 0/0 | 1533 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0006c0013 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0007c0006 | 0/0 | 1533 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0008c0010 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0009c0008 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0010c0014 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0011c0012 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 | ||
| a0012c0015 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | ATGTC others(1528): Show |
chr2 | 68462585 | 68585162 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3823 | 80 | 24 | 18 | 18 | 3 | 15 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0001c0001t0011 | 0/0 | 3823 | 2 | 0 | 0 | 2 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0001c0001t0015 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0001c0009t0001 | 0/0 | 3823 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0002 | 0/0 | 3824 | 20 | 18 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0006 | 0/0 | 3816 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0007 | 0/0 | 3824 | 5 | 2 | 3 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0008 | 0/0 | 3824 | 3 | 2 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0009 | 0/0 | 3824 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0010 | 0/0 | 3824 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0002c0002t0012 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0002c0011t0002 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0003c0003t0004 | 0/0 | 3824 | 12 | 5 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0003c0003t0005 | 0/0 | 3824 | 9 | 9 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0004c0004t0003 | 0/0 | 3824 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0005c0005t0001 | 0/0 | 3820 | 4 | 0 | 2 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3815): Show |
chr2 | 68462585 | 68585162 |
| a0005c0005t0014 | 0/0 | 3820 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3815): Show |
chr2 | 68462585 | 68585162 |
| a0006c0007t0006 | 0/0 | 3816 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0006c0007t0017 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0006c0013t0016 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0007c0006t0001 | 0/0 | 3823 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0008c0010t0001 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3818): Show |
chr2 | 68462585 | 68585162 |
| a0009c0008t0006 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3811): Show |
chr2 | 68462585 | 68585162 |
| a0010c0014t0009 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0011c0012t0007 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| a0012c0015t0013 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | GAGAG others(3819): Show |
chr2 | 68462585 | 68585162 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0001c0009t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0008g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0002t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0002c0011t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0003c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0004c0004t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0005c0005t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0005c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0005c0005t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0005c0005t0014g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0006c0007t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0006c0007t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0006c0007t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0006c0013t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0007c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0007c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0007c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0007c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0008c0010t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0009c0008t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0010c0014t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0011c0012t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| a0012c0015t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00639 | hp1 | a0003 | c0003 | t0004 | g0118 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00639 | hp2 | a0005 | c0005 | t0001 | g0153 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00673 | hp2 | a0001 | c0009 | t0001 | g0154 | EAS | CHS | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00738 | hp1 | a0003 | c0003 | t0004 | g0125 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01109 | hp1 | a0002 | c0002 | t0007 | g0030 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01109 | hp2 | a0005 | c0005 | t0014 | g0141 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01167 | hp1 | a0002 | c0002 | t0007 | g0001 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01167 | hp2 | a0002 | c0002 | t0008 | g0025 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01169 | hp1 | a0002 | c0002 | t0007 | g0001 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01192 | hp1 | a0003 | c0003 | t0004 | g0123 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01192 | hp2 | a0005 | c0005 | t0001 | g0148 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01261 | hp2 | a0003 | c0003 | t0004 | g0113 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01884 | hp1 | a0007 | c0006 | t0001 | g0140 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01943 | hp1 | a0003 | c0003 | t0004 | g0114 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0024 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02055 | hp2 | a0007 | c0006 | t0001 | g0135 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02129 | hp1 | a0004 | c0004 | t0003 | g0011 | EAS | KHV | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02257 | hp1 | a0003 | c0003 | t0005 | g0129 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02280 | hp1 | a0002 | c0002 | t0006 | g0161 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02293 | hp1 | a0004 | c0004 | t0003 | g0010 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02300 | hp2 | a0004 | c0004 | t0003 | g0015 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02451 | hp2 | a0002 | c0002 | t0010 | g0168 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02572 | hp2 | a0003 | c0003 | t0005 | g0127 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02615 | hp1 | a0007 | c0006 | t0001 | g0139 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02615 | hp2 | a0003 | c0003 | t0004 | g0122 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02622 | hp1 | a0002 | c0002 | t0006 | g0160 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02622 | hp2 | a0010 | c0014 | t0009 | g0032 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02717 | hp2 | a0003 | c0003 | t0005 | g0131 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02738 | hp1 | a0004 | c0004 | t0003 | g0016 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02738 | hp2 | a0005 | c0005 | t0001 | g0152 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02895 | hp1 | a0002 | c0002 | t0009 | g0003 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02897 | hp2 | a0002 | c0002 | t0009 | g0003 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02965 | hp1 | a0003 | c0003 | t0005 | g0133 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02970 | hp1 | a0003 | c0003 | t0004 | g0121 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03041 | hp2 | a0002 | c0002 | t0010 | g0166 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03098 | hp1 | a0006 | c0007 | t0006 | g0002 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0089 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03130 | hp1 | a0003 | c0003 | t0005 | g0104 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03139 | hp2 | a0003 | c0003 | t0005 | g0128 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03195 | hp1 | a0006 | c0007 | t0017 | g0023 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03209 | hp1 | a0002 | c0002 | t0007 | g0031 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03225 | hp1 | a0003 | c0003 | t0005 | g0130 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03225 | hp2 | a0002 | c0002 | t0012 | g0022 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03453 | hp2 | a0003 | c0003 | t0004 | g0150 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03486 | hp1 | a0006 | c0013 | t0016 | g0165 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03486 | hp2 | a0006 | c0007 | t0006 | g0002 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03516 | hp2 | a0002 | c0002 | t0010 | g0167 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03540 | hp1 | a0011 | c0012 | t0007 | g0028 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0120 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03579 | hp1 | a0007 | c0006 | t0001 | g0138 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0124 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03942 | hp2 | a0004 | c0004 | t0003 | g0013 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG04228 | hp2 | a0005 | c0005 | t0001 | g0143 | SAS | STU | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18522 | hp2 | a0012 | c0015 | t0013 | g0164 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18906 | hp1 | a0003 | c0003 | t0005 | g0132 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18943 | hp2 | a0004 | c0004 | t0003 | g0021 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18966 | hp1 | a0004 | c0004 | t0003 | g0017 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0082 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18978 | hp1 | a0004 | c0004 | t0003 | g0019 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA18984 | hp2 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19005 | hp1 | a0004 | c0004 | t0003 | g0018 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19058 | hp1 | a0004 | c0004 | t0003 | g0014 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19079 | hp1 | a0004 | c0004 | t0003 | g0012 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19240 | hp1 | a0006 | c0007 | t0006 | g0033 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | ASW | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20129 | hp2 | a0002 | c0002 | t0008 | g0026 | AFR | ASW | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20752 | hp1 | a0004 | c0004 | t0003 | g0009 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20805 | hp1 | a0003 | c0003 | t0004 | g0103 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20805 | hp2 | a0004 | c0004 | t0003 | g0020 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02109 | hp1 | a0002 | c0002 | t0006 | g0162 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02109 | hp2 | a0008 | c0010 | t0001 | g0110 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02486 | hp1 | a0009 | c0008 | t0006 | g0027 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03471 | hp1 | a0003 | c0003 | t0005 | g0126 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0029 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| HG06807 | hp2 | a0002 | c0011 | t0002 | g0049 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20300 | hp1 | a0002 | c0002 | t0006 | g0163 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| NA21309 | hp2 | a0003 | c0003 | t0004 | g0119 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0077 | REF | REF | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0151 | REF | REF | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:68502860 | A | G | 6 | a0002 a0004 a0006 others(3): Show |
60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
missense_variant | MODERATE | c.298A>G | p.Ile100Val | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/10 | 445/3823 | 298/1536 | 100/511 | chr2 | 68502860 | |||
| chr2:68513576 | A | G | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.518A>G | p.Asn173Ser | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/10 | 665/3823 | 518/1536 | 173/511 | chr2 | 68513576 | |||
| chr2:68526108 | T | A | 7 | a0002 a0003 a0004 others(4): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
missense_variant | MODERATE | c.670T>A | p.Ser224Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/10 | 817/3823 | 670/1536 | 224/511 | chr2 | 68526108 | |||
| chr2:68538002 | AAAG | A | 1 | a0005 | 5 | HG00639.hp2 HG01109.hp2 HG01192.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.938_940delGAA | p.Arg313del | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1085/3823 | 938/1536 | 313/511 | INFO_REALIGN_3_PRIME | chr2 | 68538002 | ||
| chr2:68538073 | C | T | 2 | a0003 a0006 |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
missense_variant | MODERATE | c.1006C>T | p.Leu336Phe | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1153/3823 | 1006/1536 | 336/511 | chr2 | 68538073 | |||
| chr2:68545278 | C | T | 1 | a0011 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1252C>T | p.Arg418Trp | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1399/3823 | 1252/1536 | 418/511 | chr2 | 68545278 | |||
| chr2:68545302 | T | C | 1 | a0007 | 4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.1276T>C | p.Ser426Pro | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1423/3823 | 1276/1536 | 426/511 | chr2 | 68545302 | |||
| chr2:68545305 | T | C | 1 | a0012 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1279T>C | p.Cys427Arg | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1426/3823 | 1279/1536 | 427/511 | chr2 | 68545305 | |||
| chr2:68567351 | C | A | 1 | a0004 | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
missense_variant | MODERATE | c.1297C>A | p.Gln433Lys | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/10 | 1444/3823 | 1297/1536 | 433/511 | chr2 | 68567351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:68502799 | A | G | 2 | a0004c0004 a0012c0015 |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
synonymous_variant | LOW | c.237A>G | p.Leu79Leu | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/10 | 384/3823 | 237/1536 | 79/511 | chr2 | 68502799 | |||
| chr2:68538153 | T | C | 1 | a0006c0013 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1086T>C | p.Thr362Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1233/3823 | 1086/1536 | 362/511 | chr2 | 68538153 | |||
| chr2:68567350 | C | T | 1 | a0002c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1296C>T | p.Pro432Pro | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/10 | 1443/3823 | 1296/1536 | 432/511 | chr2 | 68567350 | |||
| chr2:68577923 | A | C | 1 | a0001c0009 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1437A>C | p.Thr479Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1584/3823 | 1437/1536 | 479/511 | chr2 | 68577923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:68467605 | G | C | 1 | a0002c0002t0012 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/10 | 127 | chr2 | 68467605 | ||||||
| chr2:68467715 | C | T | 1 | a0001c0001t0011 | 2 | NA18971.hp1 NA18984.hp2 |
5_prime_UTR_variant | MODIFIER | c.-17C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/10 | 17 | chr2 | 68467715 | ||||||
| chr2:68578612 | G | A | 1 | a0012c0015t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 590 | chr2 | 68578612 | ||||||
| chr2:68578785 | C | T | 10 | a0002c0002t0006 a0002c0002t0010 a0002c0002t0012 others(7): Show |
36 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*763C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 763 | chr2 | 68578785 | ||||||
| chr2:68578970 | A | G | 2 | a0002c0002t0002 a0002c0011t0002 |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 948 | chr2 | 68578970 | ||||||
| chr2:68578987 | G | A | 2 | a0002c0002t0002 a0002c0011t0002 |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 965 | chr2 | 68578987 | ||||||
| chr2:68579085 | C | T | 1 | a0006c0007t0017 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1063 | chr2 | 68579085 | ||||||
| chr2:68579304 | T | A | 1 | a0005c0005t0014 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1282 | chr2 | 68579304 | ||||||
| chr2:68579411 | A | G | 1 | a0012c0015t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1389 | chr2 | 68579411 | ||||||
| chr2:68579453 | G | A | 11 | a0002c0002t0006 a0002c0002t0008 a0002c0002t0010 others(8): Show |
39 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1431G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1431 | chr2 | 68579453 | ||||||
| chr2:68579540 | A | AT | 18 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0007 others(15): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1518_*1519insT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1519 | chr2 | 68579540 | ||||||
| chr2:68579543 | C | G | 2 | a0002c0002t0007 a0011c0012t0007 |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1521C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1521 | chr2 | 68579543 | ||||||
| chr2:68579551 | TATCAACT others(1): Show |
T | 6 | a0002c0002t0006 a0002c0002t0012 a0006c0007t0006 others(3): Show |
11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1530_*1537delATCA others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1530 | chr2 | 68579551 | ||||||
| chr2:68579558 | TG | T | 12 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0008 others(9): Show |
71 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1539delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1539 | INFO_REALIGN_3_PRIME | chr2 | 68579558 | |||||
| chr2:68579561 | G | A | 1 | a0001c0001t0015 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1539 | chr2 | 68579561 | ||||||
| chr2:68579734 | C | T | 1 | a0002c0002t0010 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1712C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1712 | chr2 | 68579734 | ||||||
| chr2:68579813 | G | A | 1 | a0004c0004t0003 | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1791G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1791 | chr2 | 68579813 | ||||||
| chr2:68579951 | T | C | 5 | a0002c0002t0006 a0002c0002t0012 a0006c0007t0006 others(2): Show |
10 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1929T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1929 | chr2 | 68579951 | ||||||
| chr2:68580092 | C | T | 1 | a0003c0003t0004 | 12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2070C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 2070 | chr2 | 68580092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:68467851 | G | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.96+24G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467851 | |||||||
| chr2:68467897 | C | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+70C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467897 | |||||||
| chr2:68467908 | C | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+81C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467908 | |||||||
| chr2:68467927 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+100G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467927 | |||||||
| chr2:68467954 | T | A | 2 | a0002c0002t0012g0022 a0012c0015t0013g0164 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.96+127T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467954 | |||||||
| chr2:68467976 | A | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+149A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467976 | |||||||
| chr2:68468070 | G | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+243G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468070 | |||||||
| chr2:68468159 | T | C | 58 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(55): Show |
61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+332T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468159 | |||||||
| chr2:68468321 | C | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+494C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468321 | |||||||
| chr2:68468387 | A | G | 33 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(30): Show |
36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.96+560A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468387 | |||||||
| chr2:68468438 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+611A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468438 | |||||||
| chr2:68468480 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.96+653G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468480 | |||||||
| chr2:68468485 | C | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+658C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468485 | |||||||
| chr2:68468512 | T | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+685T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468512 | |||||||
| chr2:68468825 | C | T | 24 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(21): Show |
26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.96+998C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468825 | |||||||
| chr2:68468969 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+1142A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468969 | |||||||
| chr2:68468989 | G | GGT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
12 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1193_96+1194dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | G | GGTGT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.96+1191_96+1194dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | G | GGTGTGT | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
7 | HG01943.hp2 HG02109.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+1189_96+1194dup others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | G | GGTGTGTG others(1): Show |
5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0002c0002t0006g0160 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1187_96+1194dup others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | G | GTGT | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG03579.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.96+1162_96+1163ins others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468989 | |||||||
| chr2:68468989 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.96+1162G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468989 | |||||||
| chr2:68468989 | GGT | G | 7 | a0001c0001t0001g0156 a0002c0002t0009g0003 a0002c0002t0010g0166 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1193_96+1194del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | GGTGT | G | 7 | a0002c0002t0012g0022 a0004c0004t0003g0009 a0004c0004t0003g0010 others(4): Show |
7 | HG02129.hp1 HG02293.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+1191_96+1194del others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468989 | GGTGTGT | G | 9 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(6): Show |
9 | HG02300.hp2 HG02738.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1189_96+1194del others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | ||||||
| chr2:68468991 | T | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG02280.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1164T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468991 | |||||||
| chr2:68469014 | G | GTGTGTGT | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1207_96+1213dup others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | ||||||
| chr2:68469014 | G | GTGTGTGT others(4): Show |
1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+1194_96+1195ins others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | ||||||
| chr2:68469014 | GTGTGTGT | G | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(5): Show |
8 | HG01243.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1207_96+1213del others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | ||||||
| chr2:68469016 | GTGTGT | G | 10 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(7): Show |
10 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1195_96+1199del others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469016 | ||||||
| chr2:68469091 | G | A | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1264G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469091 | |||||||
| chr2:68469145 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+1318A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469145 | |||||||
| chr2:68469287 | A | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1460A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469287 | |||||||
| chr2:68469291 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.96+1464G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469291 | |||||||
| chr2:68469316 | T | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.96+1489T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469316 | |||||||
| chr2:68469325 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1498T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469325 | |||||||
| chr2:68469516 | T | G | 2 | a0003c0003t0004g0113 a0003c0003t0004g0114 |
2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.96+1689T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469516 | |||||||
| chr2:68469599 | G | A | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1772G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469599 | |||||||
| chr2:68469613 | A | T | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+1786A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469613 | |||||||
| chr2:68469816 | A | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+1989A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469816 | |||||||
| chr2:68469999 | G | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+2172G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469999 | |||||||
| chr2:68470463 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+2636A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470463 | |||||||
| chr2:68470521 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+2694G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470521 | |||||||
| chr2:68470559 | G | A | 37 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(34): Show |
40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.96+2732G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470559 | |||||||
| chr2:68470571 | C | T | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2744C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470571 | |||||||
| chr2:68470623 | A | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+2796A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470623 | |||||||
| chr2:68470667 | A | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+2840A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470667 | |||||||
| chr2:68470846 | C | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0116 others(1): Show |
6 | HG01071.hp1 HG01106.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+3019C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470846 | |||||||
| chr2:68471124 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3297G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471124 | |||||||
| chr2:68471144 | C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+3317C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471144 | |||||||
| chr2:68471278 | T | TAAG | 58 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(55): Show |
61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+3451_96+3452ins others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471278 | |||||||
| chr2:68471339 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+3512G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471339 | |||||||
| chr2:68471396 | G | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3569G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471396 | |||||||
| chr2:68471408 | G | A | 1 | a0004c0004t0003g0014 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.96+3581G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471408 | |||||||
| chr2:68471445 | T | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3618T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471445 | |||||||
| chr2:68471460 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3633A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471460 | |||||||
| chr2:68471520 | C | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3693C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471520 | |||||||
| chr2:68471853 | G | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4026G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471853 | |||||||
| chr2:68471886 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4059C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471886 | |||||||
| chr2:68471947 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+4120A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471947 | |||||||
| chr2:68472163 | G | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4336G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472163 | |||||||
| chr2:68472291 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4464G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472291 | |||||||
| chr2:68472328 | G | A | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.96+4501G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472328 | |||||||
| chr2:68472392 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+4565C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472392 | |||||||
| chr2:68472408 | A | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+4581A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472408 | |||||||
| chr2:68472518 | A | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4691A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472518 | |||||||
| chr2:68472520 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4693A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472520 | |||||||
| chr2:68472809 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4982G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472809 | |||||||
| chr2:68473073 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+5246C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473073 | |||||||
| chr2:68473134 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5307G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473134 | |||||||
| chr2:68473159 | T | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5332T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473159 | |||||||
| chr2:68473194 | G | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+5367G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473194 | |||||||
