Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 939 | 264 | 69 | 52 | 98 | 12 | 31 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0002 | 0/0 | 939 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0003 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0004 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0005 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2820 | 120 | 22 | 30 | 46 | 9 | 13 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0002 | 1/1 | 2820 | 89 | 23 | 18 | 32 | 2 | 12 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0003 | 0/0 | 2820 | 37 | 18 | 1 | 15 | 0 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0004 | 0/0 | 2820 | 5 | 4 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0005 | 0/0 | 2820 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0006 | 0/0 | 2820 | 4 | 1 | 0 | 1 | 1 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0007 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0008 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0009 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0010 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0011 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0012 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0013 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0014 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| c0015 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1768 | 100 | 19 | 21 | 44 | 7 | 9 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0002 | 1/1 | 1768 | 74 | 23 | 12 | 29 | 1 | 7 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0003 | 0/0 | 1768 | 38 | 0 | 4 | 21 | 0 | 13 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0004 | 0/0 | 1768 | 16 | 12 | 4 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0005 | 0/0 | 1768 | 12 | 5 | 6 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0006 | 0/0 | 1768 | 8 | 8 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0007 | 0/0 | 1768 | 6 | 0 | 2 | 0 | 3 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0008 | 0/0 | 1768 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0009 | 0/0 | 1768 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0010 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0011 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0012 | 0/0 | 1768 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0013 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0014 | 0/0 | 1768 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0015 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0016 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0017 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0018 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| t0019 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 120 | 22 | 30 | 46 | 9 | 13 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002 | a0001 | c0002 | 1/1 | 89 | 23 | 18 | 32 | 2 | 12 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 37 | 18 | 1 | 15 | 0 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 4 | 1 | 0 | 1 | 1 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0002c0009 | a0002 | c0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0004c0014 | a0004 | c0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0005c0011 | a0005 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 93 | 19 | 19 | 42 | 6 | 7 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 8 | 1 | 6 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 6 | 0 | 2 | 0 | 3 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 1/1 | 41 | 9 | 11 | 15 | 1 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 29 | 0 | 4 | 16 | 0 | 9 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0004 | a0001 | c0002 | t0004 | 0/0 | 13 | 11 | 2 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0011 | a0001 | c0002 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0002t0012 | a0001 | c0002 | t0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 28 | 12 | 0 | 13 | 0 | 3 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0003t0006 | a0001 | c0003 | t0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0003t0008 | a0001 | c0003 | t0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0004t0009 | a0001 | c0004 | t0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0004t0010 | a0001 | c0004 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0005t0003 | a0001 | c0005 | t0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0006t0018 | a0001 | c0006 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0008t0004 | a0001 | c0008 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0010t0005 | a0001 | c0010 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0001c0015t0003 | a0001 | c0015 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0002c0009t0003 | a0002 | c0009 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0003c0007t0004 | a0003 | c0007 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0004c0014t0001 | a0004 | c0014 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| a0005c0011t0002 | a0005 | c0011 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0003g0040 | a0001 | c0001 | t0003 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0003g0102 | a0001 | c0001 | t0003 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0003g0129 | a0001 | c0001 | t0003 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0019 | a0001 | c0001 | t0005 | g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0081 | a0001 | c0001 | t0005 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0082 | a0001 | c0001 | t0005 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0083 | a0001 | c0001 | t0005 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0084 | a0001 | c0001 | t0005 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0087 | a0001 | c0001 | t0005 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0103 | a0001 | c0001 | t0005 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0005g0152 | a0001 | c0001 | t0005 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0006g0008 | a0001 | c0001 | t0006 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0006g0009 | a0001 | c0001 | t0006 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0039 | a0001 | c0001 | t0007 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0088 | a0001 | c0001 | t0007 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0089 | a0001 | c0001 | t0007 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0090 | a0001 | c0001 | t0007 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0091 | a0001 | c0001 | t0007 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0007g0105 | a0001 | c0001 | t0007 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0013g0063 | a0001 | c0001 | t0013 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0014g0125 | a0001 | c0001 | t0014 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0015g0066 | a0001 | c0001 | t0015 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0016g0045 | a0001 | c0001 | t0016 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0017g0069 | a0001 | c0001 | t0017 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0001t0019g0020 | a0001 | c0001 | t0019 | g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0001g0071 | a0001 | c0002 | t0001 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0003 | a0001 | c0002 | t0002 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0004 | a0001 | c0002 | t0002 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0132 | a0001 | c0002 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0136 | a0001 | c0002 | t0002 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0143 | a0001 | c0002 | t0002 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0146 | a0001 | c0002 | t0002 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0151 | a0001 | c0002 | t0002 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0153 | a0001 | c0002 | t0002 | g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0154 | a0001 | c0002 | t0002 | g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0155 | a0001 | c0002 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0156 | a0001 | c0002 | t0002 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0159 | a0001 | c0002 | t0002 | g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0160 | a0001 | c0002 | t0002 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0161 | a0001 | c0002 | t0002 | g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0162 | a0001 | c0002 | t0002 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0163 | a0001 | c0002 | t0002 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0167 | a0001 | c0002 | t0002 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0168 | a0001 | c0002 | t0002 | g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0204 | a0001 | c0002 | t0002 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0209 | a0001 | c0002 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0217 | a0001 | c0002 | t0002 | g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0219 | a0001 | c0002 | t0002 | g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0221 | a0001 | c0002 | t0002 