Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 161 |
| ensemblid | ENSG00000183020.15 |
| hgncid | 562 |
| symbol | AP2A2 |
| name | adaptor related protein complex 2 subunit alpha 2 |
| refseq_nuc | NM_012305.4 |
| refseq_prot | NP_036437.1 |
| ensembl_nuc | ENST00000448903.7 |
| ensembl_prot | ENSP00000413234.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 925870 |
| end | 1012240 |
| strand | + |
| ver | v1.2 |
| region | chr11:925870-1012240 |
| region5000 | chr11:920870-1017240 |
| regionname0 | AP2A2_chr11_925870_1012240 |
| regionname5000 | AP2A2_chr11_920870_1017240 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 939 | 264 | 69 | 52 | 98 | 12 | 31 | 64 | AP2A2_chr11_920870_1017240 | AP2A2 | MPAVS others(934): Show |
chr11 | 920870 | 1017240 |
| a0002 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | MPAVS others(934): Show |
chr11 | 920870 | 1017240 |
| a0003 | 0/0 | 939 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | MPAVS others(934): Show |
chr11 | 920870 | 1017240 |
| a0004 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | MPAVS others(645): Show |
chr11 | 920870 | 1017240 |
| a0005 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | MPAVS others(934): Show |
chr11 | 920870 | 1017240 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2817 | 120 | 22 | 30 | 46 | 9 | 13 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0002 | 1/1 | 2817 | 89 | 23 | 18 | 32 | 2 | 12 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0003 | 0/0 | 2817 | 37 | 18 | 1 | 15 | 0 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0004 | 0/0 | 2817 | 5 | 4 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0005 | 0/0 | 2817 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0006 | 0/0 | 2817 | 4 | 1 | 0 | 1 | 1 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0008 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0010 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0012 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0013 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0001c0015 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0002c0007 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0003c0009 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 | ||
| a0004c0014 | 0/0 | 2842 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2837): Show |
chr11 | 920870 | 1017240 | ||
| a0005c0011 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | ATGCC others(2812): Show |
chr11 | 920870 | 1017240 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4587 | 93 | 19 | 19 | 42 | 6 | 7 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0002 | 0/0 | 4587 | 2 | 0 | 1 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0003 | 0/0 | 4587 | 3 | 0 | 0 | 1 | 0 | 2 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0005 | 0/0 | 4587 | 8 | 1 | 6 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0006 | 0/0 | 4587 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0007 | 0/0 | 4587 | 6 | 0 | 2 | 0 | 3 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0013 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0014 | 0/0 | 4587 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0015 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0016 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0017 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0001t0019 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0001 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0002 | 1/1 | 4587 | 41 | 9 | 11 | 15 | 1 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0003 | 0/0 | 4587 | 29 | 0 | 4 | 16 | 0 | 9 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0004 | 0/0 | 4587 | 13 | 11 | 2 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0005 | 0/0 | 4587 | 3 | 3 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0011 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0002t0012 | 0/0 | 4587 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0003t0002 | 0/0 | 4587 | 28 | 12 | 0 | 13 | 0 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0003t0004 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0003t0006 | 0/0 | 4587 | 6 | 6 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0003t0008 | 0/0 | 4587 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0004t0002 | 0/0 | 4587 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0004t0009 | 0/0 | 4587 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0004t0010 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0005t0003 | 0/0 | 4587 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0006t0001 | 0/0 | 4587 | 3 | 0 | 0 | 1 | 1 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0006t0018 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0008t0004 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0010t0005 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0012t0001 | 0/0 | 4587 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0013t0001 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0001c0015t0003 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0002c0007t0004 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0003c0009t0003 | 0/0 | 4587 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| a0004c0014t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4607): Show |
chr11 | 920870 | 1017240 |
| a0005c0011t0002 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | AGAAA others(4582): Show |
chr11 | 920870 | 1017240 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0014g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0016g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0001t0019g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0002t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0003t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0004t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0004t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0004t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0004t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0005t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0005t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0005t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0005t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0006t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0008t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0010t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0012t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0013t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0001c0015t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0002c0007t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0003c0009t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0004c0014t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| a0005c0011t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0091 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0106 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0221 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0137 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00609 | hp1 | a0001 | c0015 | t0003 | g0174 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00621 | hp1 | a0001 | c0005 | t0003 | g0144 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00673 | hp2 | a0001 | c0006 | t0001 | g0044 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00738 | hp1 | a0001 | c0001 | t0019 | g0021 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0152 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0040 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0175 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01109 | hp1 | a0001 | c0013 | t0001 | g0128 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0222 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01243 | hp1 | a0001 | c0008 | t0004 | g0236 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01243 | hp2 | a0001 | c0004 | t0009 | g0259 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0141 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0223 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0090 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0172 | EUR | IBS | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0227 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0155 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01943 | hp1 | a0001 | c0003 | t0004 | g0255 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01981 | hp1 | a0001 | c0001 | t0016 | g0046 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0167 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0145 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02056 | hp2 | a0001 | c0003 | t0008 | g0189 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0199 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02135 | hp2 | a0001 | c0003 | t0008 | g0193 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | CDX | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02257 | hp1 | a0001 | c0004 | t0010 | g0169 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0194 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0217 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02280 | hp2 | a0001 | c0003 | t0006 | g0265 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0235 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0204 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0210 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0135 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0231 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02615 | hp2 | a0001 | c0006 | t0018 | g0100 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02622 | hp1 | a0002 | c0007 | t0004 | g0224 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02630 | hp1 | a0001 | c0003 | t0006 | g0138 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0230 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0179 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02698 | hp1 | a0003 | c0009 | t0003 | g0154 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0153 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0228 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0203 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0006 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0254 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0212 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0218 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0252 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0180 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0263 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0149 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0253 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03654 | hp1 | a0001 | c0006 | t0001 | g0037 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0089 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03704 | hp1 | a0001 | c0005 | t0003 | g0132 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0084 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0258 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0143 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0190 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0003 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0142 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0237 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0183 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04199 | hp1 | a0001 | c0012 | t0001 | g0097 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0151 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0159 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0126 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0161 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18522 | hp2 | a0001 | c0010 | t0005 | g0148 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | CHB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18747 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | CHB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18939 | hp2 | a0001 | c0002 | t0011 | g0168 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0207 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18994 | hp1 | a0004 | c0014 | t0001 | g0261 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19004 | hp2 | a0001 | c0005 | t0003 | g0192 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19005 | hp1 | a0001 | c0005 | t0003 | g0181 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0064 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0198 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0264 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0170 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19082 | hp1 | a0005 | c0011 | t0002 | g0242 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0069 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19240 | hp1 | a0001 | c0004 | t0009 | g0260 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0195 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | ASW | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0267 | AFR | ASW | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20752 | hp1 | a0001 | c0006 | t0001 | g0127 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20805 | hp1 | a0001 | c0002 | t0012 | g0001 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0092 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | GIH | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0229 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0216 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0196 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0162 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0146 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| NA20300 | hp2 | a0001 | c0003 | t0006 | g0266 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0220 | REF | REF | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0157 | REF | REF | AP2A2_chr11_920870_1017240 | AP2A2 | chr11 | 920870 | 1017240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:985555 | C | T | 1 | a0005 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.935C>T | p.Ala312Val | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/22 | 1087/4587 | 935/2820 | 312/939 | chr11 | 985555 | |||
| chr11:993808 | C | CACCCGCG others(18): Show |
1 | a0004 | 1 | NA18994.hp1 | frameshift_variant | HIGH | c.1608_1632dupCCGCGC others(19): Show |
p.Ile545fs | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1785/4587 | 1633/2820 | 545/939 | INFO_REALIGN_3_PRIME | chr11 | 993808 | ||
| chr11:993809 | A | C | 1 | a0003 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1606A>C | p.Thr536Pro | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1758/4587 | 1606/2820 | 536/939 | chr11 | 993809 | |||
| chr11:993891 | G | A | 1 | a0002 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1688G>A | p.Arg563His | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1840/4587 | 1688/2820 | 563/939 | chr11 | 993891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:972118 | C | A | 1 | a0001c0005 | 4 | HG00621.hp1 HG03704.hp1 NA19004.hp2 others(1): Show |
synonymous_variant | LOW | c.336C>A | p.Ile112Ile | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/22 | 488/4587 | 336/2820 | 112/939 | chr11 | 972118 | |||
| chr11:981236 | A | G | 1 | a0001c0015 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.642A>G | p.Leu214Leu | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/22 | 794/4587 | 642/2820 | 214/939 | chr11 | 981236 | |||
| chr11:985547 | C | T | 5 | a0001c0001 a0001c0006 a0001c0012 others(2): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
synonymous_variant | LOW | c.927C>T | p.Leu309Leu | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/22 | 1079/4587 | 927/2820 | 309/939 | chr11 | 985547 | |||
| chr11:988638 | C | T | 1 | a0001c0010 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1218C>T | p.Ala406Ala | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/22 | 1370/4587 | 1218/2820 | 406/939 | chr11 | 988638 | |||
| chr11:993817 | G | A | 2 | a0001c0012 a0001c0013 |
2 | HG01109.hp1 HG04199.hp1 |
synonymous_variant | LOW | c.1614G>A | p.Ala538Ala | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1766/4587 | 1614/2820 | 538/939 | chr11 | 993817 | |||
| chr11:993907 | C | G | 4 | a0001c0003 a0001c0006 a0001c0013 others(1): Show |
43 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(40): Show |
synonymous_variant | LOW | c.1704C>G | p.Leu568Leu | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1856/4587 | 1704/2820 | 568/939 | chr11 | 993907 | |||
| chr11:993964 | C | T | 1 | a0001c0004 | 5 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.1761C>T | p.Thr587Thr | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/22 | 1913/4587 | 1761/2820 | 587/939 | chr11 | 993964 | |||
| chr11:994134 | C | G | 1 | a0002c0007 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1845C>G | p.Leu615Leu | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/22 | 1997/4587 | 1845/2820 | 615/939 | chr11 | 994134 | |||
| chr11:994209 | G | T | 1 | a0001c0008 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1920G>T | p.Gly640Gly | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/22 | 2072/4587 | 1920/2820 | 640/939 | chr11 | 994209 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:925940 | C | A | 1 | a0001c0004t0010 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/22 | 82 | chr11 | 925940 | ||||||
| chr11:925949 | C | A | 1 | a0001c0003t0008 | 2 | HG02056.hp2 HG02135.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/22 | 73 | chr11 | 925949 | ||||||
| chr11:925967 | C | T | 1 | a0001c0001t0019 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/22 | 55 | chr11 | 925967 | ||||||
| chr11:925970 | C | T | 1 | a0001c0006t0018 | 1 | HG02615.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/22 | chr11 | 925970 | |||||||
| chr11:1010649 | C | T | 6 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0008 others(3): Show |
40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 24 | chr11 | 1010649 | ||||||
| chr11:1010650 | G | A | 1 | a0001c0004t0009 | 2 | HG01243.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*25G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 25 | chr11 | 1010650 | ||||||
| chr11:1010694 | C | T | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(13): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*69C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 69 | chr11 | 1010694 | ||||||
| chr11:1010750 | G | A | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(10): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*125G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 125 | chr11 | 1010750 | ||||||
| chr11:1010876 | C | T | 3 | a0001c0001t0005 a0001c0002t0005 a0001c0010t0005 |
12 | HG01106.hp2 HG01258.hp1 HG01261.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*251C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 251 | chr11 | 1010876 | ||||||
| chr11:1010917 | T | C | 4 | a0001c0002t0004 a0001c0003t0004 a0001c0008t0004 others(1): Show |
16 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*292T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 292 | chr11 | 1010917 | ||||||
| chr11:1010946 | G | A | 1 | a0001c0001t0013 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 321 | chr11 | 1010946 | ||||||
| chr11:1011490 | G | A | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(13): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*865G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 865 | chr11 | 1011490 | ||||||
| chr11:1011597 | G | A | 2 | a0001c0001t0007 a0001c0001t0019 |
7 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*972G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 972 | chr11 | 1011597 | ||||||
| chr11:1011657 | G | A | 1 | a0001c0002t0011 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1032G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1032 | chr11 | 1011657 | ||||||
| chr11:1011745 | T | C | 1 | a0001c0002t0012 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1120T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1120 | chr11 | 1011745 | ||||||
| chr11:1011829 | T | C | 15 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(12): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1204T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1204 | chr11 | 1011829 | ||||||
| chr11:1011886 | G | A | 1 | a0001c0001t0014 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1261 | chr11 | 1011886 | ||||||
| chr11:1011985 | C | T | 1 | a0001c0001t0016 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1360C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1360 | chr11 | 1011985 | ||||||
| chr11:1012102 | G | A | 1 | a0001c0001t0015 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 22/22 | 1477 | chr11 | 1012102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:926103 | C | A | 2 | a0001c0002t0003g0002 a0001c0002t0003g0003 |
2 | HG03927.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.67+15C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926103 | |||||||
| chr11:926295 | C | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+207C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926295 | |||||||
| chr11:926671 | T | C | 1 | a0001c0003t0002g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.67+583T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926671 | |||||||
| chr11:926743 | C | T | 5 | a0001c0003t0006g0263 a0001c0003t0006g0264 a0001c0003t0006g0265 others(2): Show |
5 | HG02280.hp2 HG03516.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+655C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926743 | |||||||
| chr11:926809 | G | A | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+721G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926809 | |||||||
| chr11:926870 | G | T | 127 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+782G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926870 | |||||||
| chr11:926950 | C | T | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+862C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926950 | |||||||
| chr11:926958 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+870C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 926958 | |||||||
| chr11:927020 | C | T | 130 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.67+932C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927020 | |||||||
| chr11:927077 | T | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+989T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927077 | |||||||
| chr11:927099 | C | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67+1011C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927099 | |||||||
| chr11:927108 | T | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.67+1020T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927108 | |||||||
| chr11:927160 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.67+1072G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927160 | |||||||
| chr11:927250 | TG | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(162): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.67+1169delG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927250 | ||||||
| chr11:927257 | G | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0116 others(5): Show |
8 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+1169G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927257 | |||||||
| chr11:927261 | C | A | 1 | a0001c0005t0003g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+1173C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927261 | |||||||
| chr11:927344 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+1256C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927344 | |||||||
| chr11:927355 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+1267G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927355 | |||||||
| chr11:927419 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67+1331C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927419 | |||||||
| chr11:927500 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+1412T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927500 | |||||||
| chr11:927508 | G | GT | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1422dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927508 | ||||||
| chr11:927510 | TA | T | 28 | a0001c0001t0001g0115 a0001c0002t0002g0208 a0001c0002t0002g0213 others(25): Show |
28 | HG00544.hp2 HG02083.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+1439delA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927510 | ||||||
| chr11:927553 | A | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+1465A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927553 | |||||||
| chr11:927614 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.67+1526G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927614 | |||||||
| chr11:927652 | C | A | 1 | a0001c0002t0004g0222 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.67+1564C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927652 | |||||||
| chr11:927816 | C | CA | 159 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.67+1752dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927816 | ||||||
| chr11:927816 | C | CAA | 34 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00738.hp1 HG01106.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.67+1751_67+1752dup others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927816 | ||||||
| chr11:927913 | C | G | 1 | a0001c0003t0002g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.67+1825C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927913 | |||||||
| chr11:927993 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1905C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 927993 | |||||||
| chr11:928382 | G | A | 1 | a0001c0010t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+2294G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928382 | |||||||
| chr11:928402 | C | T | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.67+2314C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928402 | |||||||
| chr11:928594 | C | T | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+2506C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928594 | |||||||
| chr11:928598 | T | A | 129 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.67+2510T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928598 | |||||||
| chr11:928669 | C | A | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.67+2581C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928669 | |||||||
| chr11:928702 | C | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+2614C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928702 | |||||||
| chr11:928758 | G | C | 1 | a0001c0005t0003g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+2670G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928758 | |||||||
| chr11:928790 | C | T | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+2702C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928790 | |||||||
| chr11:928843 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+2755C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928843 | |||||||
| chr11:928856 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+2768C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928856 | |||||||
| chr11:928886 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+2798C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 928886 | |||||||
| chr11:929055 | A | G | 1 | a0001c0008t0004g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.67+2967A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929055 | |||||||
| chr11:929111 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+3023C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929111 | |||||||
| chr11:929220 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | NA18950.hp1 NA18983.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+3132G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929220 | |||||||
| chr11:929220 | G | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67+3132G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929220 | |||||||
| chr11:929269 | A | G | 129 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.67+3181A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929269 | |||||||
| chr11:929269 | A | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+3181A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929269 | |||||||
| chr11:929342 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
12 | HG02056.hp1 HG02132.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+3254C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929342 | |||||||
| chr11:929374 | A | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+3286A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929374 | |||||||
| chr11:929476 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+3388C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929476 | |||||||
| chr11:929521 | A | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+3433A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929521 | |||||||
| chr11:929632 | A | G | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+3544A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929632 | |||||||
| chr11:929680 | C | T | 1 | a0001c0004t0009g0259 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67+3592C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929680 | |||||||
| chr11:929745 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+3657C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929745 | |||||||
| chr11:929932 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.67+3844G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 929932 | |||||||
| chr11:930027 | G | A | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+3939G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930027 | |||||||
| chr11:930120 | C | CA | 32 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(29): Show |
32 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.67+4055dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 930120 | ||||||
| chr11:930120 | CA | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+4055delA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 930120 | ||||||
| chr11:930120 | CAAA | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+4053_67+4055del others(3): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 930120 | ||||||
| chr11:930692 | T | C | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+4604T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930692 | |||||||
| chr11:930715 | T | A | 1 | a0001c0001t0001g0017 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.67+4627T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930715 | |||||||
| chr11:930741 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0024 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.67+4653C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930741 | |||||||
| chr11:930771 | C | T | 32 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0141 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+4683C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930771 | |||||||
| chr11:930772 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+4684G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930772 | |||||||
| chr11:930939 | G | T | 1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+4851G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 930939 | |||||||
| chr11:931550 | A | C | 1 | a0001c0002t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.67+5462A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 931550 | |||||||
| chr11:931568 | C | T | 1 | a0001c0002t0004g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+5480C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 931568 | |||||||
| chr11:931642 | G | A | 1 | a0001c0002t0003g0002 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.67+5554G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 931642 | |||||||
| chr11:931648 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+5560G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 931648 | |||||||
| chr11:931802 | G | GT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(26): Show |
29 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+5733dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 931802 | ||||||
| chr11:931802 | GT | G | 9 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+5733delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 931802 | ||||||
| chr11:931802 | GTT | G | 22 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0225 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+5732_67+5733del others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 931802 | ||||||
| chr11:931959 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(6): Show |
9 | HG01081.hp1 HG01346.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+5871C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 931959 | |||||||
| chr11:932066 | A | T | 1 | a0001c0012t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+5978A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932066 | |||||||
| chr11:932079 | A | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+5991A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932079 | |||||||
| chr11:932167 | G | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+6079G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932167 | |||||||
| chr11:932204 | C | T | 1 | a0001c0002t0003g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.67+6116C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932204 | |||||||
| chr11:932212 | C | T | 2 | a0001c0002t0002g0139 a0001c0002t0002g0140 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.67+6124C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932212 | |||||||
| chr11:932304 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+6216G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932304 | |||||||
| chr11:932444 | G | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+6356G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932444 | |||||||
| chr11:932449 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67+6361C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932449 | |||||||
| chr11:932501 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | NA18950.hp1 NA18983.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+6413A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932501 | |||||||
| chr11:932664 | A | G | 1 | a0001c0003t0002g0215 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.67+6576A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932664 | |||||||
| chr11:932710 | G | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+6622G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932710 | |||||||
| chr11:932846 | T | TA | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+6759dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 932846 | ||||||
| chr11:932898 | T | C | 31 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(28): Show |
31 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.67+6810T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932898 | |||||||
| chr11:932988 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+6900C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 932988 | |||||||
| chr11:933008 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.67+6920G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933008 | |||||||