| chr2:68473271 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+5444T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473271 | |||||||
| chr2:68473284 | C | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+5457C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473284 | |||||||
| chr2:68473298 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5471C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473298 | |||||||
| chr2:68473418 | G | C | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.96+5591G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473418 | |||||||
| chr2:68473441 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5614A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473441 | |||||||
| chr2:68473462 | A | G | 2 | a0002c0002t0010g0167 a0002c0002t0010g0168 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.96+5635A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473462 | |||||||
| chr2:68473488 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5661G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473488 | |||||||
| chr2:68473518 | A | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+5691A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473518 | |||||||
| chr2:68473591 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.96+5764A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473591 | |||||||
| chr2:68473719 | G | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+5892G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473719 | |||||||
| chr2:68473868 | A | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+6041A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473868 | |||||||
| chr2:68474019 | G | A | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+6192G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474019 | |||||||
| chr2:68474032 | C | T | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+6205C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474032 | |||||||
| chr2:68474059 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96+6232G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474059 | |||||||
| chr2:68474094 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.96+6267T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474094 | |||||||
| chr2:68474203 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+6376C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474203 | |||||||
| chr2:68474210 | G | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+6383G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474210 | |||||||
| chr2:68474212 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6385A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474212 | |||||||
| chr2:68474213 | G | GGGCGGGG others(74): Show |
1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6386_96+6387ins others(81): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474213 | |||||||
| chr2:68474215 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6388T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474215 | |||||||
| chr2:68474216 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6389T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474216 | |||||||
| chr2:68474217 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6390T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474217 | |||||||
| chr2:68474228 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6401T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474228 | |||||||
| chr2:68474233 | TTTGGGTT others(70): Show |
T | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6407_96+6483del others(77): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474233 | |||||||
| chr2:68474396 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.96+6569C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474396 | |||||||
| chr2:68474707 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.96+6880T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474707 | |||||||
| chr2:68474740 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+6913C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474740 | |||||||
| chr2:68474754 | T | C | 44 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(41): Show |
47 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.96+6927T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474754 | |||||||
| chr2:68474829 | C | T | 5 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+7002C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474829 | |||||||
| chr2:68474834 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7007G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474834 | |||||||
| chr2:68474858 | C | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7031C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474858 | |||||||
| chr2:68474928 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+7101A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474928 | |||||||
| chr2:68474968 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7141A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474968 | |||||||
| chr2:68475014 | C | T | 1 | a0002c0002t0010g0166 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96+7187C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475014 | |||||||
| chr2:68475146 | G | C | 1 | a0002c0002t0002g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.96+7319G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475146 | |||||||
| chr2:68475276 | G | A | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+7449G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475276 | |||||||
| chr2:68475306 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.96+7479G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475306 | |||||||
| chr2:68475588 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7761G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475588 | |||||||
| chr2:68475634 | T | C | 24 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(21): Show |
26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.96+7807T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475634 | |||||||
| chr2:68475673 | C | T | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+7846C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475673 | |||||||
| chr2:68475821 | G | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7994G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475821 | |||||||
| chr2:68475823 | C | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7996C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475823 | |||||||
| chr2:68475881 | T | TTATATA | 18 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(15): Show |
19 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+8066_96+8071dup others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | ||||||
| chr2:68475881 | T | TTATATAT others(1): Show |
3 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0041 |
3 | HG02886.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.96+8064_96+8071dup others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | ||||||
| chr2:68475881 | T | TTATATAT others(3): Show |
1 | a0002c0002t0002g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.96+8062_96+8071dup others(10): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | ||||||
| chr2:68475881 | T | TTATATAT others(7): Show |
1 | a0006c0007t0006g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.96+8058_96+8071dup others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | ||||||
| chr2:68475881 | T | TTATATAT others(13): Show |
1 | a0006c0007t0006g0002 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+8071_96+8072ins others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | ||||||
| chr2:68475891 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+8064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475891 | |||||||
| chr2:68476122 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+8295G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476122 | |||||||
| chr2:68476158 | G | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8331G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476158 | |||||||
| chr2:68476234 | C | T | 1 | a0002c0002t0008g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.96+8407C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476234 | |||||||
| chr2:68476240 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8413C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476240 | |||||||
| chr2:68476255 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8428A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476255 | |||||||
| chr2:68476271 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8444A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476271 | |||||||
| chr2:68476305 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+8478G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476305 | |||||||
| chr2:68476366 | T | C | 57 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(54): Show |
60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.96+8539T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476366 | |||||||
| chr2:68476371 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+8544T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476371 | |||||||
| chr2:68476476 | C | CA | 17 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0071 others(14): Show |
17 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.96+8669dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68476476 | ||||||
| chr2:68476476 | CA | C | 41 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0065 others(38): Show |
44 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.96+8669delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68476476 | ||||||
| chr2:68476554 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+8727A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476554 | |||||||
| chr2:68476565 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.96+8738A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476565 | |||||||
| chr2:68476585 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8758A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476585 | |||||||
| chr2:68476652 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+8825G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476652 | |||||||
| chr2:68476698 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8871A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476698 | |||||||
| chr2:68476832 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+9005T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476832 | |||||||
| chr2:68476880 | C | T | 1 | a0002c0002t0008g0025 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.96+9053C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476880 | |||||||
| chr2:68476992 | T | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+9165T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476992 | |||||||
| chr2:68477093 | A | C | 1 | a0002c0002t0008g0025 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.96+9266A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477093 | |||||||
| chr2:68477104 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+9277C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477104 | |||||||
| chr2:68477111 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+9284A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477111 | |||||||
| chr2:68477152 | GAT | G | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.96+9328_96+9329del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68477152 | ||||||
| chr2:68477709 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+9882T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477709 | |||||||
| chr2:68477766 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+9939A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477766 | |||||||
| chr2:68477773 | G | A | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+9946G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477773 | |||||||
| chr2:68477948 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+10121A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477948 | |||||||
| chr2:68477998 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+10171A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477998 | |||||||
| chr2:68478017 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+10190G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478017 | |||||||
| chr2:68478149 | G | A | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+10322G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478149 | |||||||
| chr2:68478224 | GAT | G | 2 | a0002c0002t0012g0022 a0012c0015t0013g0164 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.96+10398_96+10399d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478224 | |||||||
| chr2:68478268 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.96+10441A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478268 | |||||||
| chr2:68478291 | A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+10464A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478291 | |||||||
| chr2:68478315 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+10488A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478315 | |||||||
| chr2:68478520 | C | G | 58 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(55): Show |
61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+10693C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478520 | |||||||
| chr2:68478529 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.96+10702A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478529 | |||||||
| chr2:68478711 | C | T | 1 | a0001c0009t0001g0154 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.96+10884C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478711 | |||||||
| chr2:68478804 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+10977T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478804 | |||||||
| chr2:68478887 | G | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+11060G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478887 | |||||||
| chr2:68478888 | A | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+11061A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478888 | |||||||
| chr2:68478889 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.96+11062A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478889 | |||||||
| chr2:68479244 | C | T | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-10946C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479244 | |||||||
| chr2:68479270 | A | G | 1 | a0003c0003t0004g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.97-10920A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479270 | |||||||
| chr2:68479348 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-10842T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479348 | |||||||
| chr2:68479374 | C | G | 1 | a0005c0005t0001g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-10816C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479374 | |||||||
| chr2:68479378 | G | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-10812G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479378 | |||||||
| chr2:68479441 | C | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-10749C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479441 | |||||||
| chr2:68479449 | A | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10741A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479449 | |||||||
| chr2:68479523 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10667G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479523 | |||||||
| chr2:68479591 | G | C | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.97-10599G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479591 | |||||||
| chr2:68479857 | T | C | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.97-10333T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479857 | |||||||
| chr2:68479915 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-10275A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479915 | |||||||
| chr2:68479964 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-10226C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479964 | |||||||
| chr2:68479969 | G | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-10221G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479969 | |||||||
| chr2:68480147 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 |
4 | HG01071.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-10043A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480147 | |||||||
| chr2:68480160 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10030C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480160 | |||||||
| chr2:68480300 | T | G | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.97-9890T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480300 | |||||||
| chr2:68480301 | CCTTTTTT others(7): Show |
C | 2 | a0002c0002t0012g0022 a0012c0015t0013g0164 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-9888_97-9875del others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480301 | |||||||
| chr2:68480307 | T | C | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9883T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480307 | |||||||
| chr2:68480449 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-9741G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480449 | |||||||
| chr2:68480597 | C | T | 1 | a0003c0003t0004g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97-9593C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480597 | |||||||
| chr2:68480619 | T | G | 4 | a0007c0006t0001g0135 a0007c0006t0001g0138 a0007c0006t0001g0139 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9571T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480619 | |||||||
| chr2:68480691 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-9499C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480691 | |||||||
| chr2:68480857 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0079 |
2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.97-9333T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480857 | |||||||
| chr2:68480981 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-9209A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480981 | |||||||
| chr2:68481017 | A | AT | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-9166dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481017 | ||||||
| chr2:68481112 | G | A | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9078G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481112 | |||||||
| chr2:68481185 | A | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.97-9005A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481185 | |||||||
| chr2:68481289 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97-8901C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481289 | |||||||
| chr2:68481293 | T | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8897T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481293 | |||||||
| chr2:68481361 | A | AGTTTT | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
166 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(163): Show |
intron_variant | MODIFIER | c.97-8808_97-8804dup others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481361 | ||||||
| chr2:68481361 | AGTTTT | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-8808_97-8804del others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481361 | ||||||
| chr2:68481504 | TTGA | T | 3 | a0003c0003t0004g0113 a0003c0003t0004g0114 a0003c0003t0004g0123 |
3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.97-8681_97-8679del others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481504 | ||||||
| chr2:68481543 | G | A | 1 | a0002c0002t0007g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97-8647G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481543 | |||||||
| chr2:68481568 | A | G | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-8622A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481568 | |||||||
| chr2:68481662 | G | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-8528G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481662 | |||||||
| chr2:68481675 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-8515A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481675 | |||||||
| chr2:68481752 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8438C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481752 | |||||||
| chr2:68482027 | A | G | 1 | a0004c0004t0003g0021 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.97-8163A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482027 | |||||||
| chr2:68482046 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-8144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482046 | |||||||
| chr2:68482094 | CT | C | 53 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(50): Show |
56 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.97-8085delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68482094 | ||||||
| chr2:68482104 | T | G | 1 | a0001c0001t0011g0070 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97-8086T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482104 | |||||||
| chr2:68482146 | T | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8044T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482146 | |||||||
| chr2:68482458 | G | A | 1 | a0004c0004t0003g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-7732G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482458 | |||||||
| chr2:68482484 | C | T | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-7706C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482484 | |||||||
| chr2:68482499 | C | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97-7691C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482499 | |||||||
| chr2:68482847 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.97-7343G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482847 | |||||||
| chr2:68482876 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97-7314G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482876 | |||||||
| chr2:68483369 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-6821C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483369 | |||||||
| chr2:68483371 | A | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-6819A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483371 | |||||||
| chr2:68483547 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6643A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483547 | |||||||
| chr2:68483752 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6438A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483752 | |||||||
| chr2:68483756 | T | TA | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-6428dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68483756 | ||||||
| chr2:68483798 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-6392A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483798 | |||||||
| chr2:68483815 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97-6375G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483815 | |||||||
| chr2:68483870 | C | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-6320C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483870 | |||||||
| chr2:68483932 | A | G | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6258A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483932 | |||||||
| chr2:68483961 | G | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-6229G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483961 | |||||||
| chr2:68484143 | A | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-6047A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484143 | |||||||
| chr2:68484168 | T | TAACA | 57 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(54): Show |
60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.97-6021_97-6018dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484168 | ||||||
| chr2:68484301 | A | G | 20 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-5889A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484301 | |||||||
| chr2:68484316 | A | G | 2 | a0004c0004t0003g0015 a0004c0004t0003g0020 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.97-5874A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484316 | |||||||
| chr2:68484340 | A | G | 2 | a0002c0002t0012g0022 a0012c0015t0013g0164 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-5850A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484340 | |||||||
| chr2:68484553 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-5637A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484553 | |||||||
| chr2:68484572 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-5618A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484572 | |||||||
| chr2:68484584 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-5606C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484584 | |||||||
| chr2:68484678 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-5512C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484678 | |||||||
| chr2:68484691 | G | GA | 52 | a0001c0001t0001g0098 a0002c0002t0002g0034 a0002c0002t0002g0035 others(49): Show |
55 | HG00738.hp2 HG01109.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.97-5482dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484691 | ||||||
| chr2:68484749 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-5441C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484749 | |||||||
| chr2:68484802 | G | T | 1 | a0004c0004t0003g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.97-5388G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484802 | |||||||
| chr2:68484964 | C | CTG | 31 | a0001c0001t0001g0100 a0002c0002t0002g0034 a0002c0002t0002g0035 others(28): Show |
33 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-5209_97-5208dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484964 | ||||||
| chr2:68484964 | C | CTGTG | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-5211_97-5208dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484964 | ||||||
| chr2:68484981 | T | TGC | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-5206_97-5205dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484981 | ||||||
| chr2:68485157 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-5033C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485157 | |||||||
| chr2:68485171 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-5019G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485171 | |||||||
| chr2:68485202 | A | T | 1 | a0003c0003t0004g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-4988A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485202 | |||||||
| chr2:68485325 | A | C | 2 | a0002c0002t0012g0022 a0012c0015t0013g0164 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-4865A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485325 | |||||||
| chr2:68485563 | A | G | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-4627A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485563 | |||||||
| chr2:68485586 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-4604T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485586 | |||||||
| chr2:68485616 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-4574C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485616 | |||||||
| chr2:68485666 | G | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-4524G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485666 | |||||||
| chr2:68485780 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.97-4410T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485780 | |||||||
| chr2:68485809 | C | CT | 6 | a0001c0001t0001g0112 a0001c0009t0001g0154 a0003c0003t0004g0103 others(3): Show |
6 | HG00673.hp2 HG01243.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-4363dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | ||||||
| chr2:68485809 | CT | C | 50 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(47): Show |
53 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.97-4363delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | ||||||
| chr2:68485809 | CTT | C | 5 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(2): Show |
5 | HG01433.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-4364_97-4363del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | ||||||
| chr2:68485811 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.97-4379T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485811 | |||||||
| chr2:68485873 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0002c0002t0008g0024 others(2): Show |
5 | HG01167.hp2 HG02055.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-4317G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485873 | |||||||
| chr2:68486094 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-4096T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486094 | |||||||
| chr2:68486108 | C | G | 1 | a0004c0004t0003g0014 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.97-4082C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486108 | |||||||
| chr2:68486121 | G | T | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-4069G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486121 | |||||||
| chr2:68486225 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-3965G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486225 | |||||||
| chr2:68486289 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-3901A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486289 | |||||||
| chr2:68486389 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-3801C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486389 | |||||||
| chr2:68486527 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-3663C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486527 | |||||||
| chr2:68486763 | AATT | A | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3423_97-3421del others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68486763 | ||||||
| chr2:68486807 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-3383G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486807 | |||||||
| chr2:68487151 | C | T | 1 | a0004c0004t0003g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.97-3039C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487151 | |||||||