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0226 | a0001 | c0002 | t0002 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0233 | a0001 | c0002 | t0002 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0234 | a0001 | c0002 | t0002 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0235 | a0001 | c0002 | t0002 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0240 | a0001 | c0002 | t0002 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0241 | a0001 | c0002 | t0002 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0242 | a0001 | c0002 | t0002 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0244 | a0001 | c0002 | t0002 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0245 | a0001 | c0002 | t0002 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0246 | a0001 | c0002 | t0002 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0247 | a0001 | c0002 | t0002 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0248 | a0001 | c0002 | t0002 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0249 | a0001 | c0002 | t0002 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0250 | a0001 | c0002 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0251 | a0001 | c0002 | t0002 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0252 | a0001 | c0002 | t0002 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0257 | a0001 | c0002 | t0002 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0002g0258 | a0001 | c0002 | t0002 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0001 | a0001 | c0002 | t0003 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0002 | a0001 | c0002 | t0003 | g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0137 | a0001 | c0002 | t0003 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0138 | a0001 | c0002 | t0003 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0139 | a0001 | c0002 | t0003 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0147 | a0001 | c0002 | t0003 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0148 | a0001 | c0002 | t0003 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0149 | a0001 | c0002 | t0003 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0169 | a0001 | c0002 | t0003 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0171 | a0001 | c0002 | t0003 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0172 | a0001 | c0002 | t0003 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0173 | a0001 | c0002 | t0003 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0174 | a0001 | c0002 | t0003 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0175 | a0001 | c0002 | t0003 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0176 | a0001 | c0002 | t0003 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0178 | a0001 | c0002 | t0003 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0179 | a0001 | c0002 | t0003 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0180 | a0001 | c0002 | t0003 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0181 | a0001 | c0002 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0182 | a0001 | c0002 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0183 | a0001 | c0002 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0184 | a0001 | c0002 | t0003 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0186 | a0001 | c0002 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0187 | a0001 | c0002 | t0003 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0197 | a0001 | c0002 | t0003 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0198 | a0001 | c0002 | t0003 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0201 | a0001 | c0002 | t0003 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0202 | a0001 | c0002 | t0003 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0003g0239 | a0001 | c0002 | t0003 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0166 | a0001 | c0002 | t0004 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0223 | a0001 | c0002 | t0004 | g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0224 | a0001 | c0002 | t0004 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0227 | a0001 | c0002 | t0004 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0228 | a0001 | c0002 | t0004 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0229 | a0001 | c0002 | t0004 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0230 | a0001 | c0002 | t0004 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0231 | a0001 | c0002 | t0004 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0232 | a0001 | c0002 | t0004 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0236 | a0001 | c0002 | t0004 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0253 | a0001 | c0002 | t0004 | g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0254 | a0001 | c0002 | t0004 | g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0004g0255 | a0001 | c0002 | t0004 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0005g0141 | a0001 | c0002 | t0005 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0005g0142 | a0001 | c0002 | t0005 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0005g0190 | a0001 | c0002 | t0005 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0011g0164 | a0001 | c0002 | t0011 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0002t0012g0220 | a0001 | c0002 | t0012 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0005 | a0001 | c0003 | t0002 | g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0133 | a0001 | c0003 | t0002 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0134 | a0001 | c0003 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0145 | a0001 | c0003 | t0002 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0157 | a0001 | c0003 | t0002 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0158 | a0001 | c0003 | t0002 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0193 | a0001 | c0003 | t0002 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0194 | a0001 | c0003 | t0002 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0195 | a0001 | c0003 | t0002 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0196 | a0001 | c0003 | t0002 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0199 | a0001 | c0003 | t0002 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0200 | a0001 | c0003 | t0002 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0203 | a0001 | c0003 | t0002 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0205 | a0001 | c0003 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0206 | a0001 | c0003 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0207 | a0001 | c0003 | t0002 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0208 | a0001 | c0003 | t0002 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0210 | a0001 | c0003 | t0002 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0211 | a0001 | c0003 | t0002 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0212 | a0001 | c0003 | t0002 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0213 | a0001 | c0003 | t0002 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0214 | a0001 | c0003 | t0002 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0215 | a0001 | c0003 | t0002 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0216 | a0001 | c0003 | t0002 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0218 | a0001 | c0003 | t0002 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0222 | a0001 | c0003 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0238 | a0001 | c0003 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0002g0259 | a0001 | c0003 | t0002 | g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0004g0256 | a0001 | c0003 | t0004 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0135 | a0001 | c0003 | t0006 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0264 | a0001 | c0003 | t0006 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0265 | a0001 | c0003 | t0006 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0266 | a0001 | c0003 | t0006 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0267 | a0001 | c0003 | t0006 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0006g0268 | a0001 | c0003 | t0006 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0008g0185 | a0001 | c0003 | t0008 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0003t0008g0189 | a0001 | c0003 | t0008 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0004t0002g0191 | a0001 | c0004 | t0002 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0004t0002g0192 | a0001 | c0004 | t0002 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0004t0009g0260 | a0001 | c0004 | t0009 | g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0004t0009g0261 | a0001 | c0004 | t0009 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0004t0010g0165 | a0001 | c0004 | t0010 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0005t0003g0131 | a0001 | c0005 | t0003 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0005t0003g0140 | a0001 | c0005 | t0003 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0005t0003g0177 | a0001 | c0005 | t0003 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0005t0003g0188 | a0001 | c0005 | t0003 