| chr11:933028 | G | T | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+6940G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933028 | |||||||
| chr11:933138 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.67+7050C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933138 | |||||||
| chr11:933145 | G | A | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+7057G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933145 | |||||||
| chr11:933209 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0094 |
2 | HG00140.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.67+7121A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933209 | |||||||
| chr11:933224 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+7136C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933224 | |||||||
| chr11:933269 | AAAAC | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+7193_67+7196del others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 933269 | ||||||
| chr11:933360 | T | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+7272T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933360 | |||||||
| chr11:933462 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67+7374A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933462 | |||||||
| chr11:933498 | TC | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+7413delC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 933498 | ||||||
| chr11:933579 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+7491C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933579 | |||||||
| chr11:933588 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.67+7500G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933588 | |||||||
| chr11:933631 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+7543C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933631 | |||||||
| chr11:933783 | A | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+7695A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933783 | |||||||
| chr11:933813 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+7725C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933813 | |||||||
| chr11:933865 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+7777T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933865 | |||||||
| chr11:933873 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+7785C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933873 | |||||||
| chr11:933919 | C | T | 1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.67+7831C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 933919 | |||||||
| chr11:934094 | C | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+8006C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934094 | |||||||
| chr11:934104 | G | A | 140 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.67+8016G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934104 | |||||||
| chr11:934434 | C | G | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8346C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934434 | |||||||
| chr11:934594 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+8506C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934594 | |||||||
| chr11:934750 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+8662G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934750 | |||||||
| chr11:934807 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+8719G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934807 | |||||||
| chr11:934863 | C | CT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8787dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 934863 | ||||||
| chr11:934924 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+8836T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 934924 | |||||||
| chr11:935002 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.67+8914G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935002 | |||||||
| chr11:935059 | A | ATT | 130 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.67+8983_67+8984dup others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935059 | ||||||
| chr11:935059 | A | ATTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | NA18950.hp1 NA18964.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8982_67+8984dup others(3): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935059 | ||||||
| chr11:935059 | AT | A | 7 | a0001c0003t0002g0200 a0001c0003t0006g0138 a0001c0003t0006g0263 others(4): Show |
7 | HG02083.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+8984delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935059 | ||||||
| chr11:935142 | C | T | 2 | a0001c0001t0001g0114 a0001c0005t0003g0132 |
2 | HG03704.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.67+9054C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935142 | |||||||
| chr11:935195 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+9107A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935195 | |||||||
| chr11:935209 | C | T | 1 | a0001c0003t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.67+9121C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935209 | |||||||
| chr11:935216 | C | T | 1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.67+9128C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935216 | |||||||
| chr11:935248 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+9160G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935248 | |||||||
| chr11:935274 | G | A | 1 | a0001c0002t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67+9186G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935274 | |||||||
| chr11:935295 | G | A | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+9207G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935295 | |||||||
| chr11:935343 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+9255C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935343 | |||||||
| chr11:935390 | A | C | 1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.67+9302A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935390 | |||||||
| chr11:935419 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+9331C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935419 | |||||||
| chr11:935491 | A | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.67+9403A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935491 | |||||||
| chr11:935546 | C | G | 1 | a0001c0002t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.67+9458C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935546 | |||||||
| chr11:935578 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+9490A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935578 | |||||||
| chr11:935597 | C | T | 1 | a0001c0002t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.67+9509C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935597 | |||||||
| chr11:935603 | G | GTTTTT | 6 | a0001c0002t0002g0133 a0001c0002t0002g0159 a0001c0002t0002g0160 others(3): Show |
6 | HG00609.hp1 HG01516.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+9533_67+9537dup others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(5): Show |
1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+9523_67+9524ins others(12): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(3): Show |
2 | a0001c0002t0002g0004 a0001c0004t0009g0260 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67+9528_67+9537dup others(10): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(4): Show |
12 | a0001c0002t0002g0139 a0001c0002t0002g0140 a0001c0002t0003g0201 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+9527_67+9537dup others(11): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(5): Show |
14 | a0001c0002t0002g0001 a0001c0002t0002g0208 a0001c0002t0003g0206 others(11): Show |
14 | HG02027.hp1 HG02523.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+9526_67+9537dup others(12): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(6): Show |
6 | a0001c0002t0002g0213 a0001c0002t0002g0246 a0001c0003t0002g0134 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+9525_67+9537dup others(13): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(7): Show |
2 | a0001c0003t0002g0199 a0001c0003t0002g0214 |
2 | HG02135.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.67+9524_67+9537dup others(14): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(8): Show |
1 | a0001c0003t0006g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67+9523_67+9537dup others(15): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(9): Show |
1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+9522_67+9537dup others(16): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(10): Show |
14 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0151 others(11): Show |
14 | HG00558.hp1 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+9521_67+9537dup others(17): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(11): Show |
12 | a0001c0002t0003g0003 a0001c0002t0003g0143 a0001c0002t0003g0153 others(9): Show |
12 | HG01081.hp1 HG02040.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+9520_67+9537dup others(18): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(12): Show |
1 | a0001c0002t0003g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.67+9519_67+9537dup others(19): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(13): Show |
1 | a0001c0002t0003g0002 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.67+9518_67+9537dup others(20): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(14): Show |
1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+9517_67+9537dup others(21): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(15): Show |
2 | a0001c0003t0006g0265 a0001c0003t0008g0189 |
2 | HG02056.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.67+9516_67+9537dup others(22): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(16): Show |
4 | a0001c0002t0002g0239 a0001c0002t0002g0247 a0001c0003t0008g0193 others(1): Show |
4 | HG02135.hp2 NA18964.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(23): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(17): Show |
5 | a0001c0002t0002g0240 a0001c0002t0002g0243 a0001c0002t0002g0245 others(2): Show |
5 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(24): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(18): Show |
2 | a0001c0002t0002g0248 a0001c0005t0003g0144 |
2 | HG00621.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(25): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(19): Show |
1 | a0001c0002t0002g0241 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.67+9537_67+9538ins others(26): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(21): Show |
2 | a0001c0002t0002g0257 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(28): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(22): Show |
5 | a0001c0001t0001g0123 a0001c0002t0002g0249 a0001c0003t0006g0266 others(2): Show |
5 | HG02040.hp2 HG03942.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(29): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(23): Show |
4 | a0001c0002t0002g0171 a0001c0002t0002g0244 a0001c0002t0002g0251 others(1): Show |
4 | HG01081.hp2 HG03516.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(30): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(24): Show |
4 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0002t0002g0165 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(31): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(25): Show |
2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | HG01943.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(32): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | G | GTTTTTTT others(26): Show |
2 | a0001c0001t0003g0130 a0001c0002t0011g0168 |
2 | NA18939.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.67+9537_67+9538ins others(33): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | GTT | G | 21 | a0001c0001t0001g0022 a0001c0001t0001g0122 a0001c0001t0006g0010 others(18): Show |
21 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+9536_67+9537del others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | GTTT | G | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.67+9535_67+9537del others(3): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935603 | GTTTTTT | G | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+9532_67+9537del others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935603 | ||||||
| chr11:935794 | C | T | 7 | a0001c0001t0007g0040 a0001c0001t0007g0089 a0001c0001t0007g0090 others(4): Show |
7 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+9706C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935794 | |||||||
| chr11:935823 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.67+9735C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935823 | |||||||
| chr11:935900 | CT | C | 5 | a0001c0001t0001g0039 a0001c0001t0003g0130 a0001c0002t0002g0004 others(2): Show |
5 | HG02055.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+9827delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 935900 | ||||||
| chr11:935967 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+9879T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935967 | |||||||
| chr11:936058 | C | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+9970C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936058 | |||||||
| chr11:936068 | A | AT | 7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0129 others(4): Show |
7 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+9994dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 936068 | ||||||
| chr11:936076 | T | A | 1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.67+9988T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936076 | |||||||
| chr11:936077 | T | A | 4 | a0001c0002t0003g0182 a0001c0003t0002g0135 a0001c0003t0002g0161 others(1): Show |
4 | HG02572.hp2 HG03471.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+9989T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936077 | |||||||
| chr11:936078 | T | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+9990T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936078 | |||||||
| chr11:936082 | T | C | 1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.67+9994T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936082 | |||||||
| chr11:936097 | T | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.67+10009T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936097 | |||||||
| chr11:936098 | G | A | 1 | a0001c0002t0004g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+10010G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936098 | |||||||
| chr11:936098 | G | C | 1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.67+10010G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936098 | |||||||
| chr11:936198 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+10110C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936198 | |||||||
| chr11:936206 | C | CT | 47 | a0001c0001t0001g0022 a0001c0001t0001g0123 a0001c0001t0002g0099 others(44): Show |
47 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+10141dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 936206 | ||||||
| chr11:936206 | C | CTTT | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0129 others(5): Show |
8 | HG01109.hp1 HG02129.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10139_67+10141d others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 936206 | ||||||
| chr11:936206 | CT | C | 19 | a0001c0001t0001g0093 a0001c0001t0006g0009 a0001c0001t0006g0010 others(16): Show |
19 | HG01069.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.67+10141delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 936206 | ||||||
| chr11:936251 | C | T | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+10163C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936251 | |||||||
| chr11:936412 | T | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+10324T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936412 | |||||||
| chr11:936711 | G | A | 32 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0141 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+10623G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 936711 | |||||||
| chr11:937133 | C | T | 1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+11045C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937133 | |||||||
| chr11:937176 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+11088T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937176 | |||||||
| chr11:937186 | A | G | 1 | a0001c0003t0002g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67+11098A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937186 | |||||||
| chr11:937304 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.67+11216G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937304 | |||||||
| chr11:937346 | G | A | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+11258G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937346 | |||||||
| chr11:937478 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+11390C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937478 | |||||||
| chr11:937569 | T | C | 1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+11481T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937569 | |||||||
| chr11:937626 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+11538C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937626 | |||||||
| chr11:937697 | AATTT | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+11613_67+11616d others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 937697 | ||||||
| chr11:937740 | G | A | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+11652G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937740 | |||||||
| chr11:937804 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11716G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937804 | |||||||
| chr11:937953 | G | A | 1 | a0001c0002t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67+11865G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937953 | |||||||
| chr11:937998 | A | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11910A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 937998 | |||||||
| chr11:938055 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+11967C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938055 | |||||||
| chr11:938366 | G | A | 2 | a0001c0002t0002g0160 a0001c0002t0004g0170 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+12278G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938366 | |||||||
| chr11:938449 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+12361C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938449 | |||||||
| chr11:938477 | G | GT | 13 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+12404dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 938477 | ||||||
| chr11:938593 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+12505G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938593 | |||||||
| chr11:938675 | C | T | 1 | a0001c0001t0005g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.67+12587C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938675 | |||||||
| chr11:938808 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+12720G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938808 | |||||||
| chr11:938892 | T | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.67+12804T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938892 | |||||||
| chr11:938975 | C | G | 2 | a0001c0002t0002g0160 a0001c0002t0004g0170 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+12887C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 938975 | |||||||
| chr11:939231 | C | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
12 | HG02056.hp1 HG02132.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+13143C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939231 | |||||||
| chr11:939247 | C | CA | 10 | a0001c0001t0001g0042 a0001c0001t0001g0108 a0001c0001t0001g0117 others(7): Show |
10 | HG01192.hp1 HG01243.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+13178dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 939247 | ||||||
| chr11:939247 | C | CAAA | 15 | a0001c0002t0002g0225 a0001c0002t0002g0256 a0001c0002t0004g0222 others(12): Show |
15 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+13176_67+13178d others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 939247 | ||||||
| chr11:939280 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.67+13192A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939280 | |||||||
| chr11:939382 | G | C | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+13294G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939382 | |||||||
| chr11:939451 | T | C | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+13363T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939451 | |||||||
| chr11:939471 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+13383G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939471 | |||||||
| chr11:939476 | G | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+13388G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939476 | |||||||
| chr11:939490 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+13402G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939490 | |||||||
| chr11:939498 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+13410A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939498 | |||||||
| chr11:939500 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+13412A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939500 | |||||||
| chr11:939586 | A | G | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+13498A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939586 | |||||||
| chr11:939594 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+13506G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939594 | |||||||
| chr11:939693 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.67+13605C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939693 | |||||||
| chr11:939696 | C | T | 29 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(26): Show |
29 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+13608C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939696 | |||||||
| chr11:939793 | A | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.67+13705A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939793 | |||||||
| chr11:939863 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+13775G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939863 | |||||||
| chr11:939897 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+13809T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939897 | |||||||
| chr11:939941 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+13853G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939941 | |||||||
| chr11:939951 | C | CT | 32 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(29): Show |
32 | HG00621.hp1 HG00621.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+13885dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 939951 | ||||||
| chr11:939951 | CTTTT | C | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.67+13882_67+13885d others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 939951 | ||||||
| chr11:939987 | A | T | 1 | a0001c0001t0005g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.67+13899A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 939987 | |||||||
| chr11:940047 | C | T | 1 | a0001c0005t0003g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67+13959C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940047 | |||||||
| chr11:940248 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+14160C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940248 | |||||||
| chr11:940280 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+14192C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940280 | |||||||
| chr11:940472 | TTC | T | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+14386_67+14387d others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 940472 | ||||||
| chr11:940612 | T | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14524T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940612 | |||||||
| chr11:940624 | TG | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+14537delG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940624 | |||||||
| chr11:940631 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0094 |
2 | HG00140.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.67+14543G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940631 | |||||||
| chr11:940654 | T | G | 1 | a0001c0003t0002g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.67+14566T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940654 | |||||||
| chr11:940958 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0105 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.67+14870G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940958 | |||||||
| chr11:940991 | A | G | 31 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(28): Show |
31 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.67+14903A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 940991 | |||||||
| chr11:941145 | C | G | 1 | a0001c0002t0004g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+15057C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941145 | |||||||
| chr11:941154 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0105 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.67+15066G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941154 | |||||||
| chr11:941208 | G | A | 1 | a0001c0003t0002g0134 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.67+15120G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941208 | |||||||
| chr11:941300 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+15212G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941300 | |||||||
| chr11:941391 | T | C | 1 | a0001c0002t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67+15303T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941391 | |||||||
| chr11:941497 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67+15409G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941497 | |||||||
| chr11:941625 | T | C | 1 | a0001c0002t0002g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.67+15537T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941625 | |||||||
| chr11:941656 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.67+15568C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941656 | |||||||
| chr11:941687 | A | G | 1 | a0001c0002t0003g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.67+15599A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941687 | |||||||
| chr11:941844 | C | T | 6 | a0001c0001t0003g0103 a0001c0001t0005g0082 a0001c0001t0005g0083 others(3): Show |
6 | HG01258.hp1 HG01261.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+15756C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941844 | |||||||
| chr11:941848 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+15760A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941848 | |||||||
| chr11:941907 | G | GT | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+15820dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 941907 | ||||||
| chr11:941933 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+15845C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941933 | |||||||
| chr11:941939 | A | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+15851A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941939 | |||||||
| chr11:941941 | A | T | 158 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.67+15853A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941941 | |||||||
| chr11:941966 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+15878A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 941966 | |||||||
| chr11:942088 | G | A | 27 | a0001c0001t0007g0106 a0001c0002t0002g0001 a0001c0002t0002g0139 others(24): Show |
27 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.67+16000G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942088 | |||||||
| chr11:942344 | G | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.67+16256G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942344 | |||||||
| chr11:942690 | A | G | 1 | a0001c0001t0005g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.67+16602A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942690 | |||||||
| chr11:942701 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+16613T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942701 | |||||||
| chr11:942818 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68-16619C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942818 | |||||||
| chr11:942941 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.68-16496T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 942941 | |||||||
| chr11:943002 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-16435C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943002 | |||||||
| chr11:943003 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.68-16434G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943003 | |||||||
| chr11:943106 | A | G | 1 | a0001c0002t0004g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.68-16331A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943106 | |||||||
| chr11:943228 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-16209C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943228 | |||||||
| chr11:943231 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-16206A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943231 | |||||||
| chr11:943341 | T | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-16096T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943341 | |||||||
| chr11:943473 | G | A | 2 | a0001c0001t0003g0103 a0001c0001t0005g0082 |
2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.68-15964G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943473 | |||||||
| chr11:943518 | T | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.68-15919T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943518 | |||||||
| chr11:943521 | T | G | 1 | a0001c0001t0005g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.68-15916T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943521 | |||||||
| chr11:943545 | G | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.68-15892G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943545 | |||||||
| chr11:943611 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-15826G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943611 | |||||||
| chr11:943695 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-15742G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943695 | |||||||
| chr11:943827 | A | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-15610A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943827 | |||||||
| chr11:943831 | T | C | 1 | a0001c0001t0005g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-15606T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943831 | |||||||
| chr11:943837 | C | T | 1 | a0001c0002t0003g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.68-15600C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943837 | |||||||
| chr11:943865 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-15572A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943865 | |||||||
| chr11:943917 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-15520G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943917 | |||||||
| chr11:943940 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-15497G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 943940 | |||||||
| chr11:944141 | C | T | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-15296C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944141 | |||||||
| chr11:944190 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.68-15247C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944190 | |||||||
| chr11:944226 | A | G | 1 | a0001c0002t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.68-15211A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944226 | |||||||
| chr11:944466 | A | G | 230 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.68-14971A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944466 | |||||||
| chr11:944479 | T | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-14958T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944479 | |||||||
| chr11:944583 | A | G | 1 | a0001c0003t0002g0197 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.68-14854A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944583 | |||||||
| chr11:944608 | G | A | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-14829G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944608 | |||||||
| chr11:944727 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-14710C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944727 | |||||||
| chr11:944734 | A | C | 1 | a0001c0002t0002g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-14703A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944734 | |||||||
| chr11:944801 | C | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.68-14636C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944801 | |||||||
| chr11:944809 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-14628C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944809 | |||||||
| chr11:944810 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-14627G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944810 | |||||||
| chr11:944871 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-14566G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 944871 | |||||||
| chr11:945576 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-13861G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 945576 | |||||||
| chr11:945678 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.68-13759T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 945678 | |||||||
| chr11:945912 | C | T | 3 | a0001c0001t0006g0009 a0001c0001t0006g0010 a0001c0003t0002g0210 |
3 | HG02523.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68-13525C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 945912 | |||||||
| chr11:946070 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-13367A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946070 | |||||||
| chr11:946228 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-13209C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946228 | |||||||
| chr11:946294 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-13143T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946294 | |||||||
| chr11:946360 | G | A | 1 | a0002c0007t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-13077G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946360 | |||||||
| chr11:946386 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-13051C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946386 | |||||||
| chr11:946484 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-12953G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946484 | |||||||
| chr11:946495 | G | A | 1 | a0001c0002t0003g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-12942G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946495 | |||||||
| chr11:946577 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.68-12860T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946577 | |||||||
| chr11:946643 | C | T | 1 | a0001c0003t0002g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.68-12794C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946643 | |||||||