| chr2:68487212 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-2978T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487212 | |||||||
| chr2:68487249 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.97-2941A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487249 | |||||||
| chr2:68487416 | T | C | 24 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(21): Show |
26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.97-2774T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487416 | |||||||
| chr2:68487435 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01169.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.97-2755G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487435 | |||||||
| chr2:68487528 | A | C | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-2662A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487528 | |||||||
| chr2:68488018 | GCTTA | G | 37 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(34): Show |
40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-2168_97-2165del others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488018 | ||||||
| chr2:68488098 | G | T | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-2092G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488098 | |||||||
| chr2:68488329 | CT | C | 47 | a0001c0001t0001g0106 a0002c0002t0002g0034 a0002c0002t0002g0035 others(44): Show |
49 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.97-1842delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488329 | ||||||
| chr2:68488329 | CTT | C | 6 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(3): Show |
7 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-1843_97-1842del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488329 | ||||||
| chr2:68488334 | T | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-1856T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488334 | |||||||
| chr2:68488573 | G | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-1617G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488573 | |||||||
| chr2:68488729 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1461T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488729 | |||||||
| chr2:68488976 | A | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-1214A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488976 | |||||||
| chr2:68489076 | T | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-1114T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489076 | |||||||
| chr2:68489108 | A | G | 1 | a0003c0003t0004g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-1082A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489108 | |||||||
| chr2:68489173 | G | A | 1 | a0003c0003t0005g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-1017G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489173 | |||||||
| chr2:68489402 | A | G | 1 | a0004c0004t0003g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-788A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489402 | |||||||
| chr2:68489567 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-623A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489567 | |||||||
| chr2:68489569 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0081 others(1): Show |
4 | HG00741.hp1 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-621G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489569 | |||||||
| chr2:68489742 | C | T | 1 | a0003c0003t0004g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97-448C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489742 | |||||||
| chr2:68489869 | G | C | 75 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(72): Show |
78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-321G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489869 | |||||||
| chr2:68489930 | C | T | 1 | a0003c0003t0004g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.97-260C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489930 | |||||||
| chr2:68489950 | G | A | 2 | a0002c0002t0002g0046 a0002c0002t0002g0047 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.97-240G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489950 | |||||||
| chr2:68490010 | T | A | 22 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(19): Show |
22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-180T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490010 | |||||||
| chr2:68490014 | C | CTCTGAGT others(1): Show |
2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-174_97-173insTG others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68490014 | ||||||
| chr2:68490052 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-138C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490052 | |||||||
| chr2:68490059 | T | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-131T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490059 | |||||||
| chr2:68490107 | G | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-83G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490107 | |||||||
| chr2:68490367 | A | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+106A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490367 | |||||||
| chr2:68490551 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.168+290A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490551 | |||||||
| chr2:68490710 | T | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+449T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490710 | |||||||
| chr2:68490846 | G | A | 1 | a0002c0002t0006g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+585G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490846 | |||||||
| chr2:68491059 | G | C | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.168+798G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491059 | |||||||
| chr2:68491072 | G | A | 2 | a0003c0003t0004g0113 a0003c0003t0004g0114 |
2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.168+811G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491072 | |||||||
| chr2:68491101 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.168+840T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491101 | |||||||
| chr2:68491725 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1464C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491725 | |||||||
| chr2:68491727 | G | A | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.168+1466G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491727 | |||||||
| chr2:68491890 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0064 others(28): Show |
33 | HG00323.hp1 HG00323.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.168+1629T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491890 | |||||||
| chr2:68492154 | A | C | 1 | a0002c0002t0002g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+1893A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492154 | |||||||
| chr2:68492244 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+1983C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492244 | |||||||
| chr2:68492244 | CG | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1987delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68492244 | ||||||
| chr2:68492249 | T | C | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.168+1988T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492249 | |||||||
| chr2:68492281 | A | G | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+2020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492281 | |||||||
| chr2:68492282 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+2021T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492282 | |||||||
| chr2:68492313 | C | T | 19 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+2052C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492313 | |||||||
| chr2:68492338 | C | T | 2 | a0003c0003t0004g0113 a0003c0003t0004g0114 |
2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.168+2077C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492338 | |||||||
| chr2:68492388 | G | T | 20 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+2127G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492388 | |||||||
| chr2:68492403 | G | A | 20 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+2142G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492403 | |||||||
| chr2:68492457 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+2196G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492457 | |||||||
| chr2:68492560 | C | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(30): Show |
35 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.168+2299C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492560 | |||||||
| chr2:68492666 | C | T | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+2405C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492666 | |||||||
| chr2:68492702 | C | A | 2 | a0002c0002t0012g0022 a0003c0003t0005g0127 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+2441C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492702 | |||||||
| chr2:68492826 | T | A | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2565T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492826 | |||||||
| chr2:68492959 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.168+2698A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492959 | |||||||
| chr2:68492987 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492987 | |||||||
| chr2:68493016 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.168+2755A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493016 | |||||||
| chr2:68493061 | T | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+2800T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493061 | |||||||
| chr2:68493101 | A | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+2840A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493101 | |||||||
| chr2:68493327 | G | GA | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3075dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68493327 | ||||||
| chr2:68493334 | A | C | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3073A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493334 | |||||||
| chr2:68493609 | C | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3348C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493609 | |||||||
| chr2:68493613 | A | G | 3 | a0002c0002t0012g0022 a0003c0003t0005g0127 a0012c0015t0013g0164 |
3 | HG02572.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.168+3352A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493613 | |||||||
| chr2:68493825 | G | A | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3564G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493825 | |||||||
| chr2:68493846 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+3585C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493846 | |||||||
| chr2:68493890 | C | T | 24 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(21): Show |
26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.168+3629C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493890 | |||||||
| chr2:68493935 | C | T | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+3674C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493935 | |||||||
| chr2:68493967 | G | A | 11 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+3706G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493967 | |||||||
| chr2:68494113 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+3852A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494113 | |||||||
| chr2:68494207 | G | T | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3946G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494207 | |||||||
| chr2:68494277 | C | CA | 25 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0066 others(22): Show |
25 | HG00323.hp1 HG00673.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.168+4041dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | ||||||
| chr2:68494277 | C | CAA | 5 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0081 others(2): Show |
5 | HG00741.hp1 HG01433.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+4040_168+4041d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | ||||||
| chr2:68494277 | CA | C | 39 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(36): Show |
41 | HG01167.hp2 HG01243.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.168+4041delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | ||||||
| chr2:68494277 | CAAAAAAA others(4): Show |
C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4031_168+4041d others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | ||||||
| chr2:68494277 | CAAAAAAA others(6): Show |
C | 1 | a0007c0006t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.168+4029_168+4041d others(15): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | ||||||
| chr2:68494280 | A | C | 1 | a0002c0002t0008g0024 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.168+4019A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494280 | |||||||
| chr2:68494281 | A | C | 2 | a0002c0002t0008g0025 a0002c0002t0008g0026 |
2 | HG01167.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.168+4020A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494281 | |||||||
| chr2:68494309 | A | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4048A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494309 | |||||||
| chr2:68494337 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+4076G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494337 | |||||||
| chr2:68494362 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+4101A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494362 | |||||||
| chr2:68494530 | G | C | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.168+4269G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494530 | |||||||
| chr2:68494649 | C | T | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+4388C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494649 | |||||||
| chr2:68494691 | T | A | 9 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+4430T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494691 | |||||||
| chr2:68494820 | A | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+4559A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494820 | |||||||
| chr2:68494844 | C | T | 58 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(55): Show |
61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.168+4583C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494844 | |||||||
| chr2:68494876 | A | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4615A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494876 | |||||||
| chr2:68494895 | G | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+4634G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494895 | |||||||
| chr2:68494900 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+4639T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494900 | |||||||
| chr2:68494975 | C | T | 1 | a0004c0004t0003g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+4714C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494975 | |||||||
| chr2:68495063 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+4802A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495063 | |||||||
| chr2:68495389 | C | T | 20 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+5128C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495389 | |||||||
| chr2:68495394 | G | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5133G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495394 | |||||||
| chr2:68495465 | C | A | 75 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(72): Show |
78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.168+5204C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495465 | |||||||
| chr2:68495478 | C | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5217C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495478 | |||||||
| chr2:68495577 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5316A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495577 | |||||||
| chr2:68495650 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5389T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495650 | |||||||
| chr2:68495803 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5542T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495803 | |||||||
| chr2:68495822 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+5561G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495822 | |||||||
| chr2:68495868 | G | C | 1 | a0004c0004t0003g0021 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.168+5607G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495868 | |||||||
| chr2:68495885 | G | A | 11 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+5624G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495885 | |||||||
| chr2:68496076 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+5815G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496076 | |||||||
| chr2:68496136 | G | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5875G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496136 | |||||||
| chr2:68496138 | G | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+5877G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496138 | |||||||
| chr2:68496262 | C | T | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+6001C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496262 | |||||||
| chr2:68496263 | G | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+6002G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496263 | |||||||
| chr2:68496395 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+6134G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496395 | |||||||
| chr2:68496461 | G | A | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.168+6200G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496461 | |||||||
| chr2:68496504 | G | A | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-6227G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496504 | |||||||
| chr2:68496524 | T | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-6207T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496524 | |||||||
| chr2:68496607 | G | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-6124G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496607 | |||||||
| chr2:68496675 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169-6056A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496675 | |||||||
| chr2:68496780 | G | A | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-5951G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496780 | |||||||
| chr2:68496781 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-5950A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496781 | |||||||
| chr2:68496997 | C | G | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-5734C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496997 | |||||||
| chr2:68497103 | T | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
9 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-5628T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497103 | |||||||
| chr2:68497149 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5582T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497149 | |||||||
| chr2:68497181 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5550A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497181 | |||||||
| chr2:68497193 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-5538A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497193 | |||||||
| chr2:68497219 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5512T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497219 | |||||||
| chr2:68497488 | CT | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5241delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68497488 | ||||||
| chr2:68497594 | T | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-5137T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497594 | |||||||
| chr2:68497628 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-5103T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497628 | |||||||
| chr2:68497643 | G | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5088G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497643 | |||||||
| chr2:68497702 | C | T | 7 | a0001c0001t0001g0149 a0002c0002t0002g0036 a0002c0002t0002g0037 others(4): Show |
7 | HG00639.hp2 HG01175.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-5029C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497702 | |||||||
| chr2:68497813 | C | A | 22 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(19): Show |
22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.169-4918C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497813 | |||||||
| chr2:68498000 | GTAT | G | 37 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(34): Show |
40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.169-4729_169-4727d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68498000 | ||||||
| chr2:68498044 | C | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4687C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498044 | |||||||
| chr2:68498299 | A | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4432A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498299 | |||||||
| chr2:68498300 | A | G | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-4431A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498300 | |||||||
| chr2:68498308 | G | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4423G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498308 | |||||||
| chr2:68498378 | G | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4353G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498378 | |||||||
| chr2:68498560 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-4171T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498560 | |||||||
| chr2:68499014 | T | TAA | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-3708_169-3707d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499014 | ||||||
| chr2:68499014 | TA | T | 15 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(12): Show |
16 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.169-3707delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499014 | ||||||
| chr2:68499036 | TAAAC | T | 2 | a0004c0004t0003g0010 a0004c0004t0003g0012 |
2 | HG02293.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.169-3683_169-3680d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499036 | ||||||
| chr2:68499170 | A | G | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-3561A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499170 | |||||||
| chr2:68499329 | C | T | 55 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(52): Show |
58 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.169-3402C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499329 | |||||||
| chr2:68499366 | G | A | 2 | a0006c0007t0017g0023 a0006c0013t0016g0165 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169-3365G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499366 | |||||||
| chr2:68499387 | G | A | 56 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(53): Show |
59 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-3344G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499387 | |||||||
| chr2:68499440 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-3291T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499440 | |||||||
| chr2:68499606 | G | A | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
140 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.169-3125G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499606 | |||||||
| chr2:68499711 | C | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-3020C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499711 | |||||||
| chr2:68499724 | A | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-3007A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499724 | |||||||
| chr2:68499927 | G | A | 33 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(30): Show |
36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.169-2804G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499927 | |||||||
| chr2:68500014 | G | A | 57 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(54): Show |
60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.169-2717G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500014 | |||||||
| chr2:68500016 | G | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2715G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500016 | |||||||
| chr2:68500076 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.169-2655T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500076 | |||||||
| chr2:68500386 | T | TTAAA | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-2342_169-2339d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68500386 | ||||||
| chr2:68501085 | T | C | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1646T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501085 | |||||||
| chr2:68501165 | C | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1566C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501165 | |||||||
| chr2:68501165 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-1566C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501165 | |||||||
| chr2:68501180 | G | T | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-1551G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501180 | |||||||
| chr2:68501220 | T | C | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1511T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501220 | |||||||
| chr2:68501351 | G | A | 56 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(53): Show |
59 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-1380G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501351 | |||||||
| chr2:68501371 | T | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.169-1360T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501371 | |||||||
| chr2:68501436 | AAACACC | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-1292_169-1287d others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68501436 | ||||||
| chr2:68501569 | A | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1162A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501569 | |||||||
| chr2:68501590 | A | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-1141A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501590 | |||||||
| chr2:68501641 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169-1090G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501641 | |||||||
| chr2:68501815 | G | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-916G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501815 | |||||||
| chr2:68502166 | C | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169-565C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502166 | |||||||
| chr2:68502166 | C | T | 41 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(38): Show |
43 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.169-565C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502166 | |||||||
| chr2:68502174 | T | C | 2 | a0002c0002t0012g0022 a0003c0003t0005g0127 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-557T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502174 | |||||||
| chr2:68502185 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-546C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502185 | |||||||
| chr2:68502938 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.341+35T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68502938 | |||||||
| chr2:68503179 | G | C | 57 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(54): Show |
60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.341+276G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503179 | |||||||
| chr2:68503294 | T | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.341+391T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503294 | |||||||
| chr2:68503358 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+455G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503358 | |||||||
| chr2:68503451 | T | G | 1 | a0003c0003t0004g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.341+548T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503451 | |||||||
| chr2:68503491 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01243.hp2 HG01891.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+588G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503491 | |||||||
| chr2:68503507 | A | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+604A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503507 | |||||||
| chr2:68503581 | C | T | 55 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(52): Show |
58 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.341+678C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503581 | |||||||
| chr2:68503783 | T | G | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.341+880T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503783 | |||||||
| chr2:68503967 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341+1064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503967 | |||||||
| chr2:68504011 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.341+1108A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504011 | |||||||
| chr2:68504022 | T | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341+1119T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504022 | |||||||
| chr2:68504055 | C | T | 22 | a0002c0002t0012g0022 a0003c0003t0004g0103 a0003c0003t0004g0113 others(19): Show |
22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.341+1152C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504055 | |||||||
| chr2:68504094 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+1191A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504094 | |||||||
| chr2:68504221 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+1318A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504221 | |||||||
| chr2:68504241 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+1338A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504241 | |||||||
| chr2:68504259 | T | C | 1 | a0002c0002t0002g0042 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.341+1356T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504259 | |||||||
| chr2:68504332 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.341+1429A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504332 | |||||||