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0006t0001g0036 | a0001 | c0006 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0006t0001g0043 | a0001 | c0006 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0006t0001g0126 | a0001 | c0006 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0006t0018g0099 | a0001 | c0006 | t0018 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0008t0004g0237 | a0001 | c0008 | t0004 | g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0010t0005g0144 | a0001 | c0010 | t0005 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0012t0001g0096 | a0001 | c0012 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0013t0001g0127 | a0001 | c0013 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0001c0015t0003g0170 | a0001 | c0015 | t0003 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0002c0009t0003g0150 | a0002 | c0009 | t0003 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0003c0007t0004g0225 | a0003 | c0007 | t0004 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0004c0014t0001g0262 | a0004 | c0014 | t0001 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| a0005c0011t0002g0243 | a0005 | c0011 | t0002 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A2_chr11_920870_1017240 | AP2A2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0090 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0105 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0222 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00609 | hp1 | a0001 | c0015 | t0003 | g0170 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00621 | hp1 | a0001 | c0005 | t0003 | g0140 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00673 | hp2 | a0001 | c0006 | t0001 | g0043 | EAS | CHS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00738 | hp1 | a0001 | c0001 | t0019 | g0020 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0148 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0187 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0087 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01109 | hp1 | a0001 | c0013 | t0001 | g0127 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0223 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01243 | hp1 | a0001 | c0008 | t0004 | g0237 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01243 | hp2 | a0001 | c0004 | t0009 | g0260 | AMR | PUR | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0161 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0089 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0168 | EUR | IBS | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0228 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0151 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01943 | hp1 | a0001 | c0003 | t0004 | g0256 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0162 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0159 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01981 | hp1 | a0001 | c0001 | t0016 | g0045 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0141 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02056 | hp2 | a0001 | c0003 | t0008 | g0185 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02135 | hp2 | a0001 | c0003 | t0008 | g0189 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | CDX | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02257 | hp1 | a0001 | c0004 | t0010 | g0165 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0190 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0213 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02280 | hp2 | a0001 | c0003 | t0006 | g0266 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0236 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0200 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0206 | EAS | KHV | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0133 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0232 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02615 | hp2 | a0001 | c0006 | t0018 | g0099 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02622 | hp1 | a0003 | c0007 | t0004 | g0225 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02630 | hp1 | a0001 | c0003 | t0006 | g0135 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02698 | hp1 | a0002 | c0009 | t0003 | g0150 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0149 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0229 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0199 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0005 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0255 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0207 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0208 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0154 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0214 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0253 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0227 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0176 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0264 | AFR | ESN | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0145 | AFR | GWD | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0254 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03654 | hp1 | a0001 | c0006 | t0001 | g0036 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0088 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03704 | hp1 | a0001 | c0005 | t0003 | g0131 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0083 | SAS | PJL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0259 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0186 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0138 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0238 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0179 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04199 | hp1 | a0001 | c0012 | t0001 | g0096 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0147 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0155 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0125 | SAS | STU | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0157 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18522 | hp2 | a0001 | c0010 | t0005 | g0144 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | CHB | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18747 | hp2 | a0001 | c0001 | t0015 | g0066 | EAS | CHB | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18939 | hp2 | a0001 | c0002 | t0011 | g0164 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0203 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18994 | hp1 | a0004 | c0014 | t0001 | g0262 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0218 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19004 | hp2 | a0001 | c0005 | t0003 | g0188 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19005 | hp1 | a0001 | c0005 | t0003 | g0177 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0063 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0194 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0265 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0166 | AFR | LWK | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0205 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19082 | hp1 | a0005 | c0011 | t0002 | g0243 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0210 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0069 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19240 | hp1 | a0001 | c0004 | t0009 | g0261 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0191 | AFR | YRI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0226 | AFR | ASW | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0268 | AFR | ASW | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20752 | hp1 | a0001 | c0006 | t0001 | g0126 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20805 | hp1 | a0001 | c0002 | t0012 | g0220 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0091 | EUR | TSI | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | GIH | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0230 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0212 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0192 | AFR | ACB | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0158 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 |
| NA20300 | hp2 | a0001 | c0003 | t0006 | g0267 | AFR | USA | AP2A2_chr11_920870_1017240 | AP2A2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0217 | REF | REF | AP2A2_chr11_920870_1017240 | AP2A2 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0153 | REF | REF | AP2A2_chr11_920870_1017240 | AP2A2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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 | a0002 | 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 | a0003 | 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 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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 | a0001c0001a0001c0006a0001c0012others(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 | a0001c0012a0001c0013 | 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 | a0001c0003a0001c0006a0001c0013others(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 | a0003c0007 | 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 |