| chr11:946770 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0047 a0001c0002t0004g0235 a0001c0002t0004g0254 |
3 | HG02451.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.68-12658_68-12657i others(17): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 946770 | ||||||
| chr11:946770 | C | CAAAAAAA others(9): Show |
21 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0001g0087 others(18): Show |
21 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.68-12658_68-12657i others(18): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 946770 | ||||||
| chr11:946770 | C | CAAAAAAA others(10): Show |
97 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.68-12658_68-12657i others(19): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 946770 | ||||||
| chr11:946770 | C | CAAAAAAA others(11): Show |
14 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0049 others(11): Show |
14 | HG00642.hp1 HG00642.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-12658_68-12657i others(20): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 946770 | ||||||
| chr11:946770 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0108 a0001c0001t0016g0046 |
3 | HG01981.hp1 HG02056.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.68-12658_68-12657i others(21): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 946770 | ||||||
| chr11:946780 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.68-12657G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946780 | |||||||
| chr11:946985 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-12452T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 946985 | |||||||
| chr11:947010 | C | CT | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.68-12410dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 947010 | ||||||
| chr11:947010 | CT | C | 124 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(121): Show |
124 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.68-12410delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 947010 | ||||||
| chr11:947048 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-12389C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947048 | |||||||
| chr11:947065 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-12372G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947065 | |||||||
| chr11:947302 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68-12135C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947302 | |||||||
| chr11:947451 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-11986C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947451 | |||||||
| chr11:947452 | G | A | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68-11985G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947452 | |||||||
| chr11:947538 | C | G | 157 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.68-11899C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947538 | |||||||
| chr11:947585 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.68-11852T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947585 | |||||||
| chr11:947651 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-11786T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947651 | |||||||
| chr11:947656 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-11781C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947656 | |||||||
| chr11:947664 | C | T | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.68-11773C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947664 | |||||||
| chr11:947781 | G | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68-11656G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 947781 | |||||||
| chr11:947799 | CA | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-11629delA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 947799 | ||||||
| chr11:948119 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.68-11318A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948119 | |||||||
| chr11:948121 | G | A | 1 | a0001c0002t0003g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-11316G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948121 | |||||||
| chr11:948299 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-11138G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948299 | |||||||
| chr11:948301 | T | C | 1 | a0001c0002t0002g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-11136T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948301 | |||||||
| chr11:948347 | C | T | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.68-11090C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948347 | |||||||
| chr11:948379 | G | A | 2 | a0001c0001t0014g0126 a0001c0002t0004g0230 |
2 | HG02630.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.68-11058G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948379 | |||||||
| chr11:948384 | C | G | 1 | a0001c0001t0005g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-11053C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948384 | |||||||
| chr11:948424 | C | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-11013C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948424 | |||||||
| chr11:948677 | G | A | 2 | a0001c0006t0001g0127 a0001c0013t0001g0128 |
2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.68-10760G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948677 | |||||||
| chr11:948695 | C | T | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.68-10742C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948695 | |||||||
| chr11:948704 | A | G | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.68-10733A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948704 | |||||||
| chr11:948712 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-10725T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948712 | |||||||
| chr11:948731 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-10706G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948731 | |||||||
| chr11:948740 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-10697A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948740 | |||||||
| chr11:948848 | C | CAA | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-10589_68-10588i others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948848 | |||||||
| chr11:948887 | A | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-10550A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 948887 | |||||||
| chr11:949030 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-10407C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949030 | |||||||
| chr11:949121 | C | T | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-10316C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949121 | |||||||
| chr11:949129 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-10308G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949129 | |||||||
| chr11:949146 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.68-10291C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949146 | |||||||
| chr11:949354 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-10083G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949354 | |||||||
| chr11:949601 | C | A | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-9836C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949601 | |||||||
| chr11:949647 | T | C | 150 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.68-9790T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949647 | |||||||
| chr11:949700 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-9737G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949700 | |||||||
| chr11:949765 | ACT | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-9669_68-9668del others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 949765 | ||||||
| chr11:949781 | G | GA | 157 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.68-9643dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 949781 | ||||||
| chr11:949814 | C | T | 1 | a0001c0002t0004g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68-9623C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949814 | |||||||
| chr11:949843 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.68-9594T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949843 | |||||||
| chr11:949900 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-9537T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949900 | |||||||
| chr11:949967 | C | T | 1 | a0001c0010t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-9470C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949967 | |||||||
| chr11:949981 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-9456A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949981 | |||||||
| chr11:949984 | A | G | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-9453A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 949984 | |||||||
| chr11:950293 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-9144C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950293 | |||||||
| chr11:950311 | G | GT | 34 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0112 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.68-9108dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 950311 | ||||||
| chr11:950510 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-8927G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950510 | |||||||
| chr11:950529 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68-8908C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950529 | |||||||
| chr11:950583 | G | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-8854G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950583 | |||||||
| chr11:950665 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68-8772C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950665 | |||||||
| chr11:950691 | G | A | 4 | a0001c0002t0005g0145 a0001c0002t0005g0146 a0001c0002t0005g0194 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8746G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950691 | |||||||
| chr11:950725 | G | T | 1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.68-8712G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950725 | |||||||
| chr11:950750 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-8687T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 950750 | |||||||
| chr11:951067 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-8370G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951067 | |||||||
| chr11:951127 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.68-8310T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951127 | |||||||
| chr11:951390 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-8047A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951390 | |||||||
| chr11:951526 | C | CA | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-7898dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 951526 | ||||||
| chr11:951540 | G | A | 1 | a0001c0004t0009g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-7897G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951540 | |||||||
| chr11:951558 | C | T | 228 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.68-7879C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951558 | |||||||
| chr11:951928 | GT | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-7508delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 951928 | |||||||
| chr11:951972 | AT | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-7463delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 951972 | ||||||
| chr11:952028 | C | G | 1 | a0001c0003t0002g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.68-7409C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952028 | |||||||
| chr11:952111 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-7326C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952111 | |||||||
| chr11:952207 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-7230A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952207 | |||||||
| chr11:952274 | G | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(13): Show |
16 | HG01978.hp1 HG01981.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-7163G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952274 | |||||||
| chr11:952327 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-7110T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952327 | |||||||
| chr11:952503 | A | G | 1 | a0001c0001t0014g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.68-6934A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952503 | |||||||
| chr11:952509 | T | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-6928T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952509 | |||||||
| chr11:952605 | T | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.68-6832T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952605 | |||||||
| chr11:952797 | C | G | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68-6640C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952797 | |||||||
| chr11:952931 | A | G | 1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-6506A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952931 | |||||||
| chr11:952965 | T | C | 1 | a0001c0002t0002g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68-6472T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 952965 | |||||||
| chr11:953014 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-6423T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953014 | |||||||
| chr11:953096 | C | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-6341C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953096 | |||||||
| chr11:953131 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-6306C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953131 | |||||||
| chr11:953210 | T | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-6227T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953210 | |||||||
| chr11:953308 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-6129G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953308 | |||||||
| chr11:953310 | G | A | 3 | a0001c0003t0002g0135 a0001c0003t0002g0161 a0001c0003t0002g0162 |
3 | HG02572.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-6127G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953310 | |||||||
| chr11:953371 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-6066C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953371 | |||||||
| chr11:953407 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-6030C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953407 | |||||||
| chr11:953545 | G | GC | 37 | a0001c0002t0002g0004 a0001c0002t0002g0133 a0001c0002t0002g0232 others(34): Show |
37 | HG00621.hp2 HG01192.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.68-5880dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953545 | ||||||
| chr11:953551 | C | CA | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-5886_68-5885ins others(1): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953551 | |||||||
| chr11:953618 | G | GCTCCGTC others(3): Show |
2 | a0001c0002t0002g0239 a0001c0003t0002g0237 |
2 | HG04115.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.68-5796_68-5787dup others(10): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953618 | ||||||
| chr11:953618 | GCTCCGTC others(3): Show |
G | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.68-5796_68-5787del others(10): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953618 | ||||||
| chr11:953618 | GCTCCGTC others(13): Show |
G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0035 others(4): Show |
7 | HG01346.hp2 HG01952.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-5806_68-5787del others(20): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953618 | ||||||
| chr11:953620 | TCCGTCTG others(4): Show |
T | 1 | a0001c0001t0001g0017 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.68-5815_68-5805del others(11): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953620 | ||||||
| chr11:953674 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.68-5763T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953674 | |||||||
| chr11:953686 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-5751G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953686 | |||||||
| chr11:953785 | C | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-5652C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953785 | |||||||
| chr11:953837 | C | CT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01346.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-5585dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 953837 | ||||||
| chr11:953898 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-5539G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953898 | |||||||
| chr11:953921 | G | T | 1 | a0001c0002t0002g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-5516G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953921 | |||||||
| chr11:953953 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-5484A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 953953 | |||||||
| chr11:954025 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-5412A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954025 | |||||||
| chr11:954050 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.68-5387G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954050 | |||||||
| chr11:954111 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-5326T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954111 | |||||||
| chr11:954434 | A | G | 10 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0243 others(7): Show |
10 | HG00597.hp2 HG00621.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-5003A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954434 | |||||||
| chr11:954576 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.68-4861A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954576 | |||||||
| chr11:954586 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.68-4851G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954586 | |||||||
| chr11:954615 | A | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-4822A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 954615 | |||||||
| chr11:954722 | G | GGT | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-4700_68-4699dup others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 954722 | ||||||
| chr11:955019 | C | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-4418C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955019 | |||||||
| chr11:955041 | A | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-4396A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955041 | |||||||
| chr11:955093 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.68-4344A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955093 | |||||||
| chr11:955094 | G | A | 58 | a0001c0002t0002g0155 a0001c0002t0002g0160 a0001c0002t0002g0163 others(55): Show |
58 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.68-4343G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955094 | |||||||
| chr11:955360 | C | T | 1 | a0001c0001t0007g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-4077C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955360 | |||||||
| chr11:955372 | G | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-4065G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955372 | |||||||
| chr11:955636 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3801C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955636 | |||||||
| chr11:955638 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-3799G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955638 | |||||||
| chr11:955868 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.68-3569G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 955868 | |||||||
| chr11:956075 | C | G | 10 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0143 others(7): Show |
10 | HG00741.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-3362C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956075 | |||||||
| chr11:956270 | C | T | 1 | a0001c0001t0007g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-3167C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956270 | |||||||
| chr11:956276 | T | G | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68-3161T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956276 | |||||||
| chr11:956312 | G | A | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-3125G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956312 | |||||||
| chr11:956319 | C | T | 5 | a0001c0003t0002g0134 a0001c0003t0002g0197 a0001c0003t0002g0207 others(2): Show |
5 | HG00544.hp2 NA18944.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-3118C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956319 | |||||||
| chr11:956421 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.68-3016G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956421 | |||||||
| chr11:956509 | A | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
12 | HG02056.hp1 HG02132.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-2928A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956509 | |||||||
| chr11:956601 | T | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-2836T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956601 | |||||||
| chr11:956603 | A | G | 1 | a0001c0002t0004g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68-2834A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956603 | |||||||
| chr11:956761 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-2676G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 956761 | |||||||
| chr11:957220 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.68-2217C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957220 | |||||||
| chr11:957245 | C | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-2192C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957245 | |||||||
| chr11:957271 | C | G | 1 | a0001c0002t0003g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.68-2166C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957271 | |||||||
| chr11:957414 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.68-2023G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957414 | |||||||
| chr11:957540 | C | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-1897C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957540 | |||||||
| chr11:957742 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-1695A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957742 | |||||||
| chr11:957832 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-1605G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 957832 | |||||||
| chr11:958011 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0024 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.68-1426G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958011 | |||||||
| chr11:958175 | G | A | 1 | a0001c0001t0007g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-1262G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958175 | |||||||
| chr11:958288 | C | T | 1 | a0001c0001t0007g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-1149C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958288 | |||||||
| chr11:958336 | G | T | 6 | a0001c0002t0002g0208 a0001c0002t0002g0213 a0001c0003t0002g0137 others(3): Show |
6 | HG00597.hp1 HG02083.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-1101G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958336 | |||||||
| chr11:958384 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-1053C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958384 | |||||||
| chr11:958509 | A | G | 1 | a0001c0001t0005g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.68-928A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958509 | |||||||
| chr11:958527 | C | T | 1 | a0001c0003t0006g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.68-910C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958527 | |||||||
| chr11:958566 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-871A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958566 | |||||||
| chr11:958789 | T | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.68-648T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958789 | |||||||
| chr11:958878 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-559C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958878 | |||||||
| chr11:958915 | G | T | 1 | a0001c0003t0002g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.68-522G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 958915 | |||||||
| chr11:959197 | C | G | 5 | a0001c0002t0004g0222 a0001c0002t0004g0227 a0001c0002t0004g0229 others(2): Show |
5 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-240C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 959197 | |||||||
| chr11:959197 | C | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-240C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 959197 | |||||||
| chr11:959279 | C | T | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.68-158C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 959279 | |||||||
| chr11:959530 | G | GAAATGTC others(11): Show |
1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.136+26_136+43dupAA others(16): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 959530 | ||||||
| chr11:959629 | C | T | 1 | a0001c0002t0003g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.136+124C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 959629 | |||||||
| chr11:959655 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.136+150A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 959655 | |||||||
| chr11:959686 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+181A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 959686 | |||||||
| chr11:959776 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+271C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 959776 | |||||||
| chr11:959811 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.136+306G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 959811 | |||||||
| chr11:960114 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+609C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960114 | |||||||
| chr11:960247 | C | CT | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.136+755dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 960247 | ||||||
| chr11:960305 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.136+800C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960305 | |||||||
| chr11:960512 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136+1007A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960512 | |||||||
| chr11:960566 | C | T | 37 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0141 others(34): Show |
37 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.136+1061C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960566 | |||||||
| chr11:960597 | C | T | 2 | a0001c0001t0007g0106 a0001c0003t0002g0258 |
2 | HG00323.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.136+1092C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960597 | |||||||
| chr11:960640 | C | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+1135C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960640 | |||||||
| chr11:960641 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+1136A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960641 | |||||||
| chr11:960865 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.136+1360G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 960865 | |||||||
| chr11:961046 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.136+1541C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961046 | |||||||
| chr11:961108 | G | A | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1603G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961108 | |||||||
| chr11:961180 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.136+1675C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961180 | |||||||
| chr11:961236 | A | ACCACCAG others(161): Show |
1 | a0001c0001t0001g0074 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136+1764_136+1765i others(170): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961236 | ||||||
| chr11:961268 | T | TGGA | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+1764_136+1765i others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961268 | ||||||
| chr11:961285 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+1780T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961285 | |||||||
| chr11:961341 | G | GTCACCAC others(45): Show |
135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.136+1836_136+1837i others(54): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961341 | |||||||
| chr11:961346 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01071.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.136+1841G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961346 | |||||||
| chr11:961349 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.136+1844A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961349 | |||||||
| chr11:961381 | TGGA | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.136+1878_136+1880d others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961381 | ||||||
| chr11:961382 | G | GATGTGGG others(43): Show |
1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.136+1877_136+1878i others(52): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961382 | |||||||
| chr11:961384 | A | AGATGTGG others(158): Show |
1 | a0001c0001t0001g0056 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.136+1895_136+1896i others(167): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961384 | ||||||
| chr11:961406 | A | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+1901A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961406 | |||||||
| chr11:961411 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+1906T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961411 | |||||||
| chr11:961462 | G | A | 1 | a0001c0003t0008g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.136+1957G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961462 | |||||||
| chr11:961484 | T | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+1979T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961484 | |||||||
| chr11:961527 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+2022C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961527 | |||||||
| chr11:961577 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.136+2072T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961577 | |||||||
| chr11:961578 | G | GCCACCAC others(53): Show |
136 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.136+2079_136+2080i others(62): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961578 | ||||||
| chr11:961578 | G | GCCACCAG others(282): Show |
1 | a0001c0001t0001g0074 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136+2124_136+2125i others(291): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961578 | ||||||
| chr11:961597 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.136+2092G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961597 | |||||||
| chr11:961657 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+2152G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961657 | |||||||
| chr11:961714 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+2209G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961714 | |||||||
| chr11:961740 | T | C | 152 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.136+2235T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961740 | |||||||
| chr11:961740 | TAGTCGCC others(52): Show |
T | 1 | a0001c0005t0003g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136+2248_136+2306d others(61): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 961740 | ||||||
| chr11:961812 | G | C | 2 | a0001c0002t0002g0147 a0001c0002t0005g0146 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136+2307G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961812 | |||||||
| chr11:961858 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.136+2353G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961858 | |||||||
| chr11:961865 | C | T | 2 | a0001c0003t0002g0162 a0001c0004t0010g0169 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.136+2360C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961865 | |||||||
| chr11:961889 | G | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.136+2384G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961889 | |||||||
| chr11:961970 | C | G | 1 | a0001c0002t0002g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.136+2465C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 961970 | |||||||
| chr11:962005 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+2500G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962005 | |||||||
| chr11:962078 | G | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.136+2573G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962078 | |||||||
| chr11:962150 | T | TG | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2650dupG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 962150 | ||||||
| chr11:962190 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.136+2685T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962190 | |||||||
| chr11:962326 | C | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+2821C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962326 | |||||||
| chr11:962357 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2852G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962357 | |||||||
| chr11:962390 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.136+2885A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962390 | |||||||
| chr11:962598 | A | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+3093A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962598 | |||||||
| chr11:962642 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+3137A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962642 | |||||||
| chr11:962647 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0051 |
3 | HG02622.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.136+3142C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962647 | |||||||
| chr11:962681 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+3176C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962681 | |||||||
| chr11:962723 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.136+3218A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962723 | |||||||
| chr11:962745 | A | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+3240A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962745 | |||||||
| chr11:962794 | C | CATGCCTG others(52): Show |
1 | a0001c0001t0001g0111 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.136+3290_136+3348d others(61): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 962794 | ||||||
| chr11:962872 | G | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.136+3367G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 962872 | |||||||
| chr11:963133 | G | GA | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.136+3637dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 963133 | ||||||
| chr11:963267 | G | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.136+3762G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 963267 | |||||||