| chr2:68504451 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+1548C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504451 | |||||||
| chr2:68504576 | T | C | 8 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(5): Show |
8 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+1673T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504576 | |||||||
| chr2:68504628 | CA | C | 30 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(27): Show |
33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.341+1731delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68504628 | ||||||
| chr2:68504799 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+1896A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504799 | |||||||
| chr2:68505004 | C | T | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341+2101C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505004 | |||||||
| chr2:68505186 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(30): Show |
35 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+2283G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505186 | |||||||
| chr2:68505195 | G | A | 2 | a0001c0001t0001g0066 a0010c0014t0009g0032 |
2 | HG02622.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.341+2292G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505195 | |||||||
| chr2:68505298 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+2395A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505298 | |||||||
| chr2:68506239 | T | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+3336T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506239 | |||||||
| chr2:68506257 | T | C | 78 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(75): Show |
81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.341+3354T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506257 | |||||||
| chr2:68506277 | T | TGGGGGCA others(316): Show |
1 | a0002c0002t0002g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.341+3387_341+3388i others(325): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(317): Show |
3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(326): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(318): Show |
5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(327): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(319): Show |
1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.341+3387_341+3388i others(328): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(320): Show |
5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(329): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(328): Show |
2 | a0002c0002t0002g0045 a0002c0002t0002g0048 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(337): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(328): Show |
2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(337): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(329): Show |
9 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0042 others(6): Show |
10 | HG01884.hp2 HG02886.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(338): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(329): Show |
1 | a0002c0002t0002g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.341+3387_341+3388i others(338): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(330): Show |
6 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0039 others(3): Show |
7 | HG01243.hp1 HG01433.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(339): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506277 | T | TGGGGGCA others(331): Show |
3 | a0002c0002t0002g0038 a0002c0002t0002g0052 a0002c0002t0002g0054 |
3 | HG02145.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(340): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | ||||||
| chr2:68506385 | T | G | 8 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(5): Show |
8 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+3482T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506385 | |||||||
| chr2:68506674 | C | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+3771C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506674 | |||||||
| chr2:68506744 | G | A | 2 | a0001c0001t0001g0144 a0001c0009t0001g0154 |
2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.341+3841G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506744 | |||||||
| chr2:68506875 | T | G | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341+3972T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506875 | |||||||
| chr2:68507057 | G | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.341+4154G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507057 | |||||||
| chr2:68507123 | G | A | 1 | a0004c0004t0003g0011 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.341+4220G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507123 | |||||||
| chr2:68507174 | A | G | 8 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(5): Show |
8 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+4271A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507174 | |||||||
| chr2:68507246 | C | G | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+4343C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507246 | |||||||
| chr2:68507843 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+4940T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507843 | |||||||
| chr2:68507861 | T | G | 1 | a0002c0002t0010g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.341+4958T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507861 | |||||||
| chr2:68508012 | T | C | 1 | a0002c0002t0002g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.342-5068T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508012 | |||||||
| chr2:68508106 | A | ATATT | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-4972_342-4971i others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68508106 | ||||||
| chr2:68508204 | G | T | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.342-4876G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508204 | |||||||
| chr2:68508249 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-4831G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508249 | |||||||
| chr2:68508426 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-4654T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508426 | |||||||
| chr2:68508492 | T | C | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-4588T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508492 | |||||||
| chr2:68508513 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-4567A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508513 | |||||||
| chr2:68508586 | G | A | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.342-4494G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508586 | |||||||
| chr2:68508764 | ACAATCCT others(4): Show |
A | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.342-4312_342-4302d others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68508764 | ||||||
| chr2:68508776 | C | A | 39 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-4304C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508776 | |||||||
| chr2:68508802 | T | G | 39 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-4278T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508802 | |||||||
| chr2:68508966 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.342-4114G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508966 | |||||||
| chr2:68509112 | A | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3968A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509112 | |||||||
| chr2:68509120 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3960A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509120 | |||||||
| chr2:68509179 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-3901A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509179 | |||||||
| chr2:68509184 | C | T | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.342-3896C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509184 | |||||||
| chr2:68509401 | G | A | 17 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0071 others(14): Show |
17 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.342-3679G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509401 | |||||||
| chr2:68509470 | C | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-3610C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509470 | |||||||
| chr2:68509501 | G | A | 39 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-3579G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509501 | |||||||
| chr2:68509544 | T | C | 1 | a0003c0003t0004g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342-3536T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509544 | |||||||
| chr2:68509545 | G | A | 1 | a0003c0003t0004g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342-3535G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509545 | |||||||
| chr2:68509602 | A | G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.342-3478A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509602 | |||||||
| chr2:68509617 | G | C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-3463G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509617 | |||||||
| chr2:68509627 | A | T | 1 | a0005c0005t0014g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342-3453A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509627 | |||||||
| chr2:68509768 | C | T | 20 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.342-3312C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509768 | |||||||
| chr2:68509831 | A | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3249A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509831 | |||||||
| chr2:68509860 | T | C | 110 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0064 others(107): Show |
115 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.342-3220T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509860 | |||||||
| chr2:68509861 | G | A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.342-3219G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509861 | |||||||
| chr2:68510081 | G | C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2999G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510081 | |||||||
| chr2:68510123 | C | T | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342-2957C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510123 | |||||||
| chr2:68510188 | G | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.342-2892G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510188 | |||||||
| chr2:68510307 | C | T | 5 | a0004c0004t0003g0014 a0004c0004t0003g0017 a0004c0004t0003g0018 others(2): Show |
5 | NA18943.hp2 NA18966.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-2773C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510307 | |||||||
| chr2:68510324 | C | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.342-2756C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510324 | |||||||
| chr2:68510638 | G | A | 31 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(28): Show |
33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.342-2442G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510638 | |||||||
| chr2:68510745 | C | T | 1 | a0003c0003t0004g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.342-2335C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510745 | |||||||
| chr2:68510776 | T | G | 1 | a0002c0002t0008g0025 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.342-2304T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510776 | |||||||
| chr2:68510835 | T | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.342-2245T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510835 | |||||||
| chr2:68510851 | A | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2229A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510851 | |||||||
| chr2:68510995 | A | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2085A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510995 | |||||||
| chr2:68511030 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-2050A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511030 | |||||||
| chr2:68511199 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.342-1881T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511199 | |||||||
| chr2:68511279 | G | A | 39 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-1801G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511279 | |||||||
| chr2:68511448 | T | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.342-1632T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511448 | |||||||
| chr2:68511458 | C | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-1622C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511458 | |||||||
| chr2:68511488 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.342-1592T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511488 | |||||||
| chr2:68511840 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-1240A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511840 | |||||||
| chr2:68511869 | C | T | 40 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(37): Show |
42 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.342-1211C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511869 | |||||||
| chr2:68511960 | C | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-1120C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511960 | |||||||
| chr2:68512129 | T | C | 1 | a0002c0002t0008g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.342-951T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512129 | |||||||
| chr2:68512154 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.342-926T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512154 | |||||||
| chr2:68512158 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0115 |
2 | NA18962.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.342-922A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512158 | |||||||
| chr2:68512196 | G | C | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-884G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512196 | |||||||
| chr2:68512206 | C | G | 1 | a0002c0002t0007g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342-874C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512206 | |||||||
| chr2:68512259 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-821A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512259 | |||||||
| chr2:68512391 | T | C | 2 | a0004c0004t0003g0015 a0004c0004t0003g0020 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.342-689T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512391 | |||||||
| chr2:68512505 | A | G | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-575A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512505 | |||||||
| chr2:68512661 | A | G | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-419A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512661 | |||||||
| chr2:68512831 | T | C | 1 | a0004c0004t0003g0011 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.342-249T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512831 | |||||||
| chr2:68512869 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342-211G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512869 | |||||||
| chr2:68512926 | G | T | 2 | a0003c0003t0004g0120 a0003c0003t0004g0122 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.342-154G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512926 | |||||||
| chr2:68513003 | T | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-77T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68513003 | |||||||
| chr2:68513387 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(29): Show |
34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.489+160C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513387 | |||||||
| chr2:68513466 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-82G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513466 | |||||||
| chr2:68513469 | A | G | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.490-79A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513469 | |||||||
| chr2:68513470 | G | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-78G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513470 | |||||||
| chr2:68513473 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-75T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513473 | |||||||
| chr2:68513501 | A | G | 1 | a0002c0002t0010g0166 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-47A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513501 | |||||||
| chr2:68513770 | TATAGAG | T | 54 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(51): Show |
56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+97_622+102delA others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513770 | ||||||
| chr2:68513814 | G | GT | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.622+141dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513814 | ||||||
| chr2:68513886 | AT | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+214delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513886 | ||||||
| chr2:68513958 | G | T | 2 | a0004c0004t0003g0015 a0004c0004t0003g0020 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.622+278G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68513958 | |||||||
| chr2:68514034 | T | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+354T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514034 | |||||||
| chr2:68514154 | G | T | 54 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(51): Show |
56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+474G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514154 | |||||||
| chr2:68514264 | C | T | 54 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(51): Show |
56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+584C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514264 | |||||||
| chr2:68514420 | C | T | 1 | a0004c0004t0003g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.622+740C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514420 | |||||||
| chr2:68514508 | G | A | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+828G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514508 | |||||||
| chr2:68514549 | C | T | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+869C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514549 | |||||||
| chr2:68514802 | A | G | 58 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(55): Show |
61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.622+1122A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514802 | |||||||
| chr2:68514828 | C | T | 36 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(33): Show |
38 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.622+1148C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514828 | |||||||
| chr2:68515292 | A | AAT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(29): Show |
34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.622+1630_622+1631d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | ||||||
| chr2:68515292 | AAT | A | 54 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(51): Show |
56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+1630_622+1631d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | ||||||
| chr2:68515292 | AATAT | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+1628_622+1631d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | ||||||
| chr2:68515361 | G | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+1681G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515361 | |||||||
| chr2:68515532 | A | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+1852A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515532 | |||||||
| chr2:68515721 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.622+2041G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515721 | |||||||
| chr2:68515742 | C | G | 1 | a0003c0003t0004g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.622+2062C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515742 | |||||||
| chr2:68515892 | C | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+2212C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515892 | |||||||
| chr2:68516311 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0137 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.622+2631G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516311 | |||||||
| chr2:68516352 | T | G | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.622+2672T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516352 | |||||||
| chr2:68516416 | T | A | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+2736T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516416 | |||||||
| chr2:68516431 | C | T | 22 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(19): Show |
22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.622+2751C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516431 | |||||||
| chr2:68516494 | G | T | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+2814G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516494 | |||||||
| chr2:68516518 | T | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+2838T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516518 | |||||||
| chr2:68516700 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.622+3020T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516700 | |||||||
| chr2:68516813 | T | C | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3133T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516813 | |||||||
| chr2:68516844 | G | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3164G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516844 | |||||||
| chr2:68516896 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+3216A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516896 | |||||||
| chr2:68516912 | T | C | 31 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(28): Show |
33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.622+3232T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516912 | |||||||
| chr2:68516929 | AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0006c0007t0006g0002 others(3): Show |
7 | HG00741.hp1 HG03098.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.622+3269_622+3282d others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516929 | ||||||
| chr2:68516931 | TATATA | T | 2 | a0002c0002t0002g0037 a0002c0002t0002g0038 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+3262_622+3266d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516931 | ||||||
| chr2:68516959 | TATA | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0092 |
2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.622+3286_622+3288d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516959 | ||||||
| chr2:68516985 | T | A | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+3305T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516985 | |||||||
| chr2:68516986 | A | T | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+3306A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516986 | |||||||
| chr2:68516987 | TATA | T | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+3314_622+3316d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516987 | ||||||
| chr2:68517017 | AATAATAT others(8): Show |
A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+3347_622+3361d others(17): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517017 | ||||||
| chr2:68517018 | A | T | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+3338A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517018 | |||||||
| chr2:68517025 | AT | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3347delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517025 | ||||||
| chr2:68517050 | GTTA | G | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3374_622+3376d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517050 | ||||||
| chr2:68517078 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.622+3398A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517078 | |||||||
| chr2:68517083 | GTTA | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3407_622+3409d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517083 | ||||||
| chr2:68517138 | T | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3458T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517138 | |||||||
| chr2:68517167 | C | T | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3487C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517167 | |||||||
| chr2:68517172 | TATA | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+3498_622+3500d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517172 | ||||||
| chr2:68517202 | AAT | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3527_622+3528d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517202 | ||||||
| chr2:68517224 | A | AAATATAT others(21): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0098 |
2 | HG00738.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.622+3644_622+3671d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | ||||||
| chr2:68517224 | AAATATAT others(21): Show |
A | 65 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0071 others(62): Show |
67 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.622+3644_622+3671d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | ||||||
| chr2:68517224 | AAATATAT others(49): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622+3616_622+3671d others(58): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | ||||||
| chr2:68517248 | TATATAAT others(26): Show |
T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+3574_622+3606d others(35): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517248 | ||||||
| chr2:68517261 | AATATATG others(23): Show |
A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+3586_622+3615d others(32): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517261 | ||||||
| chr2:68517315 | T | G | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+3635T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517315 | |||||||
| chr2:68517326 | C | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3646C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517326 | |||||||
| chr2:68517327 | A | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+3647A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517327 | |||||||
| chr2:68517359 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0158 |
2 | NA19005.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.622+3679A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517359 | |||||||
| chr2:68517397 | A | G | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.622+3717A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517397 | |||||||
| chr2:68517409 | C | CTA | 75 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(72): Show |
78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.622+3735_622+3736d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517409 | ||||||
| chr2:68517425 | A | G | 1 | a0001c0001t0015g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.622+3745A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517425 | |||||||
| chr2:68517435 | CTA | C | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+3761_622+3762d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517435 | ||||||
| chr2:68517470 | GTTA | G | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3794_622+3796d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517470 | ||||||
| chr2:68517538 | CAT | C | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+3861_622+3862d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517538 | ||||||
| chr2:68517612 | CTAA | C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+3934_622+3936d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517612 | ||||||
| chr2:68517632 | C | CAAT | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3954_622+3956d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517632 | ||||||
| chr2:68517661 | TAAC | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+3984_622+3986d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517661 | ||||||
| chr2:68517722 | T | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4042T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517722 | |||||||
| chr2:68517762 | A | C | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+4082A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517762 | |||||||
| chr2:68517802 | A | ACAGTAAT others(27): Show |
3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4196_622+4229d others(36): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517802 | ||||||
| chr2:68517802 | A | ACAGTAAT others(61): Show |
1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4162_622+4229d others(70): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517802 | ||||||
| chr2:68517838 | AGTAATAT others(95): Show |
A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+4190_622+4291d others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517838 | ||||||
| chr2:68517951 | A | C | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.622+4271A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517951 | |||||||
| chr2:68517975 | G | A | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+4295G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517975 | |||||||
| chr2:68517988 | AAT | A | 31 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(28): Show |
33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.622+4311_622+4312d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517988 | ||||||
| chr2:68518111 | CAT | C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4435_622+4436d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518111 | ||||||
| chr2:68518129 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.622+4449A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518129 | |||||||
| chr2:68518166 | GTAATA | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4494_622+4498d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518166 | ||||||
| chr2:68518174 | A | C | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.622+4494A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518174 | |||||||
| chr2:68518214 | C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+4534C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518214 | |||||||