| 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_pos_length | cds_pos_length | 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 | a0001c0001t0003a0001c0002t0003a0001c0003t0008others(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 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(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 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(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 | a0001c0001t0005a0001c0002t0005a0001c0010t0005 | 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 | a0001c0002t0004a0001c0003t0004a0001c0008t0004others(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 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(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 | a0001c0001t0007a0001c0001t0019 | 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 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:926103
|
C | A | 2 | a0001c0002t0003g0001a0001c0002t0003g0002 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0003t0002g0005 | 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 | a0001c0003t0006g0264a0001c0003t0006g0265a0001c0003t0006g0266others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0115others(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 | a0001c0005t0003g0131 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0222 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0114a0001c0002t0002g0204a0001c0002t0002g0209others(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 | |||||
| chr11:927510
|
TAA | T | 6 | a0001c0002t0002g0217a0001c0002t0002g0219a0001c0002t0002g0221others(3): Show | 6 | HG01071.hp2 HG06807.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+1438_67+1439del others(2): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 927510 | |||||
| chr11:927553
|
A | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0012 | 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 | a0001c0002t0004g0223 | 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 | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): 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 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0003t0002g0215 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0010t0005g0144 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0005t0003g0131 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0008t0004g0237 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0004t0009g0260 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0029 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016a0001c0001t0001g0023 | 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 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0137others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0006t0001g0036 | 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 | a0001c0002t0002g0168 | 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 | a0001c0002t0004g0236 | 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 | a0001c0002t0003g0001 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0024others(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 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0124others(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 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0226others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0012t0001g0096 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0003g0187 | 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 | a0001c0002t0002g0136a0001c0002t0002g0221 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0003t0002g0211 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0037 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0094 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0033a0001c0001t0001g0093 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0130 | 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 | a0001c0002t0002g0143 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0011g0164 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0003t0002g0196a0001c0003t0006g0135a0001c0003t0006g0264others(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 | a0001c0001t0001g0113a0001c0005t0003g0131 | 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 | a0001c0001t0001g0116 | 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 | a0001c0003t0002g0196 | 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 | a0001c0002t0011g0164 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0151 | 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 | a0001c0002t0002g0003 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0252 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0252 | 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 | a0001c0002t0002g0132a0001c0002t0002g0155a0001c0002t0002g0156others(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 | a0001c0004t0010g0165 | 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 | a0001c0002t0002g0003a0001c0004t0009g0261 | 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 |
13 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0221others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG02165.hp2 others(10): 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 | a0001c0002t0002g0204a0001c0002t0002g0219a0001c0002t0003g0202others(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 | a0001c0002t0002g0209a0001c0002t0002g0247a0001c0003t0002g0196others(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 | a0001c0003t0002g0195a0001c0003t0002g0210 | 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 | a0001c0003t0006g0265 | 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 | a0001c0003t0002g0157 | 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 | a0001c0002t0003g0137a0001c0002t0003g0138a0001c0002t0003g0147others(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 | a0001c0002t0003g0002a0001c0002t0003g0139a0001c0002t0003g0149others(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 | a0001c0002t0003g0183 | 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 | a0001c0002t0003g0001 | 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 | a0001c0002t0003g0184 | 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 | a0001c0003t0006g0266a0001c0003t0008g0185 | 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 | a0001c0002t0002g0240a0001c0002t0002g0248a0001c0003t0008g0189others(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 | a0001c0002t0002g0241a0001c0002t0002g0244a0001c0002t0002g0246others(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 | a0001c0002t0002g0249a0001c0005t0003g0140 | 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 | a0001c0002t0002g0242 | 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 | a0001c0002t0002g0258a0001c0004t0002g0192 | 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 | a0001c0001t0001g0122a0001c0002t0002g0250a0001c0003t0006g0267others(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 | a0001c0002t0002g0167a0001c0002t0002g0245a0001c0002t0002g0252others(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 | a0001c0002t0002g0159a0001c0002t0002g0160a0001c0002t0002g0161others(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 | a0001c0002t0002g0162a0001c0002t0002g0163 | 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 | a0001c0001t0003g0129a0001c0002t0011g0164 | 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 | a0001c0001t0001g0021a0001c0001t0001g0121a0001c0001t0006g0009others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | |||||
| chr11:935779
|
A | G | 1 | a0001c0002t0002g0217 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67+9691A>G | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 1/21 | chr11 | 935779 | ||||||
| chr11:935794
|