| chr11:963855 | G | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+4350G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 963855 | |||||||
| chr11:963863 | A | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+4358A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 963863 | |||||||
| chr11:963936 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+4431T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 963936 | |||||||
| chr11:963980 | A | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+4475A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 963980 | |||||||
| chr11:964009 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.136+4504C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964009 | |||||||
| chr11:964271 | C | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+4766C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964271 | |||||||
| chr11:964476 | A | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.136+4971A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964476 | |||||||
| chr11:964700 | A | C | 2 | a0001c0003t0002g0136 a0001c0003t0002g0215 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+5195A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964700 | |||||||
| chr11:964755 | G | T | 1 | a0001c0002t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.136+5250G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964755 | |||||||
| chr11:964776 | C | CAAAGGAA others(229): Show |
1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(238): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(1173): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.136+5301_136+5302i others(1182): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5008): Show |
1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5017): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0001g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4536): Show |
1 | a0001c0001t0001g0094 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4545): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4418): Show |
1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4427): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5362): Show |
1 | a0001c0012t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5371): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(3120): Show |
1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(3129): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
1 | a0001c0001t0005g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4654): Show |
1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4663): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(642): Show |
1 | a0001c0002t0004g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(651): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5244): Show |
1 | a0001c0001t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5253): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(701): Show |
1 | a0001c0001t0001g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(710): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(819): Show |
2 | a0001c0001t0001g0033 a0001c0006t0001g0044 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.136+5301_136+5302i others(828): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4890): Show |
1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4899): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4831): Show |
1 | a0001c0001t0001g0035 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4840): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4418): Show |
1 | a0001c0001t0001g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4427): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4536): Show |
1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4545): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4654): Show |
1 | a0001c0001t0001g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4663): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
1 | a0001c0001t0001g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | NA18962.hp2 NA18986.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(1822): Show |
8 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+5301_136+5302i others(1831): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4713): Show |
1 | a0001c0001t0002g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4722): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(3356): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0122 |
2 | NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.136+5301_136+5302i others(3365): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
18 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0051 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5124): Show |
1 | a0001c0001t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5133): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0001g0025 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5126): Show |
1 | a0001c0001t0001g0026 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5135): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0001g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5185): Show |
1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5194): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0001g0056 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4005): Show |
1 | a0001c0001t0001g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4014): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4713): Show |
1 | a0001c0001t0001g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4722): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(5067): Show |
1 | a0001c0001t0016g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(5076): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4831): Show |
1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4840): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(1999): Show |
1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(2008): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(3887): Show |
1 | a0001c0001t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(3896): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4890): Show |
1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4899): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(465): Show |
1 | a0001c0001t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(474): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4418): Show |
1 | a0001c0001t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4427): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(1822): Show |
1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(1831): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4713): Show |
1 | a0001c0001t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4722): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(29): Show |
32 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(760): Show |
1 | a0001c0001t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.136+5301_136+5302i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4949): Show |
1 | a0001c0001t0001g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4958): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4949): Show |
1 | a0001c0001t0001g0017 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4958): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964776 | C | CAAAGGAA others(4536): Show |
1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.136+5301_136+5302i others(4545): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964776 | ||||||
| chr11:964807 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.136+5302A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964807 | |||||||
| chr11:964808 | A | ATGGAAAG others(4831): Show |
1 | a0001c0002t0005g0146 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136+5322_136+5323i others(4840): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964808 | ||||||
| chr11:964808 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.136+5303A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964808 | |||||||
| chr11:964823 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136+5318C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964823 | |||||||
| chr11:964828 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.136+5323A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964828 | |||||||
| chr11:964867 | A | ATGGAAAG others(1759): Show |
1 | a0001c0001t0003g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(1768): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2762): Show |
1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2771): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2585): Show |
1 | a0001c0001t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2594): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2408): Show |
1 | a0001c0001t0014g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2417): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2585): Show |
4 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0006t0001g0127 others(1): Show |
4 | HG01109.hp1 HG02523.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-5224_137-5223i others(2594): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2644): Show |
1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2653): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2294): Show |
1 | a0001c0002t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2303): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2648): Show |
1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137-5224_137-5223i others(2657): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3887): Show |
1 | a0001c0002t0002g0208 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3896): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(642): Show |
2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(651): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(701): Show |
1 | a0001c0002t0002g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(710): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3936): Show |
1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3945): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3936): Show |
1 | a0001c0003t0002g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3945): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3995): Show |
1 | a0001c0003t0002g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4004): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(1763): Show |
1 | a0001c0002t0003g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(1772): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(1881): Show |
1 | a0001c0002t0003g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(1890): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2058): Show |
1 | a0001c0005t0003g0181 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2067): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2353): Show |
1 | a0001c0002t0003g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2362): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2471): Show |
4 | a0001c0002t0003g0142 a0001c0002t0003g0152 a0001c0002t0003g0201 others(1): Show |
4 | HG00741.hp2 HG02165.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5126_137-5125i others(2480): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2530): Show |
5 | a0001c0002t0003g0141 a0001c0002t0003g0153 a0001c0002t0003g0176 others(2): Show |
5 | HG01358.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-5126_137-5125i others(2539): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2589): Show |
10 | a0001c0002t0003g0173 a0001c0002t0003g0175 a0001c0002t0003g0177 others(7): Show |
10 | HG00558.hp1 HG01099.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-5126_137-5125i others(2598): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2648): Show |
2 | a0001c0002t0003g0151 a0001c0015t0003g0174 |
2 | HG00609.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(2657): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2825): Show |
1 | a0001c0002t0004g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2834): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2884): Show |
1 | a0001c0002t0002g0239 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2893): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4005): Show |
1 | a0001c0002t0003g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4014): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4300): Show |
1 | a0001c0010t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4309): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4418): Show |
1 | a0001c0002t0002g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4427): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4241): Show |
2 | a0001c0003t0002g0136 a0001c0003t0002g0215 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(4250): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2825): Show |
1 | a0001c0003t0002g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2834): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3877): Show |
2 | a0001c0003t0002g0197 a0001c0003t0002g0209 |
2 | NA18944.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(3886): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4408): Show |
3 | a0001c0003t0002g0211 a0001c0003t0002g0216 a0001c0003t0002g0217 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(4417): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4349): Show |
1 | a0001c0003t0002g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4358): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4349): Show |
1 | a0001c0003t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4358): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4821): Show |
1 | a0001c0003t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4830): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3228): Show |
1 | a0001c0002t0002g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3237): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4880): Show |
2 | a0001c0002t0002g0246 a0001c0002t0002g0250 |
2 | NA18990.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(4889): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4467): Show |
1 | a0001c0002t0002g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4476): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4526): Show |
1 | a0001c0002t0002g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4535): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4467): Show |
1 | a0001c0002t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4476): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4113): Show |
1 | a0001c0002t0002g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4762): Show |
1 | a0001c0002t0002g0247 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4771): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4939): Show |
1 | a0001c0002t0002g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4948): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4939): Show |
1 | a0001c0002t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4948): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4880): Show |
1 | a0001c0002t0002g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4889): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4939): Show |
1 | a0001c0002t0002g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4948): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4880): Show |
2 | a0001c0002t0002g0167 a0001c0002t0002g0248 |
2 | HG01981.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(4889): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4919): Show |
1 | a0005c0011t0002g0242 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4928): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2589): Show |
1 | a0001c0002t0003g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2598): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4703): Show |
1 | a0001c0003t0002g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4712): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4408): Show |
1 | a0001c0002t0002g0241 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4417): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4349): Show |
2 | a0001c0002t0002g0164 a0001c0002t0002g0165 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(4358): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3946): Show |
1 | a0001c0002t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3955): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2176): Show |
2 | a0001c0002t0003g0180 a0001c0002t0003g0191 |
2 | HG01081.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(2185): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2530): Show |
1 | a0001c0002t0003g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2539): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2589): Show |
1 | a0001c0005t0003g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2598): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4762): Show |
1 | a0001c0002t0002g0243 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4771): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4644): Show |
1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4653): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4536): Show |
1 | a0001c0003t0002g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4545): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2471): Show |
1 | a0001c0003t0006g0267 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2480): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3002): Show |
1 | a0001c0003t0006g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3011): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3061): Show |
2 | a0001c0003t0006g0263 a0001c0003t0006g0266 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-5126_137-5125i others(3070): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4241): Show |
1 | a0001c0002t0005g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4250): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4654): Show |
1 | a0001c0003t0006g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4663): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4408): Show |
1 | a0001c0003t0002g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4417): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3946): Show |
1 | a0001c0002t0005g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3955): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4349): Show |
1 | a0001c0002t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4358): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3297): Show |
1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(3306): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2471): Show |
1 | a0001c0002t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137-5067_137-5066i others(2480): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2589): Show |
3 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0005t0003g0144 |
3 | HG00621.hp1 HG03927.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.137-5067_137-5066i others(2598): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4880): Show |
1 | a0001c0002t0002g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.137-5067_137-5066i others(4889): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(4467): Show |
1 | a0001c0001t0005g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-5067_137-5066i others(4476): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2589): Show |
1 | a0001c0003t0008g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.137-5067_137-5066i others(2598): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(3936): Show |
1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.137-5067_137-5066i others(3945): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | ATGGAAAG others(2590): Show |
1 | a0001c0003t0008g0193 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.137-5256_137-5255i others(2599): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964867 | ||||||
| chr11:964867 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-5302A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964867 | |||||||
| chr11:964887 | G | GGGAAATT others(4939): Show |
1 | a0001c0002t0002g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(4948): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964887 | ||||||
| chr11:964945 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0002g0054 |
2 | HG03834.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.137-5224C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964945 | |||||||
| chr11:964985 | G | GTGGAAAG others(170): Show |
4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-5126_137-5125i others(179): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(229): Show |
11 | a0001c0002t0002g0213 a0001c0003t0002g0134 a0001c0003t0002g0137 others(8): Show |
11 | HG00544.hp2 HG00597.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.137-5126_137-5125i others(238): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(5008): Show |
1 | a0001c0003t0006g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(5017): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(4998): Show |
1 | a0001c0002t0002g0244 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(5007): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(7180): Show |
1 | a0001c0002t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(7189): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(1881): Show |
1 | a0001c0004t0009g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.137-5126_137-5125i others(1890): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:964985 | G | GTGGAAAG others(1999): Show |
1 | a0001c0004t0009g0259 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.137-5126_137-5125i others(2008): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 964985 | ||||||
| chr11:965000 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0122 |
2 | NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.137-5169C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965000 | |||||||
| chr11:965004 | C | T | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0131 others(2): Show |
5 | HG01109.hp1 HG02129.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-5165C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965004 | |||||||
| chr11:965044 | G | A | 3 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0006t0018g0100 |
3 | HG02055.hp1 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.137-5125G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965044 | |||||||
| chr11:965044 | G | GTGGAAAG others(170): Show |
8 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-4949_137-4948i others(179): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965044 | ||||||
| chr11:965057 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0105 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.137-5112A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965057 | |||||||
| chr11:965072 | A | AAAGGAAA others(5006): Show |
1 | a0001c0001t0001g0027 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.137-5067_137-5066i others(5015): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965072 | ||||||
| chr11:965103 | G | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-5066G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965103 | |||||||
| chr11:965154 | G | A | 3 | a0001c0002t0002g0243 a0001c0002t0002g0247 a0005c0011t0002g0242 |
3 | NA18964.hp2 NA18969.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.137-5015G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965154 | |||||||
| chr11:965162 | G | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG01243.hp2 HG02055.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-5007G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965162 | |||||||
| chr11:965181 | C | CGGGAAAT others(1232): Show |
1 | a0002c0007t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.137-4949_137-4948i others(1241): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965181 | ||||||
| chr11:965181 | C | CGGGAAAT others(819): Show |
2 | a0001c0002t0004g0228 a0001c0002t0004g0252 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.137-4949_137-4948i others(828): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965181 | ||||||
| chr11:965181 | C | CGGGAAAT others(760): Show |
3 | a0001c0002t0004g0226 a0001c0002t0004g0253 a0001c0002t0004g0254 |
3 | HG02886.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.137-4949_137-4948i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965181 | ||||||
| chr11:965181 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.137-4988C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965181 | |||||||
| chr11:965201 | T | C | 13 | a0001c0002t0002g0208 a0001c0003t0002g0136 a0001c0003t0002g0197 others(10): Show |
13 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-4968T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965201 | |||||||
| chr11:965201 | T | TCCCAGAT others(4757): Show |
1 | a0001c0003t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137-4882_137-4881i others(4766): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(7073): Show |
1 | a0001c0003t0002g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(7082): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(4821): Show |
4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-4882_137-4881i others(4830): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(4821): Show |
1 | a0001c0003t0002g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(4830): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(6178): Show |
1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(6187): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(4762): Show |
3 | a0001c0002t0002g0213 a0001c0003t0002g0137 a0001c0003t0002g0199 |
3 | HG00597.hp1 HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.137-4882_137-4881i others(4771): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(8597): Show |
1 | a0001c0003t0002g0134 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(8606): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(4762): Show |
1 | a0001c0003t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-4882_137-4881i others(4771): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(9127): Show |
1 | a0001c0003t0002g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(9136): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965201 | T | TCCCAGAT others(7035): Show |
1 | a0001c0003t0002g0221 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.137-4882_137-4881i others(7044): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965201 | ||||||
| chr11:965240 | C | CGGGAAAT others(5834): Show |
1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(5843): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | CGGGAAAT others(6778): Show |
1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.137-4882_137-4881i others(6787): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | CGGGAAAT others(3828): Show |
1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.137-4882_137-4881i others(3837): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | CGGGAAAT others(2884): Show |
1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.137-4882_137-4881i others(2893): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | CGGGAAAT others(760): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | NA18952.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.137-4882_137-4881i others(769): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | CGGGAAAT others(111): Show |
6 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(3): Show |
6 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-4882_137-4881i others(120): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965240 | ||||||
| chr11:965240 | C | T | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.137-4929C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965240 | |||||||
| chr11:965288 | A | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.137-4881A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965288 | |||||||
| chr11:965289 | A | ATGGAACG others(2352): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.137-4875_137-4874i others(2361): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 965289 | ||||||
| chr11:965308 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | NA18950.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.137-4861G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965308 | |||||||
| chr11:965350 | A | G | 1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137-4819A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965350 | |||||||
| chr11:965581 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.137-4588C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965581 | |||||||
| chr11:965606 | T | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.137-4563T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965606 | |||||||
| chr11:965671 | C | T | 4 | a0001c0001t0005g0156 a0001c0002t0002g0133 a0001c0002t0002g0158 others(1): Show |
4 | HG01884.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-4498C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965671 | |||||||
| chr11:965713 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.137-4456G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965713 | |||||||
| chr11:965911 | A | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0076 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-4258A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965911 | |||||||
| chr11:965944 | C | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-4225C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 965944 | |||||||
| chr11:966181 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-3988T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966181 | |||||||
| chr11:966386 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-3783C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966386 | |||||||
| chr11:966609 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0056 a0001c0001t0001g0094 |
3 | HG00140.hp2 HG01071.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-3560C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966609 | |||||||
| chr11:966620 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0002t0001g0071 |
3 | HG01934.hp2 HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.137-3549C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966620 | |||||||
| chr11:966813 | G | A | 14 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.137-3356G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966813 | |||||||
| chr11:966813 | G | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-3356G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966813 | |||||||
| chr11:966951 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.137-3218G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 966951 | |||||||
| chr11:967023 | T | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.137-3146T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967023 | |||||||
| chr11:967268 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-2901T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967268 | |||||||
| chr11:967349 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.137-2820G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967349 | |||||||
| chr11:967461 | A | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-2708A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967461 | |||||||
| chr11:967659 | C | T | 7 | a0001c0002t0004g0222 a0001c0002t0004g0223 a0001c0002t0004g0227 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-2510C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967659 | |||||||
| chr11:967822 | C | T | 6 | a0001c0001t0003g0103 a0001c0001t0005g0082 a0001c0001t0005g0083 others(3): Show |
6 | HG01258.hp1 HG01261.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-2347C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967822 | |||||||
| chr11:967943 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.137-2226T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967943 | |||||||
| chr11:967944 | A | G | 4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-2225A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 967944 | |||||||
| chr11:968080 | C | G | 1 | a0001c0002t0002g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.137-2089C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968080 | |||||||
| chr11:968118 | C | T | 6 | a0001c0002t0002g0208 a0001c0002t0002g0213 a0001c0003t0002g0137 others(3): Show |
6 | HG00597.hp1 HG02083.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-2051C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968118 | |||||||
| chr11:968356 | C | T | 10 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0143 others(7): Show |
10 | HG00741.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-1813C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968356 | |||||||
| chr11:968432 | TCCCATCC others(5): Show |
T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.137-1736_137-1725d others(14): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968432 | |||||||
| chr11:968433 | C | T | 147 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(144): Show |
147 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.137-1736C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968433 | |||||||
| chr11:968453 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.137-1716C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968453 | |||||||
| chr11:968472 | C | T | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.137-1697C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968472 | |||||||
| chr11:968579 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-1590G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968579 | |||||||
| chr11:968610 | G | T | 1 | a0001c0002t0003g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.137-1559G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968610 | |||||||
| chr11:968712 | C | T | 4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-1457C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968712 | |||||||
| chr11:968731 | C | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-1438C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968731 | |||||||
| chr11:968874 | G | T | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-1295G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 968874 | |||||||
| chr11:969065 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.137-1104C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969065 | |||||||
| chr11:969087 | A | C | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.137-1082A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969087 | |||||||
| chr11:969216 | A | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.137-953A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969216 | |||||||
| chr11:969219 | CCTTT | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0028 others(14): Show |
17 | HG00423.hp1 HG00673.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.137-949_137-946del others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969219 | |||||||
| chr11:969219 | CCTTTT | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.137-949_137-945del others(5): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969219 | |||||||
| chr11:969219 | CCTTTTT | C | 20 | a0001c0001t0001g0061 a0001c0002t0002g0225 a0001c0002t0002g0232 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-949_137-944del others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969219 | |||||||