| chr2:68518215 | G | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4535G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518215 | |||||||
| chr2:68518279 | TATA | T | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4603_622+4605d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518279 | ||||||
| chr2:68518310 | T | C | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+4630T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518310 | |||||||
| chr2:68518363 | T | C | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+4683T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518363 | |||||||
| chr2:68518376 | CTG | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0100 |
2 | NA18962.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.622+4698_622+4699d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518376 | ||||||
| chr2:68518378 | G | A | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.622+4698G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518378 | |||||||
| chr2:68518404 | A | ATAT | 66 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(63): Show |
68 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.622+4728_622+4730d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518404 | ||||||
| chr2:68518404 | A | ATATTATT others(18): Show |
9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+4730_622+4731i others(27): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518404 | ||||||
| chr2:68518408 | T | TATTATAT others(30): Show |
3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4730_622+4731i others(39): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518408 | ||||||
| chr2:68518408 | T | TATTATAT others(64): Show |
1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4730_622+4731i others(73): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518408 | ||||||
| chr2:68518425 | T | A | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4745T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518425 | |||||||
| chr2:68518444 | T | C | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.622+4764T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518444 | |||||||
| chr2:68518466 | CATATTA | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.622+4790_622+4795d others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518466 | ||||||
| chr2:68518467 | ATAT | A | 4 | a0002c0002t0007g0029 a0002c0002t0007g0030 a0002c0002t0007g0031 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+4790_622+4792d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518467 | ||||||
| chr2:68518478 | A | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4798A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518478 | |||||||
| chr2:68518479 | C | T | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+4799C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518479 | |||||||
| chr2:68518487 | C | T | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+4807C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518487 | |||||||
| chr2:68518513 | A | G | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+4833A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518513 | |||||||
| chr2:68518543 | A | ATATCAAT others(14): Show |
14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4863_622+4864i others(23): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518543 | |||||||
| chr2:68518557 | G | A | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4877G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518557 | |||||||
| chr2:68518581 | A | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4901A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518581 | |||||||
| chr2:68518598 | T | TATA | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4922_622+4924d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518598 | ||||||
| chr2:68518598 | TATAATAT others(25): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.622+4955_622+4986d others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518598 | ||||||
| chr2:68518603 | T | TA | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4924dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518603 | ||||||
| chr2:68518607 | TC | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4928delC | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518607 | |||||||
| chr2:68518611 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4931T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518611 | |||||||
| chr2:68518611 | T | TAATATAT others(22): Show |
20 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(17): Show |
22 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.622+4933_622+4961d others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | ||||||
| chr2:68518611 | T | TAATATAT others(54): Show |
21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4986_622+4987i others(63): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | ||||||
| chr2:68518611 | T | TAATATAT others(22): Show |
21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+4957_622+4958i others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | ||||||
| chr2:68518611 | T | TAATATAT others(19): Show |
1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+4953_622+4954i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | ||||||
| chr2:68518627 | TATA | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0064 others(10): Show |
15 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.622+4954_622+4956d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518627 | ||||||
| chr2:68518637 | T | TATCAATA others(19): Show |
1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+4961_622+4962i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518637 | ||||||
| chr2:68518711 | CAAT | C | 2 | a0001c0001t0001g0088 a0001c0001t0015g0089 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.622+5036_622+5038d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518711 | ||||||
| chr2:68518742 | AT | A | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5063delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518742 | |||||||
| chr2:68518746 | T | A | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5066T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518746 | |||||||
| chr2:68518749 | A | ATATATAA others(19): Show |
1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5083_622+5084i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518749 | ||||||
| chr2:68518754 | T | TC | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5074_622+5075i others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518754 | |||||||
| chr2:68518756 | A | T | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5076A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518756 | |||||||
| chr2:68518760 | A | T | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5080A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518760 | |||||||
| chr2:68518764 | TTAA | T | 3 | a0002c0002t0002g0046 a0002c0002t0002g0047 a0002c0002t0012g0022 |
3 | HG01884.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622+5090_622+5092d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518764 | ||||||
| chr2:68518765 | T | C | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5085T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518765 | |||||||
| chr2:68518767 | A | T | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5087A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518767 | |||||||
| chr2:68518768 | T | G | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5088T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518768 | |||||||
| chr2:68518774 | A | ATCATTAT others(80): Show |
6 | a0003c0003t0005g0104 a0003c0003t0005g0127 a0003c0003t0005g0129 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.622+5120_622+5121i others(89): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518774 | ||||||
| chr2:68518778 | T | TTAA | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5100_622+5101i others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518778 | ||||||
| chr2:68518801 | C | A | 96 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0071 others(93): Show |
99 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.622+5121C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518801 | |||||||
| chr2:68518802 | T | TGTCATTA others(25): Show |
3 | a0003c0003t0004g0113 a0003c0003t0004g0114 a0003c0003t0004g0123 |
3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.622+5122_622+5123i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518802 | |||||||
| chr2:68518805 | C | CATT | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
148 | HG00323.hp1 HG00323.hp2 HG00673.hp1 others(145): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | ||||||
| chr2:68518805 | C | CATTATAT others(25): Show |
4 | a0002c0002t0002g0048 a0006c0007t0006g0002 a0006c0007t0006g0033 others(1): Show |
5 | HG02630.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | ||||||
| chr2:68518805 | C | CATTATAT others(83): Show |
3 | a0003c0003t0005g0126 a0003c0003t0005g0128 a0003c0003t0005g0133 |
3 | HG02965.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.622+5127_622+5128i others(92): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | ||||||
| chr2:68518805 | C | CATTATAT others(54): Show |
9 | a0003c0003t0004g0103 a0003c0003t0004g0118 a0003c0003t0004g0119 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(63): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | ||||||
| chr2:68518805 | C | T | 3 | a0003c0003t0004g0113 a0003c0003t0004g0114 a0003c0003t0004g0123 |
3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.622+5125C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518805 | |||||||
| chr2:68518814 | A | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0063 |
3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622+5134A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518814 | |||||||
| chr2:68518822 | G | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+5142G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518822 | |||||||
| chr2:68518837 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0063 |
3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622+5157T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518837 | |||||||
| chr2:68518861 | G | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+5181G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518861 | |||||||
| chr2:68518886 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+5206A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518886 | |||||||
| chr2:68518891 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.622+5211A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518891 | |||||||
| chr2:68518928 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5248A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518928 | |||||||
| chr2:68518932 | T | G | 1 | a0004c0004t0003g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.622+5252T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518932 | |||||||
| chr2:68518958 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0064 others(11): Show |
16 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.622+5278A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518958 | |||||||
| chr2:68518962 | CATA | C | 2 | a0002c0002t0008g0024 a0002c0002t0008g0026 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+5289_622+5291d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518962 | ||||||
| chr2:68518985 | C | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.622+5305C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518985 | |||||||
| chr2:68518993 | G | GATAATAT others(21): Show |
13 | a0003c0003t0004g0119 a0003c0003t0004g0120 a0003c0003t0004g0121 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.622+5323_622+5350d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518993 | ||||||
| chr2:68518993 | G | GATAATAT others(49): Show |
6 | a0003c0003t0004g0113 a0003c0003t0004g0114 a0003c0003t0005g0104 others(3): Show |
6 | HG01261.hp2 HG01943.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.622+5350_622+5351i others(58): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518993 | ||||||
| chr2:68518997 | ATATAT | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+5321_622+5325d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518997 | ||||||
| chr2:68519003 | T | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5323T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519003 | |||||||
| chr2:68519031 | G | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+5351G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519031 | |||||||
| chr2:68519039 | T | TATAATAA others(22): Show |
20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.622+5395_622+5423d others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | ||||||
| chr2:68519039 | T | TATAATAA others(51): Show |
1 | a0002c0002t0002g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.622+5366_622+5423d others(60): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | ||||||
| chr2:68519039 | T | TATAATAA others(22): Show |
1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+5374_622+5375i others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | ||||||
| chr2:68519045 | A | AAT | 2 | a0003c0003t0004g0103 a0003c0003t0004g0118 |
2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.622+5369_622+5370d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519045 | ||||||
| chr2:68519057 | A | T | 2 | a0003c0003t0004g0103 a0003c0003t0004g0118 |
2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.622+5377A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519057 | |||||||
| chr2:68519068 | A | AATAATAT others(18): Show |
1 | a0003c0003t0004g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.622+5394_622+5395i others(27): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519068 | ||||||
| chr2:68519085 | T | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5405T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519085 | |||||||
| chr2:68519087 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.622+5407A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519087 | |||||||
| chr2:68519094 | T | TATA | 24 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(21): Show |
25 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.622+5421_622+5423d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | ||||||
| chr2:68519094 | T | TATAATAA others(25): Show |
1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5423_622+5424i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | ||||||
| chr2:68519094 | TATA | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+5421_622+5423d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | ||||||
| chr2:68519117 | A | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+5437A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519117 | |||||||
| chr2:68519139 | TTA | T | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5470_622+5471d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519139 | ||||||
| chr2:68519180 | G | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5500G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519180 | |||||||
| chr2:68519237 | ATATAT | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+5563_622+5567d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519237 | ||||||
| chr2:68519267 | ATATAT | A | 22 | a0002c0002t0009g0003 a0003c0003t0004g0103 a0003c0003t0004g0113 others(19): Show |
23 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.622+5593_622+5597d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519267 | ||||||
| chr2:68519464 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+5784A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519464 | |||||||
| chr2:68519709 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.622+6029C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519709 | |||||||
| chr2:68519857 | G | A | 1 | a0002c0002t0008g0025 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.622+6177G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519857 | |||||||
| chr2:68520014 | C | G | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.623-6047C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520014 | |||||||
| chr2:68520143 | T | C | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-5918T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520143 | |||||||
| chr2:68520244 | A | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(29): Show |
34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.623-5817A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520244 | |||||||
| chr2:68520310 | T | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-5751T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520310 | |||||||
| chr2:68520496 | G | A | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.623-5565G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520496 | |||||||
| chr2:68520708 | C | T | 24 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(21): Show |
25 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.623-5353C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520708 | |||||||
| chr2:68520735 | G | A | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.623-5326G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520735 | |||||||
| chr2:68520791 | T | A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623-5270T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520791 | |||||||
| chr2:68520968 | T | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-5093T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520968 | |||||||
| chr2:68521189 | G | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.623-4872G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521189 | |||||||
| chr2:68521263 | A | G | 2 | a0001c0001t0001g0144 a0001c0009t0001g0154 |
2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.623-4798A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521263 | |||||||
| chr2:68521422 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623-4639A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521422 | |||||||
| chr2:68521457 | A | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-4604A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521457 | |||||||
| chr2:68521521 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-4540A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521521 | |||||||
| chr2:68522139 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.623-3922T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522139 | |||||||
| chr2:68522190 | A | G | 47 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(44): Show |
49 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.623-3871A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522190 | |||||||
| chr2:68522200 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.623-3861C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522200 | |||||||
| chr2:68522202 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.623-3859G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522202 | |||||||
| chr2:68522365 | C | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-3696C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522365 | |||||||
| chr2:68522394 | T | C | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.623-3667T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522394 | |||||||
| chr2:68522411 | T | TA | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-3649dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68522411 | ||||||
| chr2:68522594 | A | G | 1 | a0002c0002t0010g0166 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.623-3467A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522594 | |||||||
| chr2:68522714 | C | T | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623-3347C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522714 | |||||||
| chr2:68522716 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-3345T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522716 | |||||||
| chr2:68522915 | A | C | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.623-3146A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522915 | |||||||
| chr2:68523005 | G | T | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.623-3056G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523005 | |||||||
| chr2:68523094 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-2967C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523094 | |||||||
| chr2:68523204 | G | A | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.623-2857G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523204 | |||||||
| chr2:68523315 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623-2746G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523315 | |||||||
| chr2:68523360 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-2701T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523360 | |||||||
| chr2:68523402 | TATACA | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-2653_623-2649d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523402 | ||||||
| chr2:68523493 | A | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2568A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523493 | |||||||
| chr2:68523559 | A | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-2502A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523559 | |||||||
| chr2:68523580 | T | A | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-2481T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523580 | |||||||
| chr2:68523917 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(28): Show |
33 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.623-2144T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523917 | |||||||
| chr2:68523971 | CT | C | 80 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(77): Show |
83 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.623-2088delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523971 | ||||||
| chr2:68523984 | A | AAT | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2068_623-2067d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523984 | ||||||
| chr2:68523994 | T | TA | 2 | a0004c0004t0003g0010 a0004c0004t0003g0012 |
2 | HG02293.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.623-2067_623-2066i others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523994 | |||||||
| chr2:68523995 | T | A | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.623-2066T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523995 | |||||||
| chr2:68524016 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.623-2045G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524016 | |||||||
| chr2:68524293 | A | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-1768A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524293 | |||||||
| chr2:68524446 | G | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1615G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524446 | |||||||
| chr2:68524452 | G | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1609G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524452 | |||||||
| chr2:68524568 | G | T | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.623-1493G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524568 | |||||||
| chr2:68524587 | T | G | 1 | a0002c0002t0008g0024 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623-1474T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524587 | |||||||
| chr2:68524790 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-1271A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524790 | |||||||
| chr2:68524927 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623-1134A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524927 | |||||||
| chr2:68524934 | G | T | 1 | a0002c0002t0002g0042 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.623-1127G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524934 | |||||||
| chr2:68524966 | G | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1095G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524966 | |||||||
| chr2:68525069 | G | A | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-992G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525069 | |||||||
| chr2:68525109 | C | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623-952C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525109 | |||||||
| chr2:68525120 | T | C | 27 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(24): Show |
27 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.623-941T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525120 | |||||||
| chr2:68525250 | T | C | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.623-811T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525250 | |||||||
| chr2:68525251 | G | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623-810G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525251 | |||||||
| chr2:68525509 | T | A | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.623-552T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525509 | |||||||
| chr2:68525512 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-549A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525512 | |||||||
| chr2:68525555 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-506C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525555 | |||||||
| chr2:68525738 | CTTTCTTT others(13): Show |
C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-319_623-300del others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525738 | ||||||
| chr2:68525742 | C | CT | 14 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0003c0003t0005g0104 others(11): Show |
14 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.623-294dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTT | 14 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.623-295_623-294dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(4): Show |
1 | a0002c0002t0002g0034 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.623-304_623-294dup others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(5): Show |
12 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0041 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-305_623-294dup others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(6): Show |
5 | a0002c0002t0002g0037 a0002c0002t0002g0038 a0002c0002t0002g0045 others(2): Show |
5 | HG03453.hp1 HG03516.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-306_623-294dup others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(7): Show |
2 | a0002c0002t0002g0036 a0002c0002t0002g0054 |
2 | HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.623-307_623-294dup others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(9): Show |
1 | a0002c0002t0002g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.623-309_623-294dup others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(16): Show |
1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.623-316_623-294dup others(23): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | CTTTTTTT others(21): Show |
1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.623-294_623-293ins others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | C | T | 6 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-319C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525742 | |||||||
| chr2:68525742 | CT | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(29): Show |
33 | HG00323.hp1 HG00673.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.623-294delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68525742 | CTTTTTTT others(1): Show |
C | 12 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(9): Show |
12 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-301_623-294del others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | ||||||
| chr2:68526003 | A | C | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.623-58A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68526003 | |||||||
| chr2:68526711 | C | T | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+469C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526711 | |||||||
| chr2:68526733 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.804+491G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526733 | |||||||
| chr2:68526750 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+508C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526750 | |||||||
| chr2:68526876 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.804+634C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526876 | |||||||
| chr2:68526901 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.804+659C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526901 | |||||||
| chr2:68526969 | C | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+727C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526969 | |||||||
| chr2:68526973 | A | T | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+731A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526973 | |||||||
| chr2:68527074 | G | A | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.804+832G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527074 | |||||||
| chr2:68527092 | G | A | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.804+850G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527092 | |||||||
| chr2:68527101 | G | T | 28 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(25): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+859G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527101 | |||||||
| chr2:68527142 | C | T | 4 | a0007c0006t0001g0135 a0007c0006t0001g0138 a0007c0006t0001g0139 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+900C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527142 | |||||||
| chr2:68527172 | G | C | 1 | a0002c0002t0010g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804+930G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527172 | |||||||
| chr2:68527316 | C | T | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+1074C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527316 | |||||||
| chr2:68527557 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0063 |
3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.804+1315C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527557 | |||||||
| chr2:68527576 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.804+1334T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527576 | |||||||
| chr2:68527609 | C | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1367C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527609 | |||||||