C | T | 7 | a0001c0001t0007g0039a0001c0001t0007g0088a0001c0001t0007g0089others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0038a0001c0001t0003g0129a0001c0002t0002g0003others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0002t0011g0164 | 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 | a0001c0002t0003g0178a0001c0003t0002g0133a0001c0003t0002g0157others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0002t0004g0224 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0236 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0021a0001c0001t0001g0122a0001c0001t0002g0098others(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 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0001t0001g0092a0001c0001t0006g0008a0001c0001t0006g0009others(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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0137others(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 | a0001c0002t0003g0184 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0158 | 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 | a0001c0001t0003g0040 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0116 | 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 | a0001c0002t0003g0184 | 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 | a0001c0001t0001g0033 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0155 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0002t0002g0156a0001c0002t0004g0166 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0095a0001c0001t0001g0122a0001c0001t0001g0123others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0156a0001c0002t0004g0166 | 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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0041a0001c0001t0001g0107a0001c0001t0001g0116others(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 | a0001c0002t0002g0226a0001c0002t0002g0257a0001c0002t0004g0223others(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 | a0001c0001t0001g0094 | 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 | a0001c0004t0010g0165 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0005g0087 | 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 | a0001c0005t0003g0140 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0033a0001c0001t0001g0093 | 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 | a0001c0003t0002g0203 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0004g0236 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104 | 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 | a0001c0003t0002g0216 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0155 | 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 | a0001c0001t0001g0010 | 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 | a0001c0002t0002g0258 | 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 | a0001c0001t0001g0124 | 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 | a0001c0002t0003g0201 | 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 | a0001c0001t0003g0102a0001c0001t0005g0081a0001c0001t0005g0082others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | 28 | a0001c0001t0007g0105a0001c0002t0002g0136a0001c0002t0002g0204others(25): Show | 28 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(25): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0005g0019 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0042 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0246 | 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 | a0001c0002t0004g0231 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0003g0102a0001c0001t0005g0081 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0005g0019 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0005g0152 | 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 | a0001c0002t0003g0186 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0032 | 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 | a0001c0002t0002g0151 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0193 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0146 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0003t0002g0206 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0003c0007t0004g0225 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0003g0179 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0005 | 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 | a0001c0001t0001g0046a0001c0002t0004g0236a0001c0002t0004g0255 | 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 | a0001c0001t0001g0011a0001c0001t0001g0080a0001c0001t0001g0086others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0044a0001c0001t0001g0107a0001c0001t0016g0045 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | 125 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(122): Show | 125 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(122): 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0003t0004g0256 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0013 | 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 | a0001c0002t0003g0179 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0146 | 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 | a0001c0002t0003g0172 | 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 | a0001c0001t0014g0125a0001c0002t0004g0231 | 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 | a0001c0001t0005g0152 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0006t0001g0126a0001c0013t0001g0127 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0230 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0010t0005g0144 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0111others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0115 | 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 | a0001c0002t0005g0141a0001c0002t0005g0142a0001c0002t0005g0190others(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 | a0001c0003t0002g0208 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0114 | 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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0004t0009g0261 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0215 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0014g0125 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0006t0001g0036 | 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 | a0001c0002t0002g0162 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0133a0001c0003t0002g0157a0001c0003t0002g0158 | 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 | a0001c0001t0001g0120 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0003a0001c0002t0002g0132a0001c0002t0002g0233others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0240a0001c0003t0002g0238 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0034others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0146 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0002g0053 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0244others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0010g0165 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0124 | 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 | a0001c0002t0002g0151a0001c0002t0002g0156a0001c0002t0002g0159others(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 | a0001c0001t0007g0105 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0051 | 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 | a0001c0002t0003g0137a0001c0002t0003g0138a0001c0002t0003g0139others(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 | a0001c0001t0007g0091 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0003t0002g0193a0001c0003t0002g0203a0001c0003t0002g0205others(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 | a0001c0001t0003g0040 | 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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0004g0232 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0003g0174 | 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 | a0001c0001t0001g0054 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0016a0001c0001t0001g0023 | 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 | a0001c0001t0007g0091 | 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 | a0001c0001t0007g0091 | 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 | a0001c0002t0002g0204a0001c0002t0002g0209a0001c0003t0002g0134others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0005g0087 | 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 | a0001c0003t0006g0135 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0210 | 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 | a0001c0002t0004g0223a0001c0002t0004g0228a0001c0002t0004g0230others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0001t0001g0123 | 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 | a0001c0002t0003g0179 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0010 | 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 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0137others(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 | a0001c0001t0007g0105a0001c0003t0002g0259 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0124 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0055a0001c0001t0001g0056 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0008g0185 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0005t0003g0140 | 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 | a0001c0002t0002g0143a0001c0002t0005g0142 | 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 | a0001c0001t0001g0114 | 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 | a0001c0003t0002g0158a0001c0004t0010g0165 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0143 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0050 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | ||||||
| chr11:964344
|
G | A | 1 | a0001c0002t0002g0217 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.136+4839G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | chr11 | 964344 | ||||||
| chr11:964476
|