| chr11:969220 | C | CT | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(23): Show |
26 | HG00544.hp2 HG01081.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-922dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 969220 | ||||||
| chr11:969220 | CT | C | 19 | a0001c0002t0002g0155 a0001c0002t0002g0163 a0001c0002t0002g0165 others(16): Show |
19 | HG00597.hp2 HG00621.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.137-922delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 969220 | ||||||
| chr11:969517 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-652T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969517 | |||||||
| chr11:969675 | C | T | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.137-494C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969675 | |||||||
| chr11:969818 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-351C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969818 | |||||||
| chr11:969830 | G | C | 2 | a0001c0002t0004g0228 a0001c0002t0004g0252 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.137-339G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 969830 | |||||||
| chr11:970029 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.137-140C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 970029 | |||||||
| chr11:970042 | G | A | 1 | a0001c0004t0002g0195 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.137-127G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 970042 | |||||||
| chr11:970320 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+9C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970320 | |||||||
| chr11:970372 | C | T | 1 | a0001c0010t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.279+61C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970372 | |||||||
| chr11:970373 | G | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.279+62G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970373 | |||||||
| chr11:970379 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.279+68C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970379 | |||||||
| chr11:970405 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.279+94G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970405 | |||||||
| chr11:970490 | C | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.279+179C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970490 | |||||||
| chr11:970503 | C | T | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.279+192C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970503 | |||||||
| chr11:970510 | G | T | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.279+199G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970510 | |||||||
| chr11:970607 | T | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.279+296T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970607 | |||||||
| chr11:970608 | G | A | 1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+297G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970608 | |||||||
| chr11:970643 | G | A | 4 | a0001c0001t0005g0156 a0001c0002t0002g0133 a0001c0002t0002g0158 others(1): Show |
4 | HG01884.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+332G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970643 | |||||||
| chr11:970818 | C | T | 4 | a0001c0001t0005g0156 a0001c0002t0002g0133 a0001c0002t0002g0158 others(1): Show |
4 | HG01884.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+507C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970818 | |||||||
| chr11:970847 | C | T | 10 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0143 others(7): Show |
10 | HG00741.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+536C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 970847 | |||||||
| chr11:971166 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.279+855T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971166 | |||||||
| chr11:971330 | C | T | 1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.280-732C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971330 | |||||||
| chr11:971408 | G | C | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.280-654G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971408 | |||||||
| chr11:971436 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0051 |
3 | HG02622.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.280-626G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971436 | |||||||
| chr11:971601 | G | A | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(118): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.280-461G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971601 | |||||||
| chr11:971667 | T | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.280-395T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971667 | |||||||
| chr11:971668 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.280-394G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971668 | |||||||
| chr11:971674 | G | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.280-388G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971674 | |||||||
| chr11:971688 | C | T | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-374C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971688 | |||||||
| chr11:971884 | A | G | 4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-178A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 971884 | |||||||
| chr11:972044 | C | T | 1 | a0001c0001t0017g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.280-18C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 3/21 | chr11 | 972044 | |||||||
| chr11:972270 | C | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.473+15C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972270 | |||||||
| chr11:972323 | T | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | NA18952.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.473+68T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972323 | |||||||
| chr11:972433 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.473+178G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972433 | |||||||
| chr11:972439 | A | G | 1 | a0001c0001t0005g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.473+184A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972439 | |||||||
| chr11:972555 | G | T | 1 | a0001c0003t0002g0219 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.473+300G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972555 | |||||||
| chr11:972603 | A | G | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.473+348A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972603 | |||||||
| chr11:972928 | C | T | 1 | a0001c0003t0002g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.473+673C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972928 | |||||||
| chr11:972930 | G | A | 1 | a0001c0002t0002g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.473+675G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 972930 | |||||||
| chr11:973338 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.473+1083A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973338 | |||||||
| chr11:973374 | T | C | 154 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.473+1119T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973374 | |||||||
| chr11:973542 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.473+1287C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973542 | |||||||
| chr11:973577 | T | C | 140 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.473+1322T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973577 | |||||||
| chr11:973628 | G | A | 1 | a0001c0002t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.473+1373G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973628 | |||||||
| chr11:973805 | T | A | 1 | a0001c0002t0004g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.473+1550T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973805 | |||||||
| chr11:973824 | T | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.473+1569T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973824 | |||||||
| chr11:973885 | T | C | 150 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.473+1630T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 973885 | |||||||
| chr11:974035 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.473+1780A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974035 | |||||||
| chr11:974049 | C | G | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+1794C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974049 | |||||||
| chr11:974145 | A | AGGTGGCC others(37): Show |
21 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(18): Show |
21 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.473+1970_473+2013d others(46): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974145 | ||||||
| chr11:974145 | AGGTGGCC others(37): Show |
A | 1 | a0001c0003t0006g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.473+1970_473+2013d others(46): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974145 | ||||||
| chr11:974340 | T | A | 1 | a0001c0002t0003g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.473+2085T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974340 | |||||||
| chr11:974343 | A | C | 1 | a0001c0002t0002g0248 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.473+2088A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974343 | |||||||
| chr11:974508 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.473+2253C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974508 | |||||||
| chr11:974649 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.473+2394C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974649 | |||||||
| chr11:974682 | C | CA | 14 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG00621.hp1 HG01109.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.474-2394dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974682 | ||||||
| chr11:974682 | C | CAAAA | 19 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(16): Show |
19 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.474-2397_474-2394d others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974682 | ||||||
| chr11:974698 | A | AAAAAG | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.474-2394_474-2393i others(7): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974698 | ||||||
| chr11:974698 | A | AAAAG | 6 | a0001c0001t0001g0094 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-2392_474-2389d others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 974698 | ||||||
| chr11:974827 | C | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.474-2268C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974827 | |||||||
| chr11:974899 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.474-2196C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974899 | |||||||
| chr11:974922 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.474-2173T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974922 | |||||||
| chr11:974945 | A | G | 5 | a0001c0002t0003g0201 a0001c0002t0003g0202 a0001c0002t0003g0205 others(2): Show |
5 | HG02027.hp1 HG02165.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-2150A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 974945 | |||||||
| chr11:975194 | G | A | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-1901G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975194 | |||||||
| chr11:975295 | C | T | 1 | a0001c0002t0005g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474-1800C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975295 | |||||||
| chr11:975320 | T | G | 1 | a0001c0001t0007g0040 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.474-1775T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975320 | |||||||
| chr11:975384 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1711G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975384 | |||||||
| chr11:975387 | A | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474-1708A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975387 | |||||||
| chr11:975421 | T | TGTGTGAG others(557): Show |
3 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 |
3 | HG01346.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.474-1653_474-1652i others(566): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975421 | T | TGTGTGAG others(604): Show |
7 | a0001c0002t0004g0226 a0001c0002t0004g0228 a0001c0002t0004g0235 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-1653_474-1652i others(613): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975421 | T | TGTGTGAG others(651): Show |
6 | a0001c0002t0002g0225 a0001c0002t0004g0227 a0001c0002t0004g0229 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-1653_474-1652i others(660): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975421 | T | TGTGTGAG others(745): Show |
2 | a0001c0002t0004g0222 a0001c0002t0004g0223 |
2 | HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.474-1653_474-1652i others(754): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975421 | T | TGTGTGAG others(557): Show |
1 | a0001c0002t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.474-1653_474-1652i others(566): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975421 | T | TGTGTGAG others(557): Show |
1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.474-1653_474-1652i others(566): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975421 | ||||||
| chr11:975437 | G | A | 1 | a0001c0003t0002g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.474-1658G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975437 | |||||||
| chr11:975443 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.474-1652T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975443 | |||||||
| chr11:975481 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1614A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975481 | |||||||
| chr11:975493 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1602T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975493 | |||||||
| chr11:975516 | T | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1579T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975516 | |||||||
| chr11:975518 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1577A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975518 | |||||||
| chr11:975519 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1576C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975519 | |||||||
| chr11:975528 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1567A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975528 | |||||||
| chr11:975530 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1565T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975530 | |||||||
| chr11:975531 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1564A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975531 | |||||||
| chr11:975533 | T | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1562T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975533 | |||||||
| chr11:975541 | A | AGTGGGGT others(134): Show |
14 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.474-1427_474-1426i others(143): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0001g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0001g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0007g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(886): Show |
1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.474-1537_474-1536i others(895): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(933): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0107 |
2 | HG02165.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.474-1537_474-1536i others(942): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
93 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(1027): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0043 others(3): Show |
6 | HG00544.hp1 HG01261.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-1537_474-1536i others(1036): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0087 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(1309): Show |
1 | a0001c0001t0001g0036 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.474-1537_474-1536i others(1318): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | AGTGGGGT others(980): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0117 others(1): Show |
4 | HG00280.hp1 HG00741.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-1537_474-1536i others(989): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | 975541 | ||||||
| chr11:975541 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-1554A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975541 | |||||||
| chr11:975575 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0032 |
2 | HG00544.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.474-1520G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975575 | |||||||
| chr11:975587 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.474-1508C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975587 | |||||||
| chr11:975622 | G | C | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.474-1473G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975622 | |||||||
| chr11:975632 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.474-1463A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975632 | |||||||
| chr11:975669 | C | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.474-1426C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975669 | |||||||
| chr11:975675 | G | A | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-1420G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975675 | |||||||
| chr11:975712 | C | T | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.474-1383C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975712 | |||||||
| chr11:975713 | G | T | 5 | a0001c0003t0002g0203 a0001c0003t0002g0211 a0001c0003t0002g0216 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1382G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975713 | |||||||
| chr11:975715 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.474-1380C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975715 | |||||||
| chr11:975735 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.474-1360A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975735 | |||||||
| chr11:976019 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.474-1076G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976019 | |||||||
| chr11:976351 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.474-744C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976351 | |||||||
| chr11:976565 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.474-530T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976565 | |||||||
| chr11:976614 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.474-481T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976614 | |||||||
| chr11:976677 | T | C | 151 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(148): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.474-418T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976677 | |||||||
| chr11:976964 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-131G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976964 | |||||||
| chr11:976990 | C | T | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-105C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 976990 | |||||||
| chr11:977036 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.474-59C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 977036 | |||||||
| chr11:977253 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.603+29G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977253 | |||||||
| chr11:977322 | A | T | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.603+98A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977322 | |||||||
| chr11:977511 | C | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.603+287C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977511 | |||||||
| chr11:977673 | T | G | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.603+449T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977673 | |||||||
| chr11:977679 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+455G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977679 | |||||||
| chr11:977682 | C | G | 146 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.603+458C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977682 | |||||||
| chr11:977685 | G | A | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.603+461G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977685 | |||||||
| chr11:977715 | C | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.603+491C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977715 | |||||||
| chr11:977743 | C | T | 1 | a0001c0002t0002g0250 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.603+519C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 977743 | |||||||
| chr11:978087 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.603+863C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978087 | |||||||
| chr11:978148 | A | G | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.603+924A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978148 | |||||||
| chr11:978166 | G | A | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.603+942G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978166 | |||||||
| chr11:978194 | C | T | 1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.603+970C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978194 | |||||||
| chr11:978217 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.603+993C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978217 | |||||||
| chr11:978219 | G | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.603+995G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978219 | |||||||
| chr11:978242 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.603+1018G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978242 | |||||||
| chr11:978289 | C | T | 6 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0244 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.603+1065C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978289 | |||||||
| chr11:978526 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.603+1302T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978526 | |||||||
| chr11:978612 | T | C | 2 | a0001c0002t0002g0241 a0001c0002t0002g0257 |
2 | HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.603+1388T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978612 | |||||||
| chr11:978661 | G | A | 1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.603+1437G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978661 | |||||||
| chr11:978921 | C | T | 4 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+1697C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 978921 | |||||||
| chr11:979124 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.603+1900G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979124 | |||||||
| chr11:979202 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.603+1978C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979202 | |||||||
| chr11:979262 | G | C | 1 | a0001c0001t0019g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.604-1936G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979262 | |||||||
| chr11:979376 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.604-1822C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979376 | |||||||
| chr11:979511 | G | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.604-1687G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979511 | |||||||
| chr11:979650 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.604-1548C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979650 | |||||||
| chr11:979664 | C | T | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.604-1534C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979664 | |||||||
| chr11:979665 | G | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.604-1533G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979665 | |||||||
| chr11:979804 | G | T | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.604-1394G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979804 | |||||||
| chr11:979845 | C | G | 1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.604-1353C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 979845 | |||||||
| chr11:980013 | C | CTGTCCTG others(92): Show |
1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.604-1160_604-1159i others(101): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980013 | ||||||
| chr11:980027 | T | C | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.604-1171T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980027 | |||||||
| chr11:980058 | G | A | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.604-1140G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980058 | |||||||
| chr11:980060 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-1138T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980060 | |||||||
| chr11:980067 | CTGCCCGG others(422): Show |
C | 10 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
10 | HG01109.hp1 HG02083.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.604-1054_604-626de others(1): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980067 | ||||||
| chr11:980093 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-1105T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980093 | |||||||
| chr11:980100 | C | CTGCCCGG others(1313): Show |
1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.604-934_604-933ins others(1320): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1082): Show |
3 | a0001c0003t0002g0006 a0001c0003t0002g0210 a0001c0003t0002g0219 |
3 | HG02523.hp2 HG02738.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1049): Show |
1 | a0001c0003t0002g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1049): Show |
2 | a0001c0003t0002g0197 a0001c0003t0002g0214 |
2 | NA18944.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.604-967_604-966ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1082): Show |
3 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 |
3 | HG01069.hp2 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1082): Show |
1 | a0001c0002t0012g0001 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1082): Show |
4 | a0001c0002t0002g0213 a0001c0003t0002g0137 a0001c0003t0002g0199 others(1): Show |
4 | HG00597.hp1 HG02083.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | C | CTGCCCGG others(1247): Show |
1 | a0001c0002t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.604-1000_604-999in others(1255): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980100 | CTGCCCGG others(389): Show |
C | 36 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0141 others(33): Show |
36 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.604-1021_604-626de others(1): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980100 | ||||||
| chr11:980126 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-1072T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980126 | |||||||
| chr11:980133 | C | CTGCCCGG others(653): Show |
1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(660): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1115): Show |
1 | a0001c0002t0002g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(1122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1082): Show |
1 | a0001c0001t0005g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1082): Show |
3 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 |
3 | HG02055.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.604-934_604-933ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1049): Show |
1 | a0001c0002t0005g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-934_604-933ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1082): Show |
1 | a0001c0003t0006g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1049): Show |
1 | a0001c0003t0006g0266 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1049): Show |
1 | a0001c0002t0002g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.604-1000_604-999in others(1057): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1016): Show |
1 | a0001c0002t0002g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.604-1000_604-999in others(1024): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | CTGCCCGG others(1082): Show |
1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.604-1000_604-999in others(1090): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980133 | ||||||
| chr11:980133 | C | G | 1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.604-1065C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980133 | |||||||
| chr11:980159 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-1039T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980159 | |||||||
| chr11:980166 | C | CTGCCCGG others(1115): Show |
1 | a0001c0004t0009g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980166 | ||||||
| chr11:980166 | C | CTGCCCGG others(1016): Show |
1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1023): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980166 | ||||||
| chr11:980167 | T | TGCCCGGT others(1082): Show |
1 | a0001c0010t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.604-934_604-933ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980167 | ||||||
| chr11:980172 | G | GGTGCCGT others(1048): Show |
1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(1055): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980172 | ||||||
| chr11:980192 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-1006T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980192 | |||||||
| chr11:980199 | C | CTGCCCGG others(356): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.604-802_604-801ins others(363): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980199 | ||||||
| chr11:980199 | C | CTGCCCGG others(26): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.604-967_604-966ins others(33): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980199 | ||||||
| chr11:980199 | C | CTGCCCGG others(1016): Show |
1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1023): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980199 | ||||||
| chr11:980199 | C | GTGCCCGG others(1049): Show |
1 | a0001c0003t0006g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.604-1000_604-999in others(1057): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980199 | |||||||
| chr11:980199 | C | GTGCCCGG others(1082): Show |
1 | a0001c0002t0004g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.604-1000_604-999in others(1090): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980199 | |||||||
| chr11:980225 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-973T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980225 | |||||||
| chr11:980232 | C | CTGCCCGG others(455): Show |
1 | a0001c0012t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980232 | ||||||
| chr11:980232 | C | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(31): Show |
34 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.604-966C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1016): Show |
4 | a0001c0002t0002g0241 a0001c0002t0002g0246 a0001c0002t0002g0250 others(1): Show |
4 | HG02027.hp2 NA18990.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-967_604-966ins others(1023): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1049): Show |
1 | a0001c0003t0002g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1082): Show |
1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1016): Show |
1 | a0001c0002t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(1023): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1049): Show |
6 | a0001c0002t0001g0071 a0001c0002t0002g0155 a0001c0002t0002g0163 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-967_604-966ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(950): Show |
1 | a0001c0003t0002g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.604-967_604-966ins others(957): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1082): Show |
4 | a0001c0002t0002g0150 a0001c0003t0006g0263 a0001c0003t0006g0264 others(1): Show |
4 | HG02976.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(884): Show |
1 | a0001c0003t0002g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(891): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1016): Show |
1 | a0001c0002t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1023): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980232 | C | GTGCCCGG others(1082): Show |
1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.604-967_604-966ins others(1089): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980232 | |||||||
| chr11:980258 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-940T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980258 | |||||||
| chr11:980265 | C | CTGCCCGG others(455): Show |
1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980265 | ||||||
| chr11:980265 | C | CTGCCCGG others(455): Show |
1 | a0001c0001t0001g0074 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980265 | ||||||
| chr11:980291 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-907T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980291 | |||||||
| chr11:980298 | C | CTGCCCGG others(488): Show |
1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(495): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(455): Show |
1 | a0001c0001t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(488): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0081 |
2 | HG03492.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.604-802_604-801ins others(495): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(455): Show |
1 | a0001c0001t0016g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(455): Show |
57 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(455): Show |
1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(422): Show |
1 | a0001c0001t0003g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(429): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(422): Show |
19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0023 others(16): Show |
19 | HG02056.hp1 HG02132.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.604-802_604-801ins others(429): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(389): Show |
1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(396): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(389): Show |
3 | a0001c0001t0001g0061 a0001c0001t0005g0088 a0001c0001t0015g0062 |
3 | HG01106.hp2 NA18747.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.604-802_604-801ins others(396): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1148): Show |
2 | a0001c0003t0002g0136 a0001c0003t0002g0215 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.604-769_604-768ins others(1155): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1049): Show |
1 | a0001c0002t0002g0208 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.604-769_604-768ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1049): Show |
6 | a0001c0003t0002g0203 a0001c0003t0002g0204 a0001c0003t0002g0211 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-769_604-768ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1049): Show |
1 | a0001c0003t0002g0134 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.604-835_604-834ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1049): Show |