| chr2:68527610 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0091 others(1): Show |
4 | HG02717.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+1368G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527610 | |||||||
| chr2:68527627 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.804+1385C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527627 | |||||||
| chr2:68527660 | C | T | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+1418C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527660 | |||||||
| chr2:68527704 | G | A | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804+1462G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527704 | |||||||
| chr2:68527747 | C | T | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1505C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527747 | |||||||
| chr2:68527785 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+1543G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527785 | |||||||
| chr2:68527787 | C | T | 4 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 others(1): Show |
4 | HG01167.hp2 HG02055.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1545C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527787 | |||||||
| chr2:68527893 | G | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1651G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527893 | |||||||
| chr2:68527940 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.804+1698C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527940 | |||||||
| chr2:68528011 | C | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.804+1769C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528011 | |||||||
| chr2:68528140 | C | T | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+1898C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528140 | |||||||
| chr2:68528158 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1916A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528158 | |||||||
| chr2:68528345 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+2103G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528345 | |||||||
| chr2:68528613 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0011g0070 |
2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.804+2371G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528613 | |||||||
| chr2:68528638 | G | A | 1 | a0004c0004t0003g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.804+2396G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528638 | |||||||
| chr2:68528754 | A | T | 17 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(14): Show |
17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+2512A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528754 | |||||||
| chr2:68529019 | A | G | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.804+2777A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529019 | |||||||
| chr2:68529164 | A | AG | 28 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(25): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+2929dupG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68529164 | ||||||
| chr2:68529165 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804+2923G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529165 | |||||||
| chr2:68529170 | G | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.804+2928G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529170 | |||||||
| chr2:68529340 | G | A | 3 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0050 |
3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.804+3098G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529340 | |||||||
| chr2:68529348 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.804+3106C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529348 | |||||||
| chr2:68529383 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.804+3141G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529383 | |||||||
| chr2:68529458 | T | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+3216T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529458 | |||||||
| chr2:68529506 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+3264G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529506 | |||||||
| chr2:68529522 | A | T | 1 | a0003c0003t0004g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804+3280A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529522 | |||||||
| chr2:68529722 | G | A | 1 | a0003c0003t0004g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+3480G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529722 | |||||||
| chr2:68529746 | G | T | 1 | a0002c0011t0002g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.804+3504G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529746 | |||||||
| chr2:68529753 | C | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+3511C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529753 | |||||||
| chr2:68529840 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+3598T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529840 | |||||||
| chr2:68529850 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.804+3608G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529850 | |||||||
| chr2:68529871 | G | GGGCCAGA others(23): Show |
1 | a0002c0002t0010g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804+3630_804+3659d others(32): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68529871 | ||||||
| chr2:68529903 | G | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804+3661G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529903 | |||||||
| chr2:68529931 | C | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+3689C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529931 | |||||||
| chr2:68530007 | T | C | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.804+3765T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530007 | |||||||
| chr2:68530008 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+3766C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530008 | |||||||
| chr2:68530009 | G | A | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.804+3767G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530009 | |||||||
| chr2:68530028 | A | G | 1 | a0003c0003t0005g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.804+3786A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530028 | |||||||
| chr2:68530060 | A | G | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.804+3818A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530060 | |||||||
| chr2:68530087 | G | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.804+3845G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530087 | |||||||
| chr2:68530175 | T | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3933T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530175 | |||||||
| chr2:68530327 | C | A | 23 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(20): Show |
24 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+4085C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530327 | |||||||
| chr2:68530460 | C | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+4218C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530460 | |||||||
| chr2:68530592 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.804+4350T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530592 | |||||||
| chr2:68530797 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.804+4555A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530797 | |||||||
| chr2:68530877 | TA | T | 17 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(14): Show |
17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+4644delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68530877 | ||||||
| chr2:68530893 | G | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+4651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530893 | |||||||
| chr2:68530986 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.804+4744C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530986 | |||||||
| chr2:68531048 | A | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.804+4806A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531048 | |||||||
| chr2:68531154 | G | A | 10 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0043 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.804+4912G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531154 | |||||||
| chr2:68531257 | C | T | 34 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(31): Show |
36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.804+5015C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531257 | |||||||
| chr2:68531301 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804+5059A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531301 | |||||||
| chr2:68531459 | C | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.804+5217C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531459 | |||||||
| chr2:68531731 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.804+5489T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531731 | |||||||
| chr2:68531783 | C | T | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+5541C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531783 | |||||||
| chr2:68531872 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.804+5630A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531872 | |||||||
| chr2:68532030 | G | A | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.804+5788G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532030 | |||||||
| chr2:68532106 | C | T | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.805-5766C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532106 | |||||||
| chr2:68532339 | T | G | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-5533T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532339 | |||||||
| chr2:68532448 | C | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-5424C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532448 | |||||||
| chr2:68532482 | T | C | 52 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(49): Show |
54 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.805-5390T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532482 | |||||||
| chr2:68532599 | G | A | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.805-5273G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532599 | |||||||
| chr2:68532623 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.805-5249G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532623 | |||||||
| chr2:68532852 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-5020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532852 | |||||||
| chr2:68532986 | G | A | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4886G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532986 | |||||||
| chr2:68533071 | T | C | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4801T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533071 | |||||||
| chr2:68533181 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-4691G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533181 | |||||||
| chr2:68533274 | T | C | 47 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(44): Show |
49 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.805-4598T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533274 | |||||||
| chr2:68533285 | A | G | 5 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(2): Show |
5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4587A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533285 | |||||||
| chr2:68533405 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.805-4467G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533405 | |||||||
| chr2:68533515 | C | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-4357C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533515 | |||||||
| chr2:68533605 | T | C | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-4267T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533605 | |||||||
| chr2:68534209 | T | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-3663T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534209 | |||||||
| chr2:68534283 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-3589A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534283 | |||||||
| chr2:68534298 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-3574A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534298 | |||||||
| chr2:68534468 | T | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.805-3404T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534468 | |||||||
| chr2:68534622 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-3250C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534622 | |||||||
| chr2:68534771 | T | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-3101T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534771 | |||||||
| chr2:68534861 | G | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.805-3011G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534861 | |||||||
| chr2:68534869 | A | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-3003A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534869 | |||||||
| chr2:68535055 | A | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2817A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535055 | |||||||
| chr2:68535079 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.805-2793A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535079 | |||||||
| chr2:68535127 | G | GT | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2743dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68535127 | ||||||
| chr2:68535274 | A | G | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.805-2598A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535274 | |||||||
| chr2:68535369 | G | A | 26 | a0001c0001t0001g0084 a0003c0003t0004g0103 a0003c0003t0004g0113 others(23): Show |
27 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.805-2503G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535369 | |||||||
| chr2:68535466 | T | G | 2 | a0002c0002t0002g0051 a0002c0002t0002g0053 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.805-2406T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535466 | |||||||
| chr2:68535603 | CT | C | 17 | a0002c0002t0008g0025 a0004c0004t0003g0009 a0004c0004t0003g0010 others(14): Show |
18 | HG01167.hp2 HG02129.hp1 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.805-2254delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68535603 | ||||||
| chr2:68535834 | G | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2038G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535834 | |||||||
| chr2:68535857 | G | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2015G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535857 | |||||||
| chr2:68535943 | A | G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-1929A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535943 | |||||||
| chr2:68536105 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-1767G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536105 | |||||||
| chr2:68536170 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-1702T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536170 | |||||||
| chr2:68536432 | C | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1440C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536432 | |||||||
| chr2:68536470 | C | T | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805-1402C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536470 | |||||||
| chr2:68536514 | T | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-1358T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536514 | |||||||
| chr2:68536562 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.805-1310A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536562 | |||||||
| chr2:68536568 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.805-1304A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536568 | |||||||
| chr2:68536639 | A | T | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-1233A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536639 | |||||||
| chr2:68536721 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.805-1151C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536721 | |||||||
| chr2:68536834 | A | G | 17 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(14): Show |
17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.805-1038A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536834 | |||||||
| chr2:68536913 | T | TATTA | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.805-959_805-958ins others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536913 | |||||||
| chr2:68536925 | G | C | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-947G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536925 | |||||||
| chr2:68536964 | C | T | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.805-908C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536964 | |||||||
| chr2:68537004 | A | G | 1 | a0003c0003t0004g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.805-868A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537004 | |||||||
| chr2:68537057 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.805-815C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537057 | |||||||
| chr2:68537133 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(2): Show |
5 | HG00741.hp1 HG02886.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-739C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537133 | |||||||
| chr2:68537164 | C | CA | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.805-694dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537164 | ||||||
| chr2:68537164 | CA | C | 7 | a0001c0001t0001g0057 a0002c0002t0010g0166 a0002c0002t0010g0167 others(4): Show |
8 | HG02280.hp2 HG02451.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-694delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537164 | ||||||
| chr2:68537221 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537221 | |||||||
| chr2:68537293 | AT | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-575delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537293 | ||||||
| chr2:68537350 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.805-522G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537350 | |||||||
| chr2:68537394 | T | C | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-478T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537394 | |||||||
| chr2:68537414 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.805-458C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537414 | |||||||
| chr2:68537584 | G | T | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-288G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537584 | |||||||
| chr2:68537637 | T | C | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-235T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537637 | |||||||
| chr2:68537655 | C | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-217C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537655 | |||||||
| chr2:68537741 | G | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-131G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537741 | |||||||
| chr2:68537810 | A | T | 1 | a0002c0002t0002g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.805-62A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537810 | |||||||
| chr2:68538361 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1160+134T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538361 | |||||||
| chr2:68538495 | G | A | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1160+268G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538495 | |||||||
| chr2:68538605 | T | TTTAGGTG others(52): Show |
12 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+379_1160+437d others(61): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68538605 | ||||||
| chr2:68538642 | TTGA | T | 28 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(25): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1160+416_1160+418d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538642 | |||||||
| chr2:68538741 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160+514C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538741 | |||||||
| chr2:68538816 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160+589G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538816 | |||||||
| chr2:68538935 | A | G | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160+708A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538935 | |||||||
| chr2:68538973 | A | C | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1160+746A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538973 | |||||||
| chr2:68539118 | A | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1160+891A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539118 | |||||||
| chr2:68539249 | T | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1160+1022T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539249 | |||||||
| chr2:68539260 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1160+1033G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539260 | |||||||
| chr2:68539373 | T | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+1146T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539373 | |||||||
| chr2:68539379 | G | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1160+1152G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539379 | |||||||
| chr2:68539552 | C | A | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1160+1325C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539552 | |||||||
| chr2:68539768 | C | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+1541C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539768 | |||||||
| chr2:68539781 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1160+1554C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539781 | |||||||
| chr2:68539954 | T | A | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160+1727T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539954 | |||||||
| chr2:68540108 | A | G | 5 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(2): Show |
5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160+1881A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540108 | |||||||
| chr2:68540169 | C | T | 1 | a0002c0002t0002g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1160+1942C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540169 | |||||||
| chr2:68540199 | C | T | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1160+1972C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540199 | |||||||
| chr2:68540234 | C | G | 3 | a0003c0003t0004g0113 a0003c0003t0004g0114 a0003c0003t0004g0123 |
3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1160+2007C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540234 | |||||||
| chr2:68540538 | A | G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+2311A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540538 | |||||||
| chr2:68540576 | G | A | 1 | a0002c0002t0002g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1160+2349G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540576 | |||||||
| chr2:68540599 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1160+2372A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540599 | |||||||
| chr2:68540771 | C | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+2544C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540771 | |||||||
| chr2:68540778 | GTGTGTGT others(3): Show |
G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+2569_1160+257 others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68540778 | ||||||
| chr2:68540862 | A | G | 28 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(25): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1160+2635A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540862 | |||||||
| chr2:68540886 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160+2659C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540886 | |||||||
| chr2:68541195 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1160+2968A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541195 | |||||||
| chr2:68541214 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1160+2987T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541214 | |||||||
| chr2:68541339 | TAGA | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+3115_1160+311 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68541339 | ||||||
| chr2:68541354 | G | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+3127G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541354 | |||||||
| chr2:68541386 | C | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
168 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.1160+3159C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541386 | |||||||
| chr2:68541676 | C | T | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+3449C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541676 | |||||||
| chr2:68541735 | A | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161-3452A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541735 | |||||||
| chr2:68541745 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1161-3442T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541745 | |||||||
| chr2:68542014 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-3173A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542014 | |||||||
| chr2:68542135 | ATATAACT | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-3049_1161-304 others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68542135 | ||||||
| chr2:68542233 | A | T | 1 | a0006c0007t0006g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1161-2954A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542233 | |||||||
| chr2:68542253 | C | T | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-2934C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542253 | |||||||
| chr2:68542358 | G | GAAATGAC others(90): Show |
5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-2750_1161-274 others(101): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68542358 | ||||||
| chr2:68542403 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1161-2784A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542403 | |||||||
| chr2:68542415 | T | C | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1161-2772T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542415 | |||||||
| chr2:68542436 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2751G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542436 | |||||||
| chr2:68542597 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2590G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542597 | |||||||
| chr2:68542767 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161-2420A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542767 | |||||||
| chr2:68542789 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1161-2398A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542789 | |||||||
| chr2:68542942 | A | G | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2245A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542942 | |||||||
| chr2:68543072 | T | G | 2 | a0002c0002t0008g0024 a0002c0002t0008g0026 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2115T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543072 | |||||||
| chr2:68543099 | T | G | 22 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-2088T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543099 | |||||||
| chr2:68543144 | A | G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1161-2043A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543144 | |||||||
| chr2:68543348 | C | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1161-1839C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543348 | |||||||
| chr2:68543398 | G | A | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1161-1789G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543398 | |||||||
| chr2:68543436 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1161-1751A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543436 | |||||||
| chr2:68543547 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1161-1640T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543547 | |||||||
| chr2:68543554 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161-1633C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543554 | |||||||
| chr2:68543636 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-1551G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543636 | |||||||
| chr2:68543981 | CT | C | 61 | a0001c0001t0001g0073 a0002c0002t0002g0034 a0002c0002t0002g0035 others(58): Show |
63 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.1161-1188delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68543981 | ||||||
| chr2:68543981 | CTT | C | 17 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(14): Show |
18 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161-1189_1161-118 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68543981 | ||||||
| chr2:68544003 | A | T | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-1184A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544003 | |||||||
| chr2:68544197 | C | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1161-990C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544197 | |||||||
| chr2:68544342 | C | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-845C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544342 | |||||||
| chr2:68544403 | T | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1161-784T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544403 | |||||||
| chr2:68544420 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161-767A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544420 | |||||||
| chr2:68544535 | A | C | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-652A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544535 | |||||||
| chr2:68544583 | T | C | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-604T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544583 | |||||||
| chr2:68544811 | G | T | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1161-376G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544811 | |||||||
| chr2:68544859 | A | G | 1 | a0002c0002t0008g0025 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1161-328A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544859 | |||||||