A | G | 152 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0211a0001c0003t0002g0218 | 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 | a0001c0002t0002g0246 | 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 | a0001c0006t0018g0099 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0093 | 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 | a0001c0006t0001g0036 | 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 | a0001c0012t0001g0096 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0033 | 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 | a0001c0002t0004g0236 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0032a0001c0006t0001g0043 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0035a0001c0001t0001g0121 | 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 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0050others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0016g0045 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0060a0001c0001t0001g0117a0001c0001t0001g0118others(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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0005g0142 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0003g0129 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0014g0125 | 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 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0006t0001g0126others(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 | a0001c0001t0001g0130 | 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 | a0001c0002t0002g0004 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0204 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0002t0002g0146 | 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 | a0001c0003t0002g0157 | 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 | a0001c0003t0002g0158 | 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 | a0001c0003t0002g0133 | 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 | a0001c0002t0003g0174 | 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 | a0001c0002t0003g0179 | 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 | a0001c0005t0003g0177 | 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 | a0001c0002t0003g0202 | 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 | a0001c0002t0003g0138a0001c0002t0003g0148a0001c0002t0003g0197others(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 | a0001c0002t0003g0137a0001c0002t0003g0149a0001c0002t0003g0172others(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 | a0001c0002t0003g0169a0001c0002t0003g0171a0001c0002t0003g0173others(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 | a0001c0002t0003g0147a0001c0015t0003g0170 | 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 | a0001c0002t0004g0166 | 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 | a0001c0002t0002g0240 | 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 | a0001c0002t0003g0183 | 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 | a0001c0010t0005g0144 | 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 | a0001c0002t0002g0143 | 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 | a0001c0003t0002g0211a0001c0003t0002g0218 | 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 | a0001c0003t0002g0214 | 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 | a0001c0003t0002g0193a0001c0003t0002g0205 | 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 | a0001c0003t0002g0207a0001c0003t0002g0212a0001c0003t0002g0213 | 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 | a0001c0003t0002g0199 | 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 | a0001c0003t0002g0200 | 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 | a0001c0003t0002g0194 | 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 | a0001c0002t0002g0156 | 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 | a0001c0002t0002g0247a0001c0002t0002g0251 | 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 | a0001c0002t0002g0132 | 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 | a0001c0002t0002g0154 | 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 | a0001c0002t0002g0151 | 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 | a0001c0002t0002g0241 | 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 | a0001c0002t0002g0248 | 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 | a0001c0002t0002g0159 | 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 | a0001c0002t0002g0168 | 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 | a0001c0002t0002g0250 | 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 | a0001c0002t0002g0162 | 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 | a0001c0002t0002g0163a0001c0002t0002g0249 | 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 | a0005c0011t0002g0243 | 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 | a0001c0002t0003g0182 | 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 | a0001c0003t0002g0259 | 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 | a0001c0002t0002g0242 | 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 | a0001c0002t0002g0160a0001c0002t0002g0161 | 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 | a0001c0002t0002g0246 | 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 | a0001c0002t0003g0176a0001c0002t0003g0187 | 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 | a0001c0002t0003g0186 | 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 | a0001c0005t0003g0131 | 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 | a0001c0002t0002g0244 | 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 | a0001c0002t0011g0164 | 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 | a0001c0003t0002g0238 | 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 | a0001c0003t0006g0268 | 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 | a0001c0003t0006g0266 | 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 | a0001c0003t0006g0264a0001c0003t0006g0267 | 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 | a0001c0002t0005g0190 | 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 | a0001c0003t0006g0265 | 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 | a0001c0003t0002g0005 | 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 | a0001c0002t0005g0141 | 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 | a0001c0002t0002g0155 | 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 | a0001c0004t0010g0165 | 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 | a0001c0002t0003g0139 | 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 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0005t0003g0140 | 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 | a0001c0002t0002g0258 | 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 | a0001c0001t0005g0152 | 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 | a0001c0003t0008g0185 | 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 | a0001c0003t0002g0145 | 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 | a0001c0003t0008g0189 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0167 | 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 | a0001c0001t0001g0026a0001c0001t0002g0053 | 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 |
5 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0219others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(2): 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 | a0001c0002t0002g0209a0001c0003t0002g0134a0001c0003t0002g0195others(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 | a0001c0003t0006g0135 | 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 | a0001c0002t0002g0245 | 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 | a0001c0002t0002g0252 | 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 | a0001c0004t0009g0261 | 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 | a0001c0004t0009g0260 | 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 | a0001c0001t0001g0035a0001c0001t0001g0121 | 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 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0130others(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 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0006t0018g0099 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0085a0001c0001t0001g0104 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0244a0001c0002t0002g0248a0005c0011t0002g0243 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0003c0007t0004g0225 | 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 | a0001c0002t0004g0229a0001c0002t0004g0253 | 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 | a0001c0002t0004g0227a0001c0002t0004g0254a0001c0002t0004g0255 | 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 | a0001c0001t0002g0053 | 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 | a0001c0002t0002g0204a0001c0003t0002g0193a0001c0003t0002g0194others(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 | a0001c0003t0002g0206 | 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 | a0001c0003t0002g0210 | 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 |
1 | a0001c0002t0002g0217 | 1 | homoSapiens_chm13v2.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(4821): Show |