2 | a0001c0003t0002g0207 a0001c0003t0002g0221 |
2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.604-835_604-834ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | CTGCCCGG others(1049): Show |
1 | a0001c0003t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.604-835_604-834ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980298 | ||||||
| chr11:980298 | C | G | 15 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(12): Show |
15 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.604-900C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980298 | |||||||
| chr11:980324 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-874T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980324 | |||||||
| chr11:980331 | C | CTGCCCGG others(257): Show |
1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(264): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980331 | ||||||
| chr11:980331 | C | CTGCCCGG others(422): Show |
3 | a0001c0001t0007g0089 a0001c0001t0007g0106 a0001c0001t0019g0021 |
3 | HG00323.hp1 HG00738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.604-802_604-801ins others(429): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980331 | ||||||
| chr11:980331 | C | CTGCCCGG others(389): Show |
4 | a0001c0001t0001g0120 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
4 | HG00280.hp2 HG01099.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-802_604-801ins others(396): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980331 | ||||||
| chr11:980331 | C | CTGCCCGG others(389): Show |
1 | a0001c0001t0007g0040 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(396): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980331 | ||||||
| chr11:980331 | C | CTGCCCGG others(356): Show |
1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.604-802_604-801ins others(363): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980331 | ||||||
| chr11:980331 | C | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(9): Show |
12 | HG00642.hp2 HG01943.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-867C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980331 | |||||||
| chr11:980357 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-841T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980357 | |||||||
| chr11:980364 | C | CTGCCCGG others(1445): Show |
2 | a0001c0002t0004g0222 a0001c0002t0004g0227 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.604-809_604-808ins others(1452): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980364 | ||||||
| chr11:980364 | C | CTGCCCGG others(356): Show |
1 | a0001c0001t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(363): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980364 | ||||||
| chr11:980364 | C | G | 18 | a0001c0002t0002g0004 a0001c0002t0002g0225 a0001c0002t0002g0232 others(15): Show |
18 | HG01192.hp2 HG01243.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.604-834C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980364 | |||||||
| chr11:980390 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-808T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980390 | |||||||
| chr11:980397 | G | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.604-801G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980397 | |||||||
| chr11:980397 | G | CTGCCCGG others(1445): Show |
1 | a0001c0002t0004g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(1452): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980397 | |||||||
| chr11:980397 | G | CTGCCCGG others(1115): Show |
1 | a0001c0002t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.604-802_604-801ins others(1122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980397 | |||||||
| chr11:980397 | G | GTGCCCGG others(1577): Show |
1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.604-776_604-775ins others(1584): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(2171): Show |
1 | a0001c0002t0002g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.604-776_604-775ins others(2178): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(2105): Show |
2 | a0001c0002t0002g0232 a0001c0002t0002g0234 |
2 | HG01346.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.604-776_604-775ins others(2112): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(1775): Show |
1 | a0001c0002t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.604-776_604-775ins others(1782): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(92): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.604-736_604-735ins others(99): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(1049): Show |
1 | a0001c0002t0002g0247 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.604-769_604-768ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(1049): Show |
2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.604-769_604-768ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980397 | G | GTGCCCGG others(1049): Show |
8 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0243 others(5): Show |
8 | HG00597.hp2 HG00621.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.604-769_604-768ins others(1056): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980397 | ||||||
| chr11:980423 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-775T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980423 | |||||||
| chr11:980430 | C | CTGCCCGG others(1511): Show |
1 | a0001c0002t0004g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-743_604-742ins others(1518): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1478): Show |
1 | a0001c0002t0004g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.604-743_604-742ins others(1485): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1412): Show |
1 | a0001c0002t0004g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.604-743_604-742ins others(1419): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1445): Show |
2 | a0001c0002t0002g0225 a0001c0008t0004g0236 |
2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.604-743_604-742ins others(1452): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1412): Show |
1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.604-743_604-742ins others(1419): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1379): Show |
1 | a0001c0002t0004g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.604-743_604-742ins others(1386): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1346): Show |
1 | a0001c0002t0004g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-743_604-742ins others(1353): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(752): Show |
1 | a0001c0002t0004g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.604-743_604-742ins others(759): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(719): Show |
3 | a0001c0002t0004g0228 a0001c0002t0004g0252 a0002c0007t0004g0224 |
3 | HG02622.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.604-743_604-742ins others(726): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | CTGCCCGG others(1115): Show |
1 | a0001c0004t0009g0259 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604-703_604-702ins others(1122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980430 | ||||||
| chr11:980430 | C | G | 5 | a0001c0002t0002g0160 a0001c0002t0004g0222 a0001c0002t0004g0227 others(2): Show |
5 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-768C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980430 | |||||||
| chr11:980430 | C | GTGCCCGG others(1115): Show |
1 | a0001c0002t0002g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.604-769_604-768ins others(1122): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980430 | |||||||
| chr11:980446 | C | CCTGGAGC others(455): Show |
1 | a0001c0001t0002g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.604-736_604-735ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980446 | ||||||
| chr11:980454 | G | GGTGACAG others(455): Show |
1 | a0001c0001t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.604-736_604-735ins others(462): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980454 | ||||||
| chr11:980456 | T | C | 16 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(13): Show |
16 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.604-742T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980456 | |||||||
| chr11:980463 | G | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.604-735G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980463 | |||||||
| chr11:980463 | G | GTGCCCGG others(59): Show |
1 | a0001c0002t0002g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-703_604-702ins others(66): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980463 | ||||||
| chr11:980489 | T | C | 7 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(4): Show |
7 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.604-709T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980489 | |||||||
| chr11:980496 | G | C | 22 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0225 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.604-702G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980496 | |||||||
| chr11:980522 | T | C | 3 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 |
3 | HG01346.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.604-676T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980522 | |||||||
| chr11:980529 | C | G | 1 | a0001c0002t0002g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-669C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980529 | |||||||
| chr11:980564 | G | A | 134 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.604-634G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980564 | |||||||
| chr11:980564 | G | GCCCGGTG others(356): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0116 |
2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.604-626_604-625ins others(363): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr11 | 980564 | ||||||
| chr11:980690 | G | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.604-508G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980690 | |||||||
| chr11:980741 | C | T | 1 | a0001c0013t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.604-457C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980741 | |||||||
| chr11:980860 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.604-338G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980860 | |||||||
| chr11:980989 | C | A | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-209C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 5/21 | chr11 | 980989 | |||||||
| chr11:981420 | C | T | 1 | a0001c0001t0014g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.705+121C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981420 | |||||||
| chr11:981540 | G | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.705+241G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981540 | |||||||
| chr11:981744 | T | G | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+445T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981744 | |||||||
| chr11:981892 | G | A | 1 | a0001c0002t0003g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.705+593G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981892 | |||||||
| chr11:981943 | G | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.705+644G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981943 | |||||||
| chr11:981963 | G | A | 1 | a0001c0002t0004g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705+664G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 981963 | |||||||
| chr11:982090 | G | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.705+791G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982090 | |||||||
| chr11:982291 | T | A | 1 | a0001c0002t0003g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.705+992T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982291 | |||||||
| chr11:982294 | T | A | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.705+995T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982294 | |||||||
| chr11:982350 | C | T | 1 | a0001c0003t0006g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.705+1051C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982350 | |||||||
| chr11:982544 | G | A | 1 | a0001c0002t0002g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.705+1245G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982544 | |||||||
| chr11:982720 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+1421G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982720 | |||||||
| chr11:982732 | T | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.705+1433T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982732 | |||||||
| chr11:982796 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.705+1497C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 982796 | |||||||
| chr11:983017 | CT | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0005g0104 others(48): Show |
51 | HG00544.hp2 HG00597.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.706-1607delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 983017 | ||||||
| chr11:983017 | CTT | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.706-1608_706-1607d others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 983017 | ||||||
| chr11:983025 | T | C | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1620T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983025 | |||||||
| chr11:983040 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.706-1605A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983040 | |||||||
| chr11:983142 | C | T | 3 | a0001c0002t0002g0246 a0001c0002t0002g0250 a0001c0002t0002g0257 |
3 | NA18990.hp2 NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.706-1503C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983142 | |||||||
| chr11:983239 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.706-1406C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983239 | |||||||
| chr11:983315 | G | A | 1 | a0001c0002t0004g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.706-1330G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983315 | |||||||
| chr11:983369 | ATTAT | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.706-1249_706-1246d others(6): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 983369 | ||||||
| chr11:983414 | A | G | 1 | a0001c0003t0002g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.706-1231A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983414 | |||||||
| chr11:983422 | G | C | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.706-1223G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983422 | |||||||
| chr11:983451 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.706-1194T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983451 | |||||||
| chr11:983451 | T | G | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.706-1194T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983451 | |||||||
| chr11:983452 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.706-1193G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983452 | |||||||
| chr11:983460 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.706-1185A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983460 | |||||||
| chr11:983475 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.706-1170T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983475 | |||||||
| chr11:983506 | T | C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0024 others(17): Show |
20 | HG00140.hp2 HG01071.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.706-1139T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983506 | |||||||
| chr11:983529 | C | G | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(90): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.706-1116C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983529 | |||||||
| chr11:983531 | C | G | 1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.706-1114C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983531 | |||||||
| chr11:983531 | C | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1114C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983531 | |||||||
| chr11:983532 | G | A | 1 | a0001c0002t0005g0146 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.706-1113G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983532 | |||||||
| chr11:983539 | T | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0014g0126 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.706-1106T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983539 | |||||||
| chr11:983543 | T | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0014g0126 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.706-1102T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983543 | |||||||
| chr11:983558 | AT | A | 7 | a0001c0001t0003g0130 a0001c0002t0002g0004 a0001c0002t0002g0005 others(4): Show |
7 | HG01433.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-1081delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 983558 | ||||||
| chr11:983561 | T | C | 2 | a0001c0003t0002g0149 a0001c0004t0010g0169 |
2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.706-1084T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983561 | |||||||
| chr11:983573 | T | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0056 others(8): Show |
11 | HG00642.hp1 HG01071.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-1072T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983573 | |||||||
| chr11:983581 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.706-1064C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983581 | |||||||
| chr11:983584 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0002t0002g0133 others(1): Show |
4 | HG01952.hp1 HG02738.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-1061T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983584 | |||||||
| chr11:983590 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0005g0083 a0001c0002t0003g0143 others(2): Show |
5 | HG01081.hp1 HG01258.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1055A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983590 | |||||||
| chr11:983595 | G | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0043 others(9): Show |
12 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-1050G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983595 | |||||||
| chr11:983596 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0043 others(8): Show |
11 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.706-1049G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983596 | |||||||
| chr11:983600 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.706-1045G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983600 | |||||||
| chr11:983601 | T | G | 1 | a0001c0001t0014g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.706-1044T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983601 | |||||||
| chr11:983602 | C | G | 4 | a0001c0002t0002g0241 a0001c0002t0002g0246 a0001c0002t0002g0250 others(1): Show |
4 | HG02027.hp2 NA18990.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1043C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983602 | |||||||
| chr11:983605 | G | A | 1 | a0001c0002t0004g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.706-1040G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983605 | |||||||
| chr11:983605 | G | C | 2 | a0001c0006t0001g0037 a0001c0012t0001g0097 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.706-1040G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983605 | |||||||
| chr11:983607 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.706-1038T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983607 | |||||||
| chr11:983608 | C | A | 1 | a0001c0001t0014g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.706-1037C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983608 | |||||||
| chr11:983618 | T | C | 10 | a0001c0002t0003g0184 a0001c0003t0002g0135 a0001c0003t0002g0162 others(7): Show |
10 | HG02280.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-1027T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983618 | |||||||
| chr11:983625 | C | T | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.706-1020C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983625 | |||||||
| chr11:983630 | G | A | 2 | a0001c0003t0002g0135 a0001c0003t0002g0162 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.706-1015G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983630 | |||||||
| chr11:983641 | T | C | 6 | a0001c0003t0002g0203 a0001c0003t0002g0204 a0001c0003t0002g0211 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-1004T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983641 | |||||||
| chr11:983648 | G | GC | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-996dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 983648 | ||||||
| chr11:983651 | G | A | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-994G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983651 | |||||||
| chr11:983662 | C | T | 6 | a0001c0003t0002g0203 a0001c0003t0002g0204 a0001c0003t0002g0211 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-983C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983662 | |||||||
| chr11:983663 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG02056.hp1 HG02132.hp1 HG03195.hp1 others(10): Show |
intron_variant | MODIFIER | c.706-982G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983663 | |||||||
| chr11:983664 | G | T | 111 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0025 others(108): Show |
111 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.706-981G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983664 | |||||||
| chr11:983672 | C | T | 7 | a0001c0003t0002g0149 a0001c0003t0002g0203 a0001c0003t0002g0204 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-973C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983672 | |||||||
| chr11:983673 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.706-972G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983673 | |||||||
| chr11:983675 | A | G | 4 | a0001c0001t0002g0054 a0001c0002t0002g0241 a0001c0003t0002g0149 others(1): Show |
4 | HG02027.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-970A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983675 | |||||||
| chr11:983678 | T | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.706-967T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983678 | |||||||
| chr11:983694 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.706-951T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983694 | |||||||
| chr11:983712 | T | G | 1 | a0001c0001t0001g0017 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.706-933T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983712 | |||||||
| chr11:983966 | T | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.706-679T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 983966 | |||||||
| chr11:984125 | C | CACTT | 4 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0004t0009g0259 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-519_706-516dup others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 984125 | ||||||
| chr11:984246 | G | T | 1 | a0001c0006t0001g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.706-399G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984246 | |||||||
| chr11:984252 | G | A | 1 | a0001c0002t0003g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.706-393G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984252 | |||||||
| chr11:984421 | C | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0129 others(4): Show |
7 | HG01109.hp1 HG02129.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-224C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984421 | |||||||
| chr11:984530 | A | C | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-115A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984530 | |||||||
| chr11:984605 | G | A | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.706-40G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984605 | |||||||
| chr11:984617 | G | A | 4 | a0001c0005t0003g0132 a0001c0005t0003g0144 a0001c0005t0003g0181 others(1): Show |
4 | HG00621.hp1 HG03704.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-28G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 6/21 | chr11 | 984617 | |||||||
| chr11:984902 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.814+149G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 7/21 | chr11 | 984902 | |||||||
| chr11:985006 | T | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.814+253T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 7/21 | chr11 | 985006 | |||||||
| chr11:985272 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.815-163C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 7/21 | chr11 | 985272 | |||||||
| chr11:985620 | A | G | 1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.962+38A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985620 | |||||||
| chr11:985657 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.962+75C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985657 | |||||||
| chr11:985658 | G | A | 5 | a0001c0003t0002g0203 a0001c0003t0002g0211 a0001c0003t0002g0216 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.962+76G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985658 | |||||||
| chr11:985690 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.962+108T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985690 | |||||||
| chr11:985697 | C | T | 4 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(1): Show |
4 | HG01192.hp2 HG01346.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.962+115C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985697 | |||||||
| chr11:985879 | A | G | 1 | a0001c0004t0002g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.962+297A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985879 | |||||||
| chr11:985880 | G | A | 1 | a0001c0004t0002g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.962+298G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985880 | |||||||
| chr11:985904 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.962+322C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985904 | |||||||
| chr11:985945 | T | C | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+363T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 985945 | |||||||
| chr11:986005 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962+423C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986005 | |||||||
| chr11:986081 | C | T | 5 | a0001c0002t0002g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+499C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986081 | |||||||
| chr11:986105 | TGGGTCTT others(7): Show |
T | 1 | a0001c0001t0001g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.962+527_962+540del others(14): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 986105 | ||||||
| chr11:986114 | C | T | 1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.962+532C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986114 | |||||||
| chr11:986185 | C | A | 147 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.963-600C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986185 | |||||||
| chr11:986221 | T | A | 147 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.963-564T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986221 | |||||||
| chr11:986259 | A | G | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.963-526A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986259 | |||||||
| chr11:986390 | G | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.963-395G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986390 | |||||||
| chr11:986559 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.963-226C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986559 | |||||||
| chr11:986568 | G | C | 3 | a0001c0002t0002g0133 a0001c0002t0002g0158 a0001c0002t0002g0159 |
3 | HG02738.hp1 HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.963-217G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 8/21 | chr11 | 986568 | |||||||
| chr11:987070 | G | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1131+117G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987070 | |||||||
| chr11:987376 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1131+423G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987376 | |||||||
| chr11:987377 | C | T | 1 | a0001c0003t0006g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1131+424C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987377 | |||||||
| chr11:987381 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1131+428G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987381 | |||||||
| chr11:987654 | C | CA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0095 others(7): Show |
10 | HG00642.hp1 HG01952.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1131+716dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 987654 | ||||||
| chr11:987677 | G | A | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1131+724G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987677 | |||||||
| chr11:987885 | C | T | 1 | a0001c0002t0002g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1132-667C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 987885 | |||||||
| chr11:988101 | C | G | 126 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1132-451C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 988101 | |||||||
| chr11:988269 | T | C | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1132-283T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 9/21 | chr11 | 988269 | |||||||
| chr11:988742 | G | A | 1 | a0001c0003t0002g0134 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1269+53G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 988742 | |||||||
| chr11:988771 | C | T | 1 | a0001c0002t0003g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1269+82C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 988771 | |||||||
| chr11:989081 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1269+392G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989081 | |||||||
| chr11:989251 | C | T | 264 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(261): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1269+562C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989251 | |||||||
| chr11:989281 | C | T | 34 | a0001c0002t0002g0001 a0001c0002t0002g0139 a0001c0002t0002g0140 others(31): Show |
34 | HG00544.hp2 HG00597.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1269+592C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989281 | |||||||
| chr11:989320 | C | T | 1 | a0001c0001t0003g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1269+631C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989320 | |||||||
| chr11:989333 | C | CA | 15 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0043 others(12): Show |
15 | HG01109.hp1 HG01192.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1269+657dupA | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 989333 | ||||||
| chr11:989357 | C | T | 2 | a0001c0002t0002g0005 a0001c0005t0003g0181 |
2 | HG02818.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1269+668C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989357 | |||||||
| chr11:989358 | G | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0117 others(4): Show |
7 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1269+669G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989358 | |||||||
| chr11:989815 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1269+1126G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989815 | |||||||
| chr11:989816 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1269+1127T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989816 | |||||||
| chr11:989823 | G | A | 2 | a0001c0002t0002g0232 a0001c0002t0003g0190 |
2 | HG03540.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1269+1134G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989823 | |||||||
| chr11:989844 | C | T | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1269+1155C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989844 | |||||||
| chr11:989915 | G | GT | 8 | a0001c0001t0001g0045 a0001c0002t0002g0005 a0001c0003t0002g0200 others(5): Show |
8 | HG02083.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1269+1234dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 989915 | ||||||
| chr11:989986 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1269+1297G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989986 | |||||||
| chr11:990048 | T | G | 1 | a0001c0002t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1269+1359T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990048 | |||||||
| chr11:990052 | A | G | 1 | a0001c0002t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1269+1363A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990052 | |||||||
| chr11:990053 | G | A | 1 | a0001c0002t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1269+1364G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990053 | |||||||
| chr11:990113 | T | G | 1 | a0001c0003t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1269+1424T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990113 | |||||||
| chr11:990199 | C | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0129 others(5): Show |
8 | HG01109.hp1 HG02523.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1269+1510C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990199 | |||||||
| chr11:990250 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(78): Show |
81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1269+1561C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990250 | |||||||
| chr11:990254 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0121 |
2 | HG00280.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1269+1565C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990254 | |||||||
| chr11:990426 | CGGGAGCC others(21): Show |
C | 2 | a0001c0004t0009g0259 a0001c0004t0009g0260 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1269+1740_1269+176 others(32): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 990426 | ||||||
| chr11:990510 | T | TGAGGTCC others(9): Show |
1 | a0001c0002t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1269+1823_1269+183 others(20): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 990510 | ||||||
| chr11:990557 | C | T | 1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1269+1868C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990557 | |||||||
| chr11:990633 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1270-1870T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990633 | |||||||
| chr11:990657 | G | A | 1 | a0001c0003t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1270-1846G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990657 | |||||||
| chr11:990725 | T | C | 164 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1270-1778T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990725 | |||||||
| chr11:990793 | T | G | 9 | a0001c0002t0001g0071 a0001c0002t0002g0155 a0001c0002t0002g0163 others(6): Show |
9 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270-1710T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990793 | |||||||
| chr11:990812 | T | C | 9 | a0001c0002t0001g0071 a0001c0002t0002g0155 a0001c0002t0002g0163 others(6): Show |
9 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270-1691T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990812 | |||||||