| chr2:68544863 | A | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1161-324A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544863 | |||||||
| chr2:68545026 | A | G | 1 | a0003c0003t0005g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1161-161A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545026 | |||||||
| chr2:68545043 | A | G | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1161-144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545043 | |||||||
| chr2:68545149 | AT | A | 19 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(16): Show |
19 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1161-28delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68545149 | ||||||
| chr2:68545169 | T | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1161-18T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545169 | |||||||
| chr2:68545619 | T | C | 22 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(19): Show |
23 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1286+307T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68545619 | |||||||
| chr2:68545676 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1286+364A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68545676 | |||||||
| chr2:68546069 | G | T | 14 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(11): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1286+757G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546069 | |||||||
| chr2:68546275 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1286+963T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546275 | |||||||
| chr2:68546416 | T | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+1104T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546416 | |||||||
| chr2:68546491 | T | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+1179T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546491 | |||||||
| chr2:68546676 | A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1286+1364A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546676 | |||||||
| chr2:68546888 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1286+1576G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546888 | |||||||
| chr2:68546941 | G | A | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286+1629G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546941 | |||||||
| chr2:68546968 | A | G | 32 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(29): Show |
33 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1286+1656A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546968 | |||||||
| chr2:68547078 | G | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+1766G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547078 | |||||||
| chr2:68547180 | A | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+1868A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547180 | |||||||
| chr2:68547227 | A | G | 2 | a0002c0002t0006g0160 a0002c0002t0006g0161 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1286+1915A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547227 | |||||||
| chr2:68547303 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+1991C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547303 | |||||||
| chr2:68547410 | A | G | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1286+2098A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547410 | |||||||
| chr2:68547552 | T | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+2240T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547552 | |||||||
| chr2:68547588 | G | C | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+2276G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547588 | |||||||
| chr2:68547675 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1286+2363C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547675 | |||||||
| chr2:68547794 | G | A | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+2482G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547794 | |||||||
| chr2:68547813 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+2501A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547813 | |||||||
| chr2:68547856 | A | G | 1 | a0002c0002t0002g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1286+2544A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547856 | |||||||
| chr2:68547866 | A | G | 1 | a0004c0004t0003g0011 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1286+2554A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547866 | |||||||
| chr2:68548005 | C | G | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+2693C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548005 | |||||||
| chr2:68548205 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+2893A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548205 | |||||||
| chr2:68548545 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1286+3233A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548545 | |||||||
| chr2:68548604 | A | G | 8 | a0004c0004t0003g0014 a0004c0004t0003g0015 a0004c0004t0003g0016 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+3292A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548604 | |||||||
| chr2:68548691 | C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1286+3379C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548691 | |||||||
| chr2:68548833 | AG | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+3522delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548833 | |||||||
| chr2:68548868 | TTCA | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+3560_1286+356 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68548868 | ||||||
| chr2:68549028 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1286+3716T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549028 | |||||||
| chr2:68549448 | T | G | 2 | a0002c0002t0010g0167 a0002c0002t0010g0168 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+4136T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549448 | |||||||
| chr2:68549480 | A | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+4168A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549480 | |||||||
| chr2:68549499 | A | G | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+4187A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549499 | |||||||
| chr2:68549580 | T | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+4268T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549580 | |||||||
| chr2:68549671 | G | A | 1 | a0005c0005t0001g0148 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1286+4359G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549671 | |||||||
| chr2:68549851 | A | G | 1 | a0002c0002t0010g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1286+4539A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549851 | |||||||
| chr2:68549881 | T | C | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+4569T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549881 | |||||||
| chr2:68550161 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+4849A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550161 | |||||||
| chr2:68550235 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+4923A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550235 | |||||||
| chr2:68550292 | C | T | 1 | a0002c0002t0002g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1286+4980C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550292 | |||||||
| chr2:68550389 | G | A | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1286+5077G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550389 | |||||||
| chr2:68550525 | C | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+5213C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550525 | |||||||
| chr2:68550948 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+5636C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550948 | |||||||
| chr2:68550971 | A | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+5659A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550971 | |||||||
| chr2:68551032 | T | G | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1286+5720T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551032 | |||||||
| chr2:68551084 | C | G | 1 | a0004c0004t0003g0011 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1286+5772C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551084 | |||||||
| chr2:68551163 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1286+5851C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551163 | |||||||
| chr2:68551241 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+5929C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551241 | |||||||
| chr2:68551298 | C | G | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+5986C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551298 | |||||||
| chr2:68551345 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+6033A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551345 | |||||||
| chr2:68551383 | T | C | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1286+6071T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551383 | |||||||
| chr2:68551591 | A | ATTC | 23 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0037 others(20): Show |
23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1286+6291_1286+629 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551591 | ||||||
| chr2:68551601 | T | TCCTTC | 2 | a0002c0002t0008g0024 a0002c0002t0008g0026 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+6289_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551601 | |||||||
| chr2:68551603 | C | CTT | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+6307_1286+630 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | ||||||
| chr2:68551603 | C | CTTCT | 13 | a0002c0002t0002g0054 a0002c0002t0009g0003 a0002c0002t0012g0022 others(10): Show |
14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | ||||||
| chr2:68551603 | C | CTTCTT | 8 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | ||||||
| chr2:68551603 | C | CTTT | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+6306_1286+630 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | ||||||
| chr2:68551603 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+6291C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551603 | |||||||
| chr2:68551604 | T | TTCTTC | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551604 | ||||||
| chr2:68551679 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+6367C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551679 | |||||||
| chr2:68551684 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+6372T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551684 | |||||||
| chr2:68551697 | A | G | 1 | a0003c0003t0004g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1286+6385A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551697 | |||||||
| chr2:68551715 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+6403A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551715 | |||||||
| chr2:68551754 | C | CTT | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+6453_1286+645 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551754 | ||||||
| chr2:68551763 | T | C | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+6451T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551763 | |||||||
| chr2:68551811 | C | T | 3 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 |
3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1286+6499C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551811 | |||||||
| chr2:68551851 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+6539A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551851 | |||||||
| chr2:68551944 | T | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+6632T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551944 | |||||||
| chr2:68552224 | A | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+6912A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552224 | |||||||
| chr2:68552335 | T | C | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+7023T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552335 | |||||||
| chr2:68552382 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+7070C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552382 | |||||||
| chr2:68552402 | TAACC | T | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+7093_1286+709 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68552402 | ||||||
| chr2:68552831 | G | A | 1 | a0006c0007t0006g0002 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1286+7519G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552831 | |||||||
| chr2:68552927 | C | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+7615C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552927 | |||||||
| chr2:68553088 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1286+7776C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553088 | |||||||
| chr2:68553175 | TC | T | 4 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+7864delC | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553175 | |||||||
| chr2:68553236 | A | G | 1 | a0002c0002t0002g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1286+7924A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553236 | |||||||
| chr2:68553247 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+7935A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553247 | |||||||
| chr2:68553291 | T | A | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286+7979T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553291 | |||||||
| chr2:68553342 | A | T | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8030A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553342 | |||||||
| chr2:68553392 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(136): Show |
intron_variant | MODIFIER | c.1286+8080C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553392 | |||||||
| chr2:68553446 | GTATAT | G | 16 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1286+8138_1286+814 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68553446 | ||||||
| chr2:68553531 | A | G | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8219A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553531 | |||||||
| chr2:68553603 | C | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+8291C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553603 | |||||||
| chr2:68553791 | ACTTG | A | 5 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0039 others(2): Show |
5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8483_1286+848 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68553791 | ||||||
| chr2:68554086 | A | C | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+8774A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554086 | |||||||
| chr2:68554161 | T | A | 1 | a0005c0005t0014g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1286+8849T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554161 | |||||||
| chr2:68554249 | T | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+8937T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554249 | |||||||
| chr2:68554277 | G | C | 1 | a0005c0005t0014g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1286+8965G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554277 | |||||||
| chr2:68554372 | A | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1286+9060A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554372 | |||||||
| chr2:68554638 | G | GT | 10 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(7): Show |
11 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1286+9340dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68554638 | ||||||
| chr2:68554735 | G | A | 1 | a0002c0002t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+9423G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554735 | |||||||
| chr2:68554739 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+9427A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554739 | |||||||
| chr2:68555037 | T | C | 28 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(25): Show |
29 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1286+9725T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555037 | |||||||
| chr2:68555042 | G | A | 25 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+9730G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555042 | |||||||
| chr2:68555234 | C | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+9922C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555234 | |||||||
| chr2:68555250 | A | G | 95 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(92): Show |
98 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.1286+9938A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555250 | |||||||
| chr2:68555430 | C | T | 1 | a0001c0001t0011g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1286+10118C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555430 | |||||||
| chr2:68555474 | G | A | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+10162G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555474 | |||||||
| chr2:68555536 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+10224A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555536 | |||||||
| chr2:68555605 | A | G | 1 | a0009c0008t0006g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1286+10293A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555605 | |||||||
| chr2:68555631 | A | C | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1286+10319A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555631 | |||||||
| chr2:68555705 | A | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+10393A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555705 | |||||||
| chr2:68556032 | A | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+10720A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556032 | |||||||
| chr2:68556225 | A | T | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+10913A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556225 | |||||||
| chr2:68556356 | A | T | 1 | a0004c0004t0003g0021 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1287-10985A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556356 | |||||||
| chr2:68556608 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-10733A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556608 | |||||||
| chr2:68556722 | A | G | 1 | a0002c0002t0010g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1287-10619A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556722 | |||||||
| chr2:68556813 | G | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-10528G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556813 | |||||||
| chr2:68556832 | G | C | 10 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(7): Show |
11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-10509G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556832 | |||||||
| chr2:68557200 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1287-10141C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557200 | |||||||
| chr2:68557225 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1287-10116T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557225 | |||||||
| chr2:68557258 | G | A | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-10083G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557258 | |||||||
| chr2:68557277 | A | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-10064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557277 | |||||||
| chr2:68557344 | A | G | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-9997A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557344 | |||||||
| chr2:68557538 | A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-9803A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557538 | |||||||
| chr2:68557652 | C | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-9689C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557652 | |||||||
| chr2:68557677 | T | G | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-9664T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557677 | |||||||
| chr2:68557890 | G | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-9451G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557890 | |||||||
| chr2:68557910 | G | GA | 5 | a0001c0001t0001g0067 a0001c0001t0001g0088 a0005c0005t0001g0148 others(2): Show |
5 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-9417dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68557910 | ||||||
| chr2:68557910 | GA | G | 23 | a0002c0002t0007g0030 a0003c0003t0005g0104 a0003c0003t0005g0126 others(20): Show |
23 | HG01109.hp1 HG02129.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1287-9417delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68557910 | ||||||
| chr2:68557925 | T | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-9416T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557925 | |||||||
| chr2:68557938 | T | C | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-9403T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557938 | |||||||
| chr2:68558126 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1287-9215T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558126 | |||||||
| chr2:68558139 | A | T | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-9202A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558139 | |||||||
| chr2:68558211 | G | A | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1287-9130G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558211 | |||||||
| chr2:68558274 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-9067A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558274 | |||||||
| chr2:68558304 | A | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-9037A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558304 | |||||||
| chr2:68558447 | G | A | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-8894G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558447 | |||||||
| chr2:68558486 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-8855T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558486 | |||||||
| chr2:68558734 | G | A | 10 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(7): Show |
11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-8607G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558734 | |||||||
| chr2:68558797 | G | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-8544G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558797 | |||||||
| chr2:68558800 | C | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-8541C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558800 | |||||||
| chr2:68558802 | G | C | 32 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(29): Show |
33 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1287-8539G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558802 | |||||||
| chr2:68558858 | A | G | 32 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(29): Show |
33 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1287-8483A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558858 | |||||||
| chr2:68559238 | T | C | 10 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(7): Show |
11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-8103T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559238 | |||||||
| chr2:68559345 | G | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-7996G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559345 | |||||||
| chr2:68559381 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7960A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559381 | |||||||
| chr2:68559431 | G | A | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1287-7910G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559431 | |||||||
| chr2:68559477 | G | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7864G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559477 | |||||||
| chr2:68559645 | C | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-7696C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559645 | |||||||
| chr2:68559747 | T | C | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1287-7594T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559747 | |||||||
| chr2:68559910 | C | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-7431C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559910 | |||||||
| chr2:68559993 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0079 others(2): Show |
5 | NA18962.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-7348A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559993 | |||||||
| chr2:68560002 | C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-7339C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560002 | |||||||
| chr2:68560043 | G | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7298G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560043 | |||||||
| chr2:68560059 | T | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-7282T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560059 | |||||||
| chr2:68560177 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-7164A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560177 | |||||||
| chr2:68560362 | G | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-6979G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560362 | |||||||
| chr2:68560413 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1287-6928C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560413 | |||||||
| chr2:68560426 | T | TAGAA | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-6913_1287-691 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68560426 | ||||||
| chr2:68560458 | T | G | 6 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(3): Show |
7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-6883T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560458 | |||||||
| chr2:68560612 | C | T | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-6729C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560612 | |||||||
| chr2:68560615 | C | T | 1 | a0003c0003t0005g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1287-6726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560615 | |||||||
| chr2:68560668 | C | T | 1 | a0003c0003t0004g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1287-6673C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560668 | |||||||
| chr2:68560795 | C | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-6546C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560795 | |||||||
| chr2:68560915 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-6426T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560915 | |||||||
| chr2:68560923 | G | A | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-6418G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560923 | |||||||
| chr2:68560955 | C | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-6386C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560955 | |||||||
| chr2:68560989 | ATAT | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-6348_1287-634 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68560989 | ||||||
| chr2:68561162 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-6179A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561162 | |||||||
| chr2:68561170 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-6171A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561170 | |||||||
| chr2:68561269 | A | G | 1 | a0002c0002t0002g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1287-6072A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561269 | |||||||
| chr2:68561382 | A | C | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-5959A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561382 | |||||||
| chr2:68561421 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-5920A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561421 | |||||||
| chr2:68561623 | G | A | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-5718G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561623 | |||||||
| chr2:68561733 | C | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-5608C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561733 | |||||||
| chr2:68562037 | C | T | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-5304C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562037 | |||||||
| chr2:68562137 | G | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-5204G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562137 | |||||||
| chr2:68562150 | G | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-5191G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562150 | |||||||
| chr2:68562289 | A | T | 1 | a0001c0001t0011g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1287-5052A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562289 | |||||||
| chr2:68562324 | A | G | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-5017A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562324 | |||||||
| chr2:68562598 | T | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-4743T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562598 | |||||||
| chr2:68562749 | A | G | 2 | a0001c0001t0001g0144 a0001c0009t0001g0154 |
2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1287-4592A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562749 | |||||||
| chr2:68562784 | A | C | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-4557A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562784 | |||||||
| chr2:68562916 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-4425A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562916 | |||||||
| chr2:68563029 | C | T | 76 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(73): Show |
79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1287-4312C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563029 | |||||||
| chr2:68563135 | T | C | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-4206T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563135 | |||||||
| chr2:68563217 | A | T | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-4124A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563217 | |||||||
| chr2:68563424 | C | T | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-3917C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563424 | |||||||
| chr2:68563440 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1287-3901G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563440 | |||||||