4 | a0001c0002t0002g0136a0001c0002t0002g0219a0001c0002t0002g0221others(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 | a0001c0003t0002g0215 | 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 | a0001c0003t0002g0208 | 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 | a0001c0002t0002g0209a0001c0003t0002g0134a0001c0003t0002g0195 | 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 | a0001c0003t0002g0216 | 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 | a0001c0003t0002g0196 | 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 | a0001c0003t0002g0203 | 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 | a0001c0003t0002g0222 | 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0001g0108 | 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 | a0001c0006t0018g0099 | 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 | a0001c0001t0001g0077a0001c0001t0001g0079 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0021a0001c0001t0001g0022 | 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 | a0001c0002t0004g0224 | 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 | a0001c0001t0001g0100 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0005g0152a0001c0002t0002g0132a0001c0002t0002g0154others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0075others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0093 | 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 | a0001c0001t0001g0017a0001c0001t0001g0054a0001c0002t0001g0071 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0113 | 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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0004g0223a0001c0002t0004g0224a0001c0002t0004g0228others(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 | a0001c0001t0003g0102a0001c0001t0005g0081a0001c0001t0005g0082others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0136a0001c0002t0002g0219a0001c0002t0002g0221others(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 | a0001c0002t0002g0163 | 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 | a0001c0002t0002g0204a0001c0002t0002g0209a0001c0003t0002g0134others(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 | a0001c0002t0003g0137a0001c0002t0003g0138a0001c0002t0003g0139others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | 148 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(145): Show | 148 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(145): 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 | a0001c0001t0001g0130 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0003g0174 | 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 | 5 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0219others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(2): 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0027others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0061a0001c0002t0002g0226a0001c0002t0002g0233others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0151a0001c0002t0002g0159a0001c0002t0002g0160others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0229a0001c0002t0004g0253 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0002g0191 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0010t0005g0144 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0006t0018g0099 | 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 | a0001c0001t0005g0152a0001c0002t0002g0132a0001c0002t0002g0154others(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 | a0001c0001t0005g0152a0001c0002t0002g0132a0001c0002t0002g0154others(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 | a0001c0002t0003g0137a0001c0002t0003g0138a0001c0002t0003g0139others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0208 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0050 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | 5 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0219others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(2): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0077a0001c0001t0001g0079 | 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 | a0001c0001t0005g0081 | 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 | a0001c0003t0002g0215 | 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 | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): 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 | a0001c0003t0002g0134 | 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 | a0001c0002t0002g0162 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0004 | 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 | a0001c0002t0004g0254 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0003t0006g0135 | 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 | a0001c0002t0003g0179 | 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 | a0001c0002t0002g0249 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0093a0001c0001t0001g0110a0001c0001t0001g0111others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0003g0197a0001c0002t0003g0198a0001c0002t0003g0201others(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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0002t0005g0141 | 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 | a0001c0001t0007g0039 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0003t0002g0145 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235 | 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 | a0001c0002t0004g0227a0001c0002t0004g0229a0001c0002t0004g0236others(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 | a0001c0002t0002g0226a0001c0002t0004g0228a0001c0002t0004g0230others(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 | a0001c0002t0004g0223a0001c0002t0004g0224 | 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 | a0001c0002t0002g0257 | 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 | a0001c0003t0004g0256 | 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 | a0001c0003t0002g0259 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0006t0018g0099 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0007g0090 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0029a0001c0001t0001g0106 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(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 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0042others(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 | a0001c0001t0001g0010a0001c0001t0001g0086 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0116others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0010a0001c0001t0001g0031 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | ||||||
| chr11:975634
|
C | T | 1 | a0001c0002t0002g0217 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.474-1461C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | chr11 | 975634 | ||||||
| chr11:975669
|
C | G | 2 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0199a0001c0003t0002g0207a0001c0003t0002g0212others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0251 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0145 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0003t0002g0157 | 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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0085 | 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 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0245others(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 | a0001c0001t0001g0119 | 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 | a0001c0002t0002g0242a0001c0002t0002g0258 | 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 | a0001c0006t0018g0099 | 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 | 5 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0219others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG06807.hp2 others(2): 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0019g0020 | 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 | a0001c0001t0001g0116 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0038 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0157 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0003 | 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 | a0001c0003t0002g0005a0001c0003t0002g0206a0001c0003t0002g0215 | 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 | a0001c0003t0002g0259 | 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 | a0001c0003t0002g0193a0001c0003t0002g0210 | 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 |
4 | a0001c0002t0002g0136a0001c0002t0002g0217a0001c0002t0002g0219others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG06807.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(1082): Show |
1 | a0001c0002t0012g0220 | 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 | a0001c0002t0002g0209a0001c0003t0002g0134a0001c0003t0002g0195others(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 | a0001c0002t0002g0004 | 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 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0137others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0006t0018g0099 | 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 | a0001c0002t0002g0154 | 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 | a0001c0001t0005g0152 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142 | 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 | a0001c0002t0005g0190 | 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 | a0001c0003t0006g0266 | 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 | a0001c0003t0006g0267 | 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 | a0001c0002t0002g0167 | 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 | a0001c0002t0002g0163 | 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 | a0001c0003t0002g0145 | 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 | a0001c0002t0004g0224 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0004t0009g0261 | 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 | a0001c0004t0010g0165 | 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 | a0001c0010t0005g0144 | 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 | a0001c0003t0002g0205 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0003t0002g0157 | 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 | a0001c0003t0006g0135 | 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 | a0001c0002t0004g0166 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0012t0001g0096 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0002t0002g0242a0001c0002t0002g0247a0001c0002t0002g0251others(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 | a0001c0003t0002g0238 | 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 | a0001c0002t0011g0164 | 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 | a0001c0002t0002g0168 | 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 | a0001c0002t0001g0071a0001c0002t0002g0151a0001c0002t0002g0159others(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 | a0001c0003t0002g0133 | 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 | a0001c0002t0002g0146a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0003t0002g0158 | 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 | a0001c0002t0002g0252 | 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 | a0001c0003t0002g0208 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0057 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0023a0001c0001t0001g0080 | 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 | a0001c0001t0016g0045 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0022others(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 | a0001c0001t0001g0061a0001c0001t0005g0087a0001c0001t0015g0066 | 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 | a0001c0003t0002g0211a0001c0003t0002g0218 | 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 | a0001c0002t0002g0204 | 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 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0207others(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 | a0001c0003t0002g0216 | 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 | a0001c0003t0002g0203a0001c0003t0002g0222 | 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 | a0001c0003t0002g0194 | 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 | 16 | a0001c0002t0002g0136a0001c0002t0002g0209a0001c0002t0002g0217others(13): Show | 16 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(13): 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0006t0001g0036 | 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 | a0001c0001t0007g0088a0001c0001t0007g0105a0001c0001t0019g0020 | 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 | a0001c0001t0001g0119a0001c0001t0007g0089a0001c0001t0007g0090others(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 | a0001c0001t0007g0039 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0004g0223a0001c0002t0004g0228 | 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 | a0001c0001t0001g0112 | 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 | a0001c0002t0002g0003a0001c0002t0002g0226a0001c0002t0002g0233others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0255 | 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 | a0001c0002t0002g0155 | 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 | a0001c0003t0004g0256 | 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 | a0001c0002t0002g0234a0001c0002t0002g0235 | 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 | a0001c0002t0002g0257 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0002t0002g0248 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0244others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0004g0227 | 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 | a0001c0002t0004g0236 | 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 | a0001c0002t0004g0231 | 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 | a0001c0002t0002g0226a0001c0008t0004g0237 | 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 | a0001c0002t0004g0224 | 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 | a0001c0002t0004g0232 | 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 | a0001c0002t0004g0230 | 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 | a0001c0002t0004g0254 | 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 | a0001c0002t0004g0229a0001c0002t0004g0253a0003c0007t0004g0225 | 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 | a0001c0004t0009g0260 | 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 | a0001c0002t0002g0156a0001c0002t0004g0223a0001c0002t0004g0228others(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 | a0001c0002t0002g0132 | 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 | a0001c0001t0002g0098 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0156 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0226others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235 | 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 | a0001c0002t0002g0156 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0058a0001c0001t0001g0115 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0013t0001g0127 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0014g0125 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0003g0147 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0002t0004g0166 | 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 | a0001c0004t0010g0165 | 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 | a0001c0002t0003g0182 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0006g0266 | 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 | a0001c0002t0002g0167 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0005g0103others(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 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0002t0002g0247a0001c0002t0002g0251a0001c0002t0002g0258 | 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 | a0001c0001t0001g0075 | 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 | a0001c0002t0004g0166 | 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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): 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 | a0001c0003t0002g0005 | 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0001g0023 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0023others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0005g0142 | 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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0014g0125others(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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0014g0125others(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 | a0001c0001t0003g0129a0001c0002t0002g0003a0001c0002t0002g0004others(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 | a0001c0003t0002g0145a0001c0004t0010g0165 | 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 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0056others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0054a0001c0001t0001g0080a0001c0002t0002g0132others(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 | a0001c0001t0001g0059a0001c0001t0005g0082a0001c0002t0003g0139others(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 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0042others(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 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0042others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0014g0125 | 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 | a0001c0002t0002g0242a0001c0002t0002g0247a0001c0002t0002g0251others(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 | a0001c0002t0004g0230 | 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 | a0001c0006t0001g0036a0001c0012t0001g0096 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0014g0125 | 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 | a0001c0002t0003g0180a0001c0003t0002g0133a0001c0003t0002g0158others(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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0003t0002g0133a0001c0003t0002g0158 | 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 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0207others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0207others(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 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(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 | 112 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0024others(109): Show | 112 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(109): 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 | a0001c