| chr11:990819 | A | G | 4 | a0001c0002t0005g0145 a0001c0002t0005g0146 a0001c0002t0005g0194 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-1684A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990819 | |||||||
| chr11:990850 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1270-1653C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990850 | |||||||
| chr11:990884 | A | C | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1270-1619A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990884 | |||||||
| chr11:990885 | C | A | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1270-1618C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990885 | |||||||
| chr11:990948 | C | T | 1 | a0001c0002t0003g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1270-1555C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 990948 | |||||||
| chr11:991017 | C | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG02056.hp1 HG02132.hp1 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.1270-1486C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991017 | |||||||
| chr11:991099 | G | A | 126 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1270-1404G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991099 | |||||||
| chr11:991103 | A | G | 1 | a0001c0002t0002g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1270-1400A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991103 | |||||||
| chr11:991109 | C | G | 126 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1270-1394C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991109 | |||||||
| chr11:991203 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1270-1300G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991203 | |||||||
| chr11:991252 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1270-1251C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991252 | |||||||
| chr11:991315 | T | C | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1270-1188T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991315 | |||||||
| chr11:991399 | T | C | 1 | a0001c0002t0002g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1270-1104T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991399 | |||||||
| chr11:991492 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0003g0130 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1270-1011G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991492 | |||||||
| chr11:991530 | C | T | 125 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1270-973C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991530 | |||||||
| chr11:991607 | C | A | 264 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(261): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-896C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991607 | |||||||
| chr11:991638 | A | G | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270-865A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991638 | |||||||
| chr11:991686 | G | GGCTCCAG others(10): Show |
1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1270-815_1270-799d others(19): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 991686 | ||||||
| chr11:991708 | T | TG | 10 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0045 others(7): Show |
10 | HG00140.hp1 HG00544.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270-788dupG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 991708 | ||||||
| chr11:991765 | G | A | 1 | a0001c0002t0003g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1270-738G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 991765 | |||||||
| chr11:992015 | G | GAAGGGGA others(4): Show |
1 | a0001c0001t0005g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1270-487_1270-477d others(13): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 992015 | ||||||
| chr11:992098 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1270-405A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 992098 | |||||||
| chr11:992106 | G | A | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1270-397G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 992106 | |||||||
| chr11:992166 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1270-337C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 992166 | |||||||
| chr11:992286 | C | T | 4 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0085 others(1): Show |
4 | HG01258.hp1 HG01358.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-217C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 992286 | |||||||
| chr11:992691 | G | T | 126 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.1452+6G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992691 | |||||||
| chr11:992694 | C | G | 2 | a0001c0002t0004g0228 a0001c0002t0004g0252 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1452+9C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992694 | |||||||
| chr11:992776 | C | A | 2 | a0001c0001t0001g0123 a0001c0001t0003g0130 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1452+91C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992776 | |||||||
| chr11:992800 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1452+115T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992800 | |||||||
| chr11:992824 | T | A | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1452+139T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992824 | |||||||
| chr11:992956 | C | T | 1 | a0002c0007t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1452+271C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992956 | |||||||
| chr11:992980 | C | T | 1 | a0001c0002t0002g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1452+295C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992980 | |||||||
| chr11:992998 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1453-286C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 992998 | |||||||
| chr11:993021 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1453-263C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 993021 | |||||||
| chr11:993034 | TC | T | 3 | a0001c0002t0003g0143 a0001c0002t0003g0176 a0001c0003t0002g0210 |
3 | HG02523.hp2 HG03831.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1453-246delC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 993034 | ||||||
| chr11:993115 | G | A | 4 | a0001c0002t0005g0145 a0001c0002t0005g0146 a0001c0002t0005g0194 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-169G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 993115 | |||||||
| chr11:993219 | C | T | 1 | a0001c0002t0004g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1453-65C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | chr11 | 993219 | |||||||
| chr11:993256 | A | AC | 8 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0068 others(5): Show |
8 | HG00621.hp1 HG01496.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-24dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 993256 | ||||||
| chr11:993449 | G | A | 1 | a0001c0003t0006g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1550+68G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993449 | |||||||
| chr11:993456 | CACCAGCT others(11): Show |
C | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1550+76_1550+93del others(18): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993456 | |||||||
| chr11:993462 | C | G | 6 | a0001c0003t0002g0203 a0001c0003t0002g0204 a0001c0003t0002g0211 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1550+81C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993462 | |||||||
| chr11:993483 | G | A | 1 | a0001c0002t0003g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1550+102G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993483 | |||||||
| chr11:993520 | T | C | 8 | a0001c0001t0006g0009 a0001c0001t0006g0010 a0001c0002t0002g0232 others(5): Show |
8 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1550+139T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993520 | |||||||
| chr11:993679 | T | TC | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
43 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1551-66dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 993679 | ||||||
| chr11:993679 | TC | T | 27 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0052 others(24): Show |
27 | HG00558.hp2 HG01255.hp2 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.1551-66delC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 993679 | ||||||
| chr11:993684 | C | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(16): Show |
19 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1551-70C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993684 | |||||||
| chr11:993694 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1551-60G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993694 | |||||||
| chr11:993742 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1551-12C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993742 | |||||||
| chr11:993745 | C | G | 39 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0042 others(36): Show |
39 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1551-9C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993745 | |||||||
| chr11:993750 | C | G | 2 | a0001c0001t0005g0088 a0001c0002t0002g0159 |
2 | HG01106.hp2 HG04228.hp1 |
splice_region_variant&intron_variant | LOW | c.1551-4C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 12/21 | chr11 | 993750 | |||||||
| chr11:993993 | G | GC | 5 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0001g0123 others(2): Show |
5 | HG01257.hp1 HG02258.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1782+13dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 993993 | ||||||
| chr11:993998 | C | A | 1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1782+13C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/21 | chr11 | 993998 | |||||||
| chr11:994005 | C | A | 1 | a0001c0008t0004g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1782+20C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/21 | chr11 | 994005 | |||||||
| chr11:994049 | T | TC | 3 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0002t0004g0223 |
3 | HG01433.hp1 HG04199.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1783-20dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 994049 | ||||||
| chr11:994320 | G | T | 1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+75G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994320 | |||||||
| chr11:994321 | C | G | 1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+76C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994321 | |||||||
| chr11:994348 | A | T | 1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+103A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994348 | |||||||
| chr11:994397 | G | T | 1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+152G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994397 | |||||||
| chr11:994425 | T | TC | 3 | a0001c0002t0004g0223 a0001c0003t0006g0263 a0001c0005t0003g0144 |
3 | HG00621.hp1 HG01433.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1956+182dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994425 | ||||||
| chr11:994440 | C | G | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1956+195C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994440 | |||||||
| chr11:994479 | G | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1956+234G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994479 | |||||||
| chr11:994497 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1956+252C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994497 | |||||||
| chr11:994538 | G | GC | 7 | a0001c0001t0001g0045 a0001c0001t0001g0079 a0001c0001t0001g0113 others(4): Show |
7 | HG01496.hp1 HG02258.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1956+299dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994538 | ||||||
| chr11:994542 | C | T | 1 | a0001c0001t0013g0064 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1956+297C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994542 | |||||||
| chr11:994629 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1956+384G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994629 | |||||||
| chr11:994743 | G | GC | 7 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0113 others(4): Show |
7 | HG00741.hp2 HG01516.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+504dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994743 | ||||||
| chr11:994760 | C | T | 2 | a0001c0001t0003g0103 a0001c0001t0005g0082 |
2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1956+515C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994760 | |||||||
| chr11:994793 | G | A | 4 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(1): Show |
4 | HG01192.hp2 HG01346.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+548G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994793 | |||||||
| chr11:994797 | G | GTCCCGGG others(240): Show |
1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1956+612_1956+613i others(249): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994797 | ||||||
| chr11:994797 | G | GTCCCGGG others(240): Show |
1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1956+653_1956+654i others(249): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994797 | ||||||
| chr11:994797 | G | GTCCCGGG others(240): Show |
1 | a0001c0001t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1956+643_1956+644i others(249): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994797 | ||||||
| chr11:994798 | T | TC | 3 | a0001c0001t0001g0076 a0001c0001t0001g0115 a0001c0001t0001g0124 |
3 | HG02896.hp2 HG04199.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1956+556dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994798 | ||||||
| chr11:994842 | C | T | 1 | a0001c0005t0003g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1956+597C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994842 | |||||||
| chr11:994842 | CGGGGGCC others(75): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1956+625_1956+706d others(84): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994842 | ||||||
| chr11:994843 | G | A | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1956+598G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994843 | |||||||
| chr11:994907 | G | GC | 9 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0114 others(6): Show |
9 | HG00741.hp1 HG01192.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1956+668dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994907 | ||||||
| chr11:994924 | T | C | 40 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1956+679T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994924 | |||||||
| chr11:994948 | A | AC | 4 | a0001c0001t0001g0117 a0001c0001t0005g0084 a0001c0002t0003g0003 others(1): Show |
4 | HG01192.hp1 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+707dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994948 | ||||||
| chr11:994952 | C | CCGCTGTC others(240): Show |
1 | a0001c0001t0019g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1956+707_1956+708i others(249): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994952 | |||||||
| chr11:994952 | C | CGCTGTCC others(240): Show |
1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1956+711_1956+712i others(249): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994952 | ||||||
| chr11:994952 | C | CGCTGTCC others(239): Show |
12 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0003g0130 others(9): Show |
12 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1956+711_1956+712i others(248): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994952 | ||||||
| chr11:994952 | C | CGCTGTCC others(245): Show |
1 | a0001c0001t0007g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1956+711_1956+712i others(254): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 994952 | ||||||
| chr11:994952 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 |
3 | HG01261.hp2 HG01516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1956+707C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994952 | |||||||
| chr11:994957 | G | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1956+712G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994957 | |||||||
| chr11:994959 | T | C | 20 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1956+714T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994959 | |||||||
| chr11:994961 | G | CTCCCGGG others(239): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1956+715_1956+716i others(248): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994961 | |||||||
| chr11:994965 | C | G | 1 | a0003c0009t0003g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1956+720C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994965 | |||||||
| chr11:994970 | G | C | 1 | a0003c0009t0003g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1956+725G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994970 | |||||||
| chr11:994977 | T | C | 1 | a0001c0005t0003g0192 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1956+732T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994977 | |||||||
| chr11:994991 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0005 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1956+746C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994991 | |||||||
| chr11:994994 | T | C | 20 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1956+749T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 994994 | |||||||
| chr11:995018 | T | TC | 3 | a0001c0001t0001g0122 a0001c0001t0003g0103 a0001c0002t0002g0244 |
3 | HG04204.hp2 NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1956+776dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995018 | ||||||
| chr11:995030 | A | AC | 7 | a0001c0002t0002g0004 a0001c0002t0003g0176 a0001c0003t0002g0210 others(4): Show |
7 | HG00621.hp1 HG02055.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+789dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995030 | ||||||
| chr11:995086 | G | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0058 others(5): Show |
8 | HG00642.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1956+841G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995086 | |||||||
| chr11:995090 | G | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0105 others(19): Show |
22 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1956+845G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995090 | |||||||
| chr11:995134 | T | C | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1956+889T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995134 | |||||||
| chr11:995153 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1956+908C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995153 | |||||||
| chr11:995303 | A | T | 1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+1058A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995303 | |||||||
| chr11:995314 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
6 | NA18950.hp1 NA18950.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1956+1069G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995314 | |||||||
| chr11:995357 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1956+1112A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995357 | |||||||
| chr11:995611 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1956+1366T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995611 | |||||||
| chr11:995635 | C | T | 33 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1956+1390C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995635 | |||||||
| chr11:995658 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1956+1413T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995658 | |||||||
| chr11:995693 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1956+1448T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995693 | |||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0004c0014t0001g0261 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1956+1462_1956+146 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1326): Show |
1 | a0001c0001t0007g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1337): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1313): Show |
1 | a0001c0001t0003g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0002t0003g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1313): Show |
1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1315): Show |
1 | a0001c0001t0001g0115 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1326): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1308): Show |
1 | a0001c0001t0001g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1319): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1291): Show |
1 | a0001c0004t0009g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1302): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1309): Show |
1 | a0001c0001t0001g0035 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1320): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1309): Show |
1 | a0001c0002t0002g0247 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1320): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0003c0009t0003g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0002t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1318): Show |
1 | a0001c0001t0001g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1329): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0002t0003g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1322): Show |
1 | a0001c0002t0002g0164 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1333): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1305): Show |
1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1316): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1309): Show |
1 | a0001c0002t0003g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1320): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0002t0005g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1307): Show |
1 | a0001c0001t0005g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1318): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1292): Show |
1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1303): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1303): Show |
2 | a0001c0002t0002g0005 a0001c0004t0010g0169 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1314): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1313): Show |
1 | a0001c0004t0002g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0003t0002g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1313): Show |
1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0001t0001g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0005c0011t0002g0242 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1335): Show |
1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1346): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1306): Show |
1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1317): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1283): Show |
5 | a0001c0001t0002g0054 a0001c0002t0002g0001 a0001c0002t0002g0139 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1294): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1298): Show |
12 | a0001c0002t0002g0213 a0001c0003t0002g0134 a0001c0003t0002g0136 others(9): Show |
12 | HG00544.hp2 HG00597.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1309): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
6 | NA18950.hp1 NA18950.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
2 | a0001c0001t0001g0108 a0001c0002t0003g0003 |
2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0005t0003g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0001t0017g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0001t0005g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
10 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0005g0020 others(7): Show |
10 | HG01106.hp2 HG01258.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1287): Show |
1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1298): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1305): Show |
1 | a0001c0002t0002g0244 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1316): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0002t0003g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0001t0002g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0003t0002g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
2 | a0001c0003t0002g0135 a0001c0003t0002g0162 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0002t0002g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1311): Show |
1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1322): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1309): Show |
1 | a0001c0001t0005g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1320): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1313): Show |
1 | a0001c0003t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1274): Show |
1 | a0001c0002t0004g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1285): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1317): Show |
13 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0129 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1328): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1299): Show |
2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1310): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1297): Show |
1 | a0002c0007t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1308): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1315): Show |
1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1326): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1274): Show |
1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1285): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1273): Show |
9 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0226 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1956+1470_1956+147 others(1284): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1272): Show |
1 | a0001c0002t0004g0228 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1283): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1272): Show |
1 | a0001c0002t0004g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1283): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1274): Show |
1 | a0001c0002t0002g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1285): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1275): Show |
1 | a0001c0002t0002g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1286): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1274): Show |
1 | a0001c0002t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1285): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1272): Show |
1 | a0001c0002t0002g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1283): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1310): Show |
1 | a0001c0001t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1321): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1293): Show |
1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1304): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1328): Show |
1 | a0001c0002t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1339): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1291): Show |
1 | a0001c0003t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1302): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1305): Show |
1 | a0001c0001t0005g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1316): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1307): Show |
1 | a0001c0002t0003g0002 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1318): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1312): Show |
1 | a0001c0001t0001g0122 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1323): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1293): Show |
1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1304): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1308): Show |
1 | a0001c0001t0001g0022 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1319): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1264): Show |
1 | a0001c0008t0004g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1275): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1302): Show |
1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1313): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1296): Show |
1 | a0001c0004t0009g0259 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1307): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1297): Show |
1 | a0001c0002t0011g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1308): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1301): Show |
1 | a0001c0003t0006g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1312): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGCTGAG others(1351): Show |
1 | a0001c0001t0001g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1362): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995698 | A | AGGGCTGA others(1320): Show |
1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1956+1455_1956+145 others(1331): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995698 | ||||||
| chr11:995699 | G | GGCTGAGC others(1303): Show |
1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1314): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995699 | ||||||
| chr11:995710 | A | ACATCTTG others(1313): Show |
1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1956+1470_1956+147 others(1324): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995710 | ||||||
| chr11:995785 | C | T | 20 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1956+1540C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995785 | |||||||
| chr11:995789 | T | TC | 6 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0001g0121 others(3): Show |
6 | HG00280.hp1 HG01109.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1956+1550dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995789 | ||||||
| chr11:995823 | A | G | 1 | a0001c0003t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1956+1578A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995823 | |||||||
| chr11:995840 | A | C | 40 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1956+1595A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995840 | |||||||
| chr11:995906 | TTTCTCCC others(12): Show |
T | 1 | a0001c0001t0005g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1956+1665_1956+168 others(23): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995906 | ||||||
| chr11:995918 | T | TG | 3 | a0001c0001t0001g0048 a0001c0004t0009g0260 a0004c0014t0001g0261 |
3 | HG01255.hp2 NA18994.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1956+1676dupG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 995918 | ||||||
| chr11:995996 | G | A | 1 | a0001c0002t0004g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1956+1751G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 995996 | |||||||
| chr11:996165 | C | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1956+1920C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996165 | |||||||
| chr11:996211 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1956+1966C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996211 | |||||||
| chr11:996213 | C | T | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1956+1968C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996213 | |||||||
| chr11:996291 | G | A | 2 | a0001c0002t0004g0222 a0001c0002t0004g0227 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1956+2046G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996291 | |||||||
| chr11:996486 | T | C | 20 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1956+2241T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996486 | |||||||
| chr11:996522 | C | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1956+2277C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996522 | |||||||
| chr11:996588 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1956+2343G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996588 | |||||||
| chr11:996624 | TG | T | 3 | a0001c0001t0001g0061 a0001c0001t0003g0103 a0001c0002t0003g0176 |
3 | HG04204.hp2 NA18968.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1956+2382delG | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 996624 | ||||||
| chr11:996815 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1956+2570C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996815 | |||||||
| chr11:996867 | G | GTCCTGAC others(28): Show |
40 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0123 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1956+2649_1956+265 others(39): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 996867 | ||||||
| chr11:996946 | G | A | 7 | a0001c0001t0005g0104 a0001c0003t0006g0138 a0001c0003t0006g0263 others(4): Show |
7 | HG01358.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1956+2701G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 996946 | |||||||
| chr11:997019 | G | T | 1 | a0001c0002t0002g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1956+2774G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997019 | |||||||
| chr11:997269 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1956+3024C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997269 | |||||||
| chr11:997340 | C | G | 7 | a0001c0002t0004g0226 a0001c0002t0004g0228 a0001c0002t0004g0235 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-3092C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997340 | |||||||
| chr11:997434 | C | T | 20 | a0001c0001t0002g0054 a0001c0002t0002g0001 a0001c0002t0002g0139 others(17): Show |
20 | HG00544.hp2 HG00597.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-2998C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997434 | |||||||
| chr11:997503 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1957-2929A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997503 | |||||||
| chr11:997540 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1957-2892A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997540 | |||||||
| chr11:997587 | C | CTTTCCTA others(8): Show |
1 | a0001c0001t0001g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1957-2844_1957-283 others(19): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 997587 | ||||||
| chr11:997658 | G | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(262): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1957-2774G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997658 | |||||||
| chr11:997733 | C | T | 76 | a0001c0001t0002g0054 a0001c0001t0003g0041 a0001c0002t0002g0001 others(73): Show |
76 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1957-2699C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997733 | |||||||
| chr11:997836 | C | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1957-2596C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997836 | |||||||
| chr11:998100 | C | G | 1 | a0001c0002t0002g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1957-2332C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998100 | |||||||
| chr11:998192 | C | G | 1 | a0001c0001t0013g0064 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1957-2240C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998192 | |||||||
| chr11:998199 | A | AC | 3 | a0001c0001t0001g0115 a0001c0001t0005g0082 a0001c0002t0003g0184 |
3 | HG01261.hp1 NA18939.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1957-2231dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998199 | ||||||