| chr2:68563635 | A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-3706A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563635 | |||||||
| chr2:68563670 | G | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-3671G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563670 | |||||||
| chr2:68563764 | A | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-3577A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563764 | |||||||
| chr2:68563853 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-3488C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563853 | |||||||
| chr2:68563918 | A | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-3423A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563918 | |||||||
| chr2:68564162 | G | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-3179G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564162 | |||||||
| chr2:68564197 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1287-3144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564197 | |||||||
| chr2:68564308 | T | C | 2 | a0002c0002t0002g0046 a0002c0002t0002g0047 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1287-3033T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564308 | |||||||
| chr2:68564335 | A | G | 1 | a0002c0002t0002g0034 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1287-3006A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564335 | |||||||
| chr2:68564392 | A | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-2949A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564392 | |||||||
| chr2:68564496 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-2845A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564496 | |||||||
| chr2:68564509 | A | G | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-2832A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564509 | |||||||
| chr2:68564665 | T | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2676T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564665 | |||||||
| chr2:68564674 | A | G | 1 | a0002c0002t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1287-2667A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564674 | |||||||
| chr2:68564762 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2579A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564762 | |||||||
| chr2:68564830 | G | T | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287-2511G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564830 | |||||||
| chr2:68565028 | T | C | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-2313T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565028 | |||||||
| chr2:68565207 | AG | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-2133delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565207 | |||||||
| chr2:68565321 | A | G | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565321 | |||||||
| chr2:68565322 | A | G | 12 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-2019A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565322 | |||||||
| chr2:68565504 | T | C | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1837T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565504 | |||||||
| chr2:68565508 | C | CAGAT | 8 | a0002c0002t0002g0043 a0002c0002t0002g0050 a0002c0002t0002g0054 others(5): Show |
9 | HG01167.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-1827_1287-182 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | ||||||
| chr2:68565508 | C | CAGATAGA others(1): Show |
22 | a0002c0002t0002g0048 a0002c0002t0006g0160 a0002c0002t0006g0163 others(19): Show |
23 | HG00639.hp1 HG01192.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1287-1831_1287-182 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | ||||||
| chr2:68565508 | C | CAGATAGA others(5): Show |
2 | a0002c0002t0006g0162 a0009c0008t0006g0027 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | ||||||
| chr2:68565508 | C | CAGATAGA others(9): Show |
1 | a0002c0002t0006g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1287-1824_1287-182 others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | ||||||
| chr2:68565514 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1287-1827G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565514 | |||||||
| chr2:68565514 | G | GATAC | 26 | a0001c0001t0001g0067 a0001c0001t0001g0086 a0001c0001t0001g0087 others(23): Show |
26 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1287-1787_1287-178 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | G | GATACATA others(1): Show |
5 | a0001c0001t0001g0136 a0004c0004t0003g0013 a0004c0004t0003g0014 others(2): Show |
5 | HG02630.hp2 HG03942.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-1791_1287-178 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | G | GATACATA others(5): Show |
2 | a0002c0002t0006g0160 a0002c0002t0006g0163 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1287-1795_1287-178 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | G | GATAGATA others(1): Show |
13 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(10): Show |
13 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | G | GATAGATA others(5): Show |
7 | a0002c0002t0002g0035 a0002c0002t0002g0039 a0003c0003t0004g0119 others(4): Show |
7 | HG00738.hp1 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | G | GATAGATA others(9): Show |
2 | a0002c0002t0002g0034 a0002c0002t0002g0041 |
2 | HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565514 | GATAC | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1287-1787_1287-178 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | ||||||
| chr2:68565518 | C | G | 6 | a0002c0002t0002g0052 a0002c0002t0002g0054 a0002c0002t0009g0003 others(3): Show |
7 | HG02145.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1823C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565518 | |||||||
| chr2:68565522 | C | G | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1287-1819C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565522 | |||||||
| chr2:68565558 | G | C | 41 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(38): Show |
43 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1287-1783G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565558 | |||||||
| chr2:68565572 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1287-1769A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565572 | |||||||
| chr2:68565595 | C | A | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1287-1746C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565595 | |||||||
| chr2:68565669 | T | C | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-1672T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565669 | |||||||
| chr2:68565690 | G | A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-1651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565690 | |||||||
| chr2:68565703 | A | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1638A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565703 | |||||||
| chr2:68565720 | T | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-1621T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565720 | |||||||
| chr2:68565789 | G | T | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-1552G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565789 | |||||||
| chr2:68565844 | G | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
166 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(163): Show |
intron_variant | MODIFIER | c.1287-1497G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565844 | |||||||
| chr2:68565942 | G | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-1399G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565942 | |||||||
| chr2:68566289 | C | T | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1052C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566289 | |||||||
| chr2:68566449 | C | T | 1 | a0004c0004t0003g0010 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1287-892C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566449 | |||||||
| chr2:68566457 | G | A | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-884G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566457 | |||||||
| chr2:68566615 | C | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566615 | |||||||
| chr2:68566995 | C | T | 1 | a0002c0002t0002g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1287-346C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566995 | |||||||
| chr2:68567072 | T | C | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1287-269T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68567072 | |||||||
| chr2:68567396 | G | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+9G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567396 | |||||||
| chr2:68567534 | T | TA | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1333+156dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68567534 | ||||||
| chr2:68567665 | A | G | 5 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(2): Show |
5 | HG02129.hp1 HG02293.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333+278A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567665 | |||||||
| chr2:68567693 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1333+306C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567693 | |||||||
| chr2:68567836 | C | T | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+449C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567836 | |||||||
| chr2:68567949 | T | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+562T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567949 | |||||||
| chr2:68568008 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+621C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568008 | |||||||
| chr2:68568019 | C | T | 1 | a0002c0002t0010g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1333+632C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568019 | |||||||
| chr2:68568533 | G | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+1146G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568533 | |||||||
| chr2:68568535 | A | T | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+1148A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568535 | |||||||
| chr2:68568580 | T | C | 1 | a0006c0007t0017g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1333+1193T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568580 | |||||||
| chr2:68568632 | C | G | 1 | a0002c0002t0002g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1333+1245C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568632 | |||||||
| chr2:68568638 | C | T | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1333+1251C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568638 | |||||||
| chr2:68568711 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1333+1324C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568711 | |||||||
| chr2:68568814 | A | C | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+1427A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568814 | |||||||
| chr2:68568876 | A | G | 17 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(14): Show |
17 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1333+1489A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568876 | |||||||
| chr2:68568929 | A | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+1542A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568929 | |||||||
| chr2:68568956 | C | T | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+1569C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568956 | |||||||
| chr2:68569100 | A | T | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1333+1713A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569100 | |||||||
| chr2:68569192 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0011g0070 |
2 | NA18984.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1333+1805A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569192 | |||||||
| chr2:68569201 | G | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+1814G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569201 | |||||||
| chr2:68569486 | A | G | 73 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0037 others(70): Show |
76 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.1333+2099A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569486 | |||||||
| chr2:68569574 | C | T | 1 | a0011c0012t0007g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1333+2187C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569574 | |||||||
| chr2:68569641 | A | AT | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+2254_1333+225 others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569641 | |||||||
| chr2:68569643 | T | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+2256T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569643 | |||||||
| chr2:68569748 | G | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+2361G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569748 | |||||||
| chr2:68569839 | G | A | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333+2452G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569839 | |||||||
| chr2:68570042 | T | C | 41 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(38): Show |
43 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1333+2655T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570042 | |||||||
| chr2:68570233 | T | C | 1 | a0002c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1333+2846T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570233 | |||||||
| chr2:68570285 | TTAA | T | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+2901_1333+290 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68570285 | ||||||
| chr2:68570287 | A | T | 35 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(32): Show |
36 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1333+2900A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570287 | |||||||
| chr2:68570287 | AAT | A | 31 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(28): Show |
33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333+2913_1333+291 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68570287 | ||||||
| chr2:68570288 | A | T | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+2901A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570288 | |||||||
| chr2:68570288 | AT | A | 30 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1333+2902delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570288 | |||||||
| chr2:68570289 | T | A | 18 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(15): Show |
18 | HG02109.hp1 HG02129.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333+2902T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570289 | |||||||
| chr2:68570314 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1333+2927T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570314 | |||||||
| chr2:68570340 | T | C | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+2953T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570340 | |||||||
| chr2:68570437 | C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+3050C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570437 | |||||||
| chr2:68570629 | T | C | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+3242T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570629 | |||||||
| chr2:68570654 | C | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+3267C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570654 | |||||||
| chr2:68570719 | G | A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1333+3332G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570719 | |||||||
| chr2:68570743 | G | T | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+3356G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570743 | |||||||
| chr2:68570799 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1333+3412G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570799 | |||||||
| chr2:68570865 | T | G | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333+3478T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570865 | |||||||
| chr2:68570868 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1333+3481C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570868 | |||||||
| chr2:68570931 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1333+3544G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570931 | |||||||
| chr2:68571094 | C | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+3707C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571094 | |||||||
| chr2:68571254 | C | A | 3 | a0002c0002t0008g0024 a0002c0002t0008g0025 a0002c0002t0008g0026 |
3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1333+3867C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571254 | |||||||
| chr2:68571300 | T | G | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+3913T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571300 | |||||||
| chr2:68571332 | C | A | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1333+3945C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571332 | |||||||
| chr2:68571462 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333+4075A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571462 | |||||||
| chr2:68571462 | A | T | 1 | a0003c0003t0004g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1333+4075A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571462 | |||||||
| chr2:68571576 | C | G | 1 | a0002c0002t0012g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333+4189C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571576 | |||||||
| chr2:68571641 | C | T | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1333+4254C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571641 | |||||||
| chr2:68571646 | A | G | 1 | a0002c0002t0002g0034 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1333+4259A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571646 | |||||||
| chr2:68571684 | A | T | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+4297A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571684 | |||||||
| chr2:68571786 | G | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+4399G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571786 | |||||||
| chr2:68571940 | T | C | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+4553T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571940 | |||||||
| chr2:68571941 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1333+4554G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571941 | |||||||
| chr2:68571951 | A | G | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333+4564A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571951 | |||||||
| chr2:68572063 | A | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+4676A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572063 | |||||||
| chr2:68572087 | A | AGGCTTAG others(10): Show |
11 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0043 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4700_1333+470 others(21): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572087 | |||||||
| chr2:68572089 | A | T | 11 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0043 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4702A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572089 | |||||||
| chr2:68572094 | A | T | 11 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0043 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4707A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572094 | |||||||
| chr2:68572095 | C | T | 11 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0043 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4708C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572095 | |||||||
| chr2:68572170 | T | C | 1 | a0005c0005t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1333+4783T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572170 | |||||||
| chr2:68572272 | T | G | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+4885T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572272 | |||||||
| chr2:68572273 | A | T | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333+4886A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572273 | |||||||
| chr2:68572322 | G | A | 79 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(76): Show |
82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+4935G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572322 | |||||||
| chr2:68572518 | G | C | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1333+5131G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572518 | |||||||
| chr2:68572646 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0015g0089 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1334-5174G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572646 | |||||||
| chr2:68572679 | T | TA | 20 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(17): Show |
20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1334-5133dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68572679 | ||||||
| chr2:68572819 | A | G | 13 | a0004c0004t0003g0009 a0004c0004t0003g0010 a0004c0004t0003g0011 others(10): Show |
13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1334-5001A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572819 | |||||||
| chr2:68572838 | CAACAA | C | 30 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(27): Show |
31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334-4962_1334-495 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68572838 | ||||||
| chr2:68573090 | A | T | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-4730A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573090 | |||||||
| chr2:68573091 | T | C | 2 | a0006c0007t0006g0002 a0006c0007t0006g0033 |
3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-4729T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573091 | |||||||
| chr2:68573113 | T | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0158 |
2 | NA19005.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1334-4707T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573113 | |||||||
| chr2:68573336 | A | G | 4 | a0001c0001t0001g0067 a0005c0005t0001g0148 a0005c0005t0001g0152 others(1): Show |
4 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-4484A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573336 | |||||||
| chr2:68573370 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1334-4450G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573370 | |||||||
| chr2:68573459 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1334-4361G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573459 | |||||||
| chr2:68573569 | A | G | 10 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(7): Show |
11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1334-4251A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573569 | |||||||
| chr2:68573598 | G | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-4222G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573598 | |||||||
| chr2:68573672 | C | CA | 33 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
35 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1334-4129dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573672 | ||||||
| chr2:68573672 | C | CAA | 32 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(29): Show |
32 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1334-4130_1334-412 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573672 | ||||||
| chr2:68573787 | C | T | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1334-4033C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573787 | |||||||
| chr2:68573795 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1334-4025G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573795 | |||||||
| chr2:68573803 | T | C | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-4017T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573803 | |||||||
| chr2:68573880 | GTTTCC | G | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-3935_1334-393 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573880 | ||||||
| chr2:68573917 | C | T | 4 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(1): Show |
5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-3903C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573917 | |||||||
| chr2:68574004 | T | C | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-3816T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574004 | |||||||
| chr2:68574080 | TA | T | 5 | a0001c0001t0001g0116 a0002c0002t0010g0166 a0002c0002t0010g0167 others(2): Show |
5 | HG01169.hp2 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334-3725delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68574080 | ||||||
| chr2:68574142 | A | G | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-3678A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574142 | |||||||
| chr2:68574221 | A | G | 1 | a0002c0002t0002g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1334-3599A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574221 | |||||||
| chr2:68574280 | T | A | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-3540T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574280 | |||||||
| chr2:68574534 | A | G | 17 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(14): Show |
17 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1334-3286A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574534 | |||||||
| chr2:68574572 | G | A | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334-3248G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574572 | |||||||
| chr2:68574706 | C | T | 9 | a0003c0003t0005g0104 a0003c0003t0005g0126 a0003c0003t0005g0127 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1334-3114C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574706 | |||||||
| chr2:68574760 | A | G | 1 | a0002c0002t0002g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1334-3060A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574760 | |||||||
| chr2:68574807 | T | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-3013T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574807 | |||||||
| chr2:68574956 | G | A | 5 | a0002c0002t0002g0040 a0002c0002t0002g0042 a0002c0002t0002g0051 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-2864G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574956 | |||||||
| chr2:68574958 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-2862G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574958 | |||||||
| chr2:68574962 | C | A | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-2858C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574962 | |||||||
| chr2:68574975 | G | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2845G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574975 | |||||||
| chr2:68575135 | T | C | 3 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-2685T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575135 | |||||||
| chr2:68575155 | C | CAGAT | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2663_1334-266 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68575155 | ||||||
| chr2:68575340 | G | A | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-2480G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575340 | |||||||
| chr2:68575683 | A | G | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-2137A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575683 | |||||||
| chr2:68575793 | T | C | 1 | a0006c0013t0016g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1334-2027T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575793 | |||||||
| chr2:68575972 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-1848C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575972 | |||||||
| chr2:68576074 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1334-1746C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576074 | |||||||
| chr2:68576079 | T | C | 21 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(18): Show |
21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1334-1741T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576079 | |||||||
| chr2:68576217 | A | C | 5 | a0002c0002t0007g0001 a0002c0002t0007g0029 a0002c0002t0007g0030 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334-1603A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576217 | |||||||
| chr2:68576300 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0115 |
2 | NA18962.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1334-1520T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576300 | |||||||
| chr2:68576327 | A | G | 21 | a0003c0003t0004g0103 a0003c0003t0004g0113 a0003c0003t0004g0114 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-1493A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576327 | |||||||
| chr2:68576380 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1334-1440C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576380 | |||||||
| chr2:68576991 | G | T | 3 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 |
3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-829G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576991 | |||||||
| chr2:68576993 | T | A | 31 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(28): Show |
32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-827T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576993 | |||||||
| chr2:68576995 | G | A | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-825G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576995 | |||||||
| chr2:68577123 | G | C | 1 | a0012c0015t0013g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-697G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577123 | |||||||
| chr2:68577167 | G | A | 4 | a0002c0002t0010g0166 a0002c0002t0010g0167 a0002c0002t0010g0168 others(1): Show |
4 | HG02451.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-653G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577167 | |||||||
| chr2:68577200 | G | A | 4 | a0006c0007t0006g0002 a0006c0007t0006g0033 a0006c0007t0017g0023 others(1): Show |
5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-620G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577200 | |||||||
| chr2:68577320 | G | C | 1 | a0010c0014t0009g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334-500G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577320 | |||||||
| chr2:68577436 | C | A | 5 | a0002c0002t0006g0160 a0002c0002t0006g0161 a0002c0002t0006g0162 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-384C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577436 |