| chr11:998255 | C | T | 1 | a0001c0003t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1957-2177C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998255 | |||||||
| chr11:998306 | T | TCCCCATT others(15): Show |
1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1957-2113_1957-209 others(26): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998306 | ||||||
| chr11:998322 | C | CACCCGCC others(9): Show |
1 | a0001c0001t0001g0026 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1957-2105_1957-209 others(20): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998322 | ||||||
| chr11:998323 | A | ACCCGCCC others(12): Show |
62 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0027 others(59): Show |
62 | HG00423.hp1 HG00597.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.1957-2090_1957-207 others(23): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998323 | ||||||
| chr11:998323 | A | ACCCGCCC others(31): Show |
1 | a0001c0003t0002g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1957-2072_1957-207 others(42): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998323 | ||||||
| chr11:998340 | C | CCCCCCGC others(11): Show |
1 | a0001c0001t0001g0078 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1957-2089_1957-207 others(22): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998340 | ||||||
| chr11:998347 | C | CCCCCATT others(11): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0111 |
2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1957-2072_1957-207 others(22): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 998347 | ||||||
| chr11:998553 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1957-1879G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998553 | |||||||
| chr11:998835 | A | G | 1 | a0001c0002t0002g0239 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1957-1597A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998835 | |||||||
| chr11:998839 | G | A | 13 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(10): Show |
13 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1957-1593G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998839 | |||||||
| chr11:998852 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0050 others(3): Show |
6 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-1580C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998852 | |||||||
| chr11:998949 | C | G | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1957-1483C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998949 | |||||||
| chr11:999118 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1314T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999118 | |||||||
| chr11:999121 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1311T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999121 | |||||||
| chr11:999127 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1305G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999127 | |||||||
| chr11:999129 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1303T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999129 | |||||||
| chr11:999136 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1296G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999136 | |||||||
| chr11:999138 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1294G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999138 | |||||||
| chr11:999142 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1290A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999142 | |||||||
| chr11:999146 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1286G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999146 | |||||||
| chr11:999147 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1285A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999147 | |||||||
| chr11:999151 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1281A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999151 | |||||||
| chr11:999152 | C | T | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-1280C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999152 | |||||||
| chr11:999158 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1274T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999158 | |||||||
| chr11:999159 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1273G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999159 | |||||||
| chr11:999161 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1271T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999161 | |||||||
| chr11:999163 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1269C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999163 | |||||||
| chr11:999165 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1267T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999165 | |||||||
| chr11:999166 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1266G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999166 | |||||||
| chr11:999178 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1254G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999178 | |||||||
| chr11:999180 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1252G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999180 | |||||||
| chr11:999186 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1246A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999186 | |||||||
| chr11:999188 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1244T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999188 | |||||||
| chr11:999190 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1242A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999190 | |||||||
| chr11:999193 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1239A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999193 | |||||||
| chr11:999196 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1236T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999196 | |||||||
| chr11:999199 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1233T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999199 | |||||||
| chr11:999203 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1229C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999203 | |||||||
| chr11:999204 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1228G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999204 | |||||||
| chr11:999204 | G | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1957-1228G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999204 | |||||||
| chr11:999210 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1222T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999210 | |||||||
| chr11:999211 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1221C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999211 | |||||||
| chr11:999212 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1220C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999212 | |||||||
| chr11:999214 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1218T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999214 | |||||||
| chr11:999215 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1217G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999215 | |||||||
| chr11:999217 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1215G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999217 | |||||||
| chr11:999221 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1211T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999221 | |||||||
| chr11:999222 | TGCCCCAG others(4): Show |
T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1209_1957-119 others(15): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999222 | |||||||
| chr11:999243 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1189T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999243 | |||||||
| chr11:999244 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1188T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999244 | |||||||
| chr11:999247 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1185T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999247 | |||||||
| chr11:999248 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1184G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999248 | |||||||
| chr11:999249 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1183G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999249 | |||||||
| chr11:999250 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1182G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999250 | |||||||
| chr11:999254 | G | C | 1 | a0001c0003t0004g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1957-1178G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999254 | |||||||
| chr11:999254 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1178G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999254 | |||||||
| chr11:999257 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1175T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999257 | |||||||
| chr11:999258 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1174G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999258 | |||||||
| chr11:999268 | A | ACACTGTA others(12): Show |
1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1164_1957-116 others(23): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999268 | |||||||
| chr11:999273 | A | G | 1 | a0001c0004t0009g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1957-1159A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999273 | |||||||
| chr11:999282 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1150T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999282 | |||||||
| chr11:999284 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1148A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999284 | |||||||
| chr11:999286 | C | T | 3 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0007g0092 |
3 | HG00280.hp2 HG01496.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1957-1146C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999286 | |||||||
| chr11:999296 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1957-1136G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999296 | |||||||
| chr11:999372 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1957-1060C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999372 | |||||||
| chr11:999373 | G | A | 1 | a0001c0002t0004g0222 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1957-1059G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999373 | |||||||
| chr11:999380 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1957-1052C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999380 | |||||||
| chr11:999426 | C | T | 1 | a0001c0003t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1957-1006C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999426 | |||||||
| chr11:999620 | T | C | 140 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1957-812T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999620 | |||||||
| chr11:999622 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1957-810C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999622 | |||||||
| chr11:999675 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0058 others(5): Show |
8 | HG00642.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1957-757G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999675 | |||||||
| chr11:999764 | T | C | 13 | a0001c0001t0003g0103 a0001c0001t0005g0020 a0001c0001t0005g0082 others(10): Show |
13 | HG01106.hp2 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1957-668T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999764 | |||||||
| chr11:999796 | G | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1957-636G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999796 | |||||||
| chr11:999803 | C | CT | 13 | a0001c0001t0003g0103 a0001c0001t0005g0020 a0001c0001t0005g0082 others(10): Show |
13 | HG01106.hp2 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1957-611dupT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 999803 | ||||||
| chr11:999803 | CT | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1957-611delT | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 999803 | ||||||
| chr11:999803 | CTT | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0048 others(6): Show |
9 | HG00741.hp1 HG01069.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1957-612_1957-611d others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 999803 | ||||||
| chr11:999804 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0063 |
2 | HG00423.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1957-628T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999804 | |||||||
| chr11:999889 | C | T | 1 | a0001c0003t0002g0215 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1957-543C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999889 | |||||||
| chr11:999928 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0098 |
2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1957-504C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 999928 | |||||||
| chr11:1000044 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1957-388G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 1000044 | |||||||
| chr11:1000131 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1957-301T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 1000131 | |||||||
| chr11:1000217 | A | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1957-215A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 1000217 | |||||||
| chr11:1000357 | G | A | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1957-75G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 1000357 | |||||||
| chr11:1000364 | C | T | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1957-68C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 1000364 | |||||||
| chr11:1000731 | C | T | 19 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(16): Show |
19 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2123+133C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000731 | |||||||
| chr11:1000854 | G | A | 1 | a0001c0001t0007g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2123+256G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000854 | |||||||
| chr11:1000878 | C | T | 2 | a0001c0002t0004g0226 a0001c0002t0004g0254 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2123+280C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000878 | |||||||
| chr11:1000935 | G | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2123+337G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000935 | |||||||
| chr11:1000954 | C | T | 1 | a0001c0002t0002g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2123+356C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000954 | |||||||
| chr11:1001383 | C | T | 1 | a0001c0006t0018g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2123+785C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001383 | |||||||
| chr11:1001415 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2123+817C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001415 | |||||||
| chr11:1001416 | G | A | 9 | a0001c0001t0003g0041 a0001c0002t0003g0002 a0001c0002t0003g0003 others(6): Show |
9 | HG00423.hp2 HG00558.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.2123+818G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001416 | |||||||
| chr11:1001557 | T | G | 2 | a0001c0002t0004g0228 a0001c0002t0004g0252 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2123+959T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001557 | |||||||
| chr11:1001561 | G | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2123+963G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001561 | |||||||
| chr11:1001607 | G | A | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2123+1009G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001607 | |||||||
| chr11:1001623 | G | T | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2123+1025G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001623 | |||||||
| chr11:1001748 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2123+1150C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001748 | |||||||
| chr11:1001760 | G | T | 1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2123+1162G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001760 | |||||||
| chr11:1001774 | G | A | 9 | a0001c0001t0003g0041 a0001c0002t0003g0002 a0001c0002t0003g0003 others(6): Show |
9 | HG00423.hp2 HG00558.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.2123+1176G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001774 | |||||||
| chr11:1001883 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0087 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2123+1285T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001883 | |||||||
| chr11:1001985 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2123+1387C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001985 | |||||||
| chr11:1002054 | G | T | 1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2123+1456G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002054 | |||||||
| chr11:1002215 | C | G | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2124-1507C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002215 | |||||||
| chr11:1002236 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0094 |
2 | HG00140.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2124-1486C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002236 | |||||||
| chr11:1002242 | G | A | 1 | a0001c0001t0015g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2124-1480G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002242 | |||||||
| chr11:1002308 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2124-1414C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002308 | |||||||
| chr11:1002398 | C | A | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2124-1324C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002398 | |||||||
| chr11:1002399 | T | G | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2124-1323T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002399 | |||||||
| chr11:1002420 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2124-1302G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002420 | |||||||
| chr11:1002534 | G | T | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2124-1188G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002534 | |||||||
| chr11:1002735 | C | T | 1 | a0001c0003t0002g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2124-987C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002735 | |||||||
| chr11:1002926 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2124-796C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1002926 | |||||||
| chr11:1002991 | G | GC | 4 | a0001c0001t0005g0082 a0001c0002t0002g0241 a0001c0002t0002g0247 others(1): Show |
4 | HG01261.hp1 HG02027.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.2124-727dupC | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 1002991 | ||||||
| chr11:1003077 | T | A | 1 | a0001c0002t0003g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2124-645T>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1003077 | |||||||
| chr11:1003343 | C | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2124-379C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1003343 | |||||||
| chr11:1003523 | G | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.2124-199G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1003523 | |||||||
| chr11:1003642 | G | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.2124-80G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1003642 | |||||||
| chr11:1003879 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2206+75A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1003879 | |||||||
| chr11:1004053 | A | G | 1 | a0001c0002t0003g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2206+249A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1004053 | |||||||
| chr11:1004276 | T | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2206+472T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1004276 | |||||||
| chr11:1004432 | C | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2206+628C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1004432 | |||||||
| chr11:1004700 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2206+896C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1004700 | |||||||
| chr11:1004932 | G | A | 264 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(261): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2206+1128G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1004932 | |||||||
| chr11:1005108 | A | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2206+1304A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005108 | |||||||
| chr11:1005139 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2206+1335G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005139 | |||||||
| chr11:1005160 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2206+1356C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005160 | |||||||
| chr11:1005205 | A | T | 1 | a0001c0001t0017g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2207-1323A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005205 | |||||||
| chr11:1005297 | T | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2207-1231T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005297 | |||||||
| chr11:1005305 | G | C | 1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2207-1223G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005305 | |||||||
| chr11:1005308 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2207-1220C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005308 | |||||||
| chr11:1005697 | G | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2207-831G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005697 | |||||||
| chr11:1005808 | G | A | 15 | a0001c0002t0002g0225 a0001c0002t0004g0222 a0001c0002t0004g0223 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2207-720G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1005808 | |||||||
| chr11:1006048 | G | A | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2207-480G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006048 | |||||||
| chr11:1006050 | G | A | 1 | a0001c0002t0002g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2207-478G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006050 | |||||||
| chr11:1006226 | C | T | 1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2207-302C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006226 | |||||||
| chr11:1006230 | G | A | 2 | a0001c0002t0002g0139 a0001c0002t0002g0140 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2207-298G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006230 | |||||||
| chr11:1006256 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0047 others(6): Show |
9 | HG00642.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2207-272C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006256 | |||||||
| chr11:1006258 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2207-270C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006258 | |||||||
| chr11:1006329 | T | G | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2207-199T>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006329 | |||||||
| chr11:1006330 | A | C | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2207-198A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006330 | |||||||
| chr11:1006332 | C | G | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2207-196C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006332 | |||||||
| chr11:1006333 | C | G | 1 | a0001c0002t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2207-195C>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006333 | |||||||
| chr11:1006338 | C | T | 20 | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2207-190C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006338 | |||||||
| chr11:1006344 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2207-184A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006344 | |||||||
| chr11:1006345 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2207-183C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 16/21 | chr11 | 1006345 | |||||||
| chr11:1006970 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2296+353G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1006970 | |||||||
| chr11:1007021 | C | T | 1 | a0001c0002t0004g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2296+404C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007021 | |||||||
| chr11:1007165 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0105 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2296+548C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007165 | |||||||
| chr11:1007421 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2297-591G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007421 | |||||||
| chr11:1007436 | C | T | 3 | a0001c0002t0004g0228 a0001c0002t0004g0252 a0001c0002t0004g0253 |
3 | HG02717.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2297-576C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007436 | |||||||
| chr11:1007738 | C | A | 1 | a0001c0002t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2297-274C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007738 | |||||||
| chr11:1007831 | T | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2297-181T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007831 | |||||||
| chr11:1007848 | G | A | 6 | a0001c0003t0006g0138 a0001c0003t0006g0263 a0001c0003t0006g0264 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2297-164G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007848 | |||||||
| chr11:1007958 | C | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2297-54C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1007958 | |||||||
| chr11:1008008 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.2297-4G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 17/21 | chr11 | 1008008 | |||||||
| chr11:1008144 | C | T | 1 | a0001c0004t0010g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2420+9C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008144 | |||||||
| chr11:1008157 | C | T | 1 | a0001c0006t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2420+22C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008157 | |||||||
| chr11:1008177 | C | T | 2 | a0001c0004t0002g0195 a0001c0004t0002g0196 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2420+42C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008177 | |||||||
| chr11:1008398 | GCC | G | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420+265_2420+266d others(4): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 1008398 | ||||||
| chr11:1008468 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0125 |
2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.2420+333T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008468 | |||||||
| chr11:1008472 | GGGTGCAG others(6): Show |
G | 1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420+341_2420+353d others(15): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 1008472 | ||||||
| chr11:1008664 | G | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2421-436G>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008664 | |||||||
| chr11:1008756 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2421-344A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1008756 | |||||||
| chr11:1009035 | C | A | 1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2421-65C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 18/21 | chr11 | 1009035 | |||||||
| chr11:1009307 | C | T | 12 | a0001c0001t0005g0020 a0001c0001t0005g0082 a0001c0001t0005g0083 others(9): Show |
12 | HG01106.hp2 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2538-21C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 19/21 | chr11 | 1009307 | |||||||
| chr11:1009416 | C | T | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(93): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.2607+19C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009416 | |||||||
| chr11:1009427 | GACACGCA others(43): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2607+42_2607+91del others(50): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009427 | ||||||
| chr11:1009431 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2607+34C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009431 | |||||||
| chr11:1009435 | G | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG01192.hp2 HG01346.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2607+38G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009435 | |||||||
| chr11:1009439 | GTGACCCC others(43): Show |
G | 1 | a0001c0005t0003g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2607+80_2607+129de others(51): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009439 | ||||||
| chr11:1009477 | A | AACACGCA others(43): Show |
1 | a0001c0001t0001g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2607+92_2607+141du others(51): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009477 | ||||||
| chr11:1009477 | A | G | 6 | a0001c0001t0001g0047 a0001c0003t0002g0134 a0001c0003t0002g0136 others(3): Show |
6 | HG02572.hp1 NA18944.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.2607+80A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009477 | |||||||
| chr11:1009489 | A | G | 5 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0197 others(2): Show |
5 | NA18944.hp2 NA18945.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2607+92A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009489 | |||||||
| chr11:1009490 | T | C | 5 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0197 others(2): Show |
5 | NA18944.hp2 NA18945.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2607+93T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009490 | |||||||
| chr11:1009496 | C | A | 1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2607+99C>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009496 | |||||||
| chr11:1009496 | C | AGCGCCAG others(143): Show |
4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0197 others(1): Show |
4 | NA18944.hp2 NA18945.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2607+98_2607+99ins others(150): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009496 | |||||||
| chr11:1009496 | C | CGCGCCAG others(143): Show |
1 | a0001c0002t0002g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2608-95_2608-94ins others(150): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009496 | ||||||
| chr11:1009515 | A | ACGGCCCC others(93): Show |
1 | a0001c0001t0005g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2607+137_2608-50du others(101): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009515 | ||||||
| chr11:1009515 | A | ACGGCCCC others(93): Show |
1 | a0001c0002t0003g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2608-100_2608-99in others(101): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009515 | ||||||
| chr11:1009515 | A | ACGGCCCC others(93): Show |
19 | a0001c0001t0002g0054 a0001c0002t0002g0001 a0001c0002t0002g0139 others(16): Show |
19 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2608-100_2608-99in others(101): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009515 | ||||||
| chr11:1009515 | A | ACGGCCCC others(143): Show |
2 | a0001c0003t0002g0207 a0001c0003t0002g0221 |
2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2608-100_2608-99in others(151): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009515 | ||||||
| chr11:1009515 | A | ACGGCCCC others(193): Show |
1 | a0001c0002t0003g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2608-100_2608-99in others(201): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009515 | ||||||
| chr11:1009515 | A | G | 5 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0197 others(2): Show |
5 | NA18944.hp2 NA18945.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2607+118A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009515 | |||||||
| chr11:1009516 | C | CGGCCCCG others(144): Show |
1 | a0001c0003t0002g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2607+136_2607+137i others(153): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009516 | ||||||
| chr11:1009539 | G | GCGACCCA others(143): Show |
1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2608-100_2608-99in others(151): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009539 | ||||||
| chr11:1009539 | GCGACCCA others(43): Show |
G | 7 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0053 others(4): Show |
7 | HG01243.hp2 HG01978.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2608-99_2608-50del others(50): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr11 | 1009539 | ||||||
| chr11:1009584 | A | T | 7 | a0001c0003t0002g0198 a0001c0003t0002g0203 a0001c0003t0002g0204 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2608-99A>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009584 | |||||||
| chr11:1009589 | A | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2608-94A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009589 | |||||||
| chr11:1009591 | G | A | 1 | a0001c0002t0005g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2608-92G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009591 | |||||||
| chr11:1009596 | A | C | 7 | a0001c0003t0002g0198 a0001c0003t0002g0203 a0001c0003t0002g0204 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2608-87A>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009596 | |||||||
| chr11:1009597 | G | A | 6 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0244 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2608-86G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009597 | |||||||
| chr11:1009599 | G | A | 15 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0124 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.2608-84G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009599 | |||||||
| chr11:1009622 | C | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2608-61C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009622 | |||||||
| chr11:1009641 | G | A | 15 | a0001c0002t0004g0222 a0001c0002t0004g0223 a0001c0002t0004g0226 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2608-42G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 20/21 | chr11 | 1009641 | |||||||
| chr11:1009890 | T | C | 125 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2742+73T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 21/21 | chr11 | 1009890 | |||||||
| chr11:1010112 | C | T | 4 | a0001c0002t0002g0241 a0001c0002t0002g0246 a0001c0002t0002g0250 others(1): Show |
4 | HG02027.hp2 NA18990.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.2742+295C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 21/21 | chr11 | 1010112 | |||||||
| chr11:1010199 | C | T | 1 | a0001c0003t0002g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2743-349C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 21/21 | chr11 | 1010199 | |||||||
| chr11:1010408 | C | T | 1 | a0001c0006t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2743-140C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 21/21 | chr11 | 1010408 | |||||||
| chr11:1010421 | C | T | 5 | a0001c0003t0002g0203 a0001c0003t0002g0211 a0001c0003t0002g0216 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2743-127C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 21/21 | chr11 | 1010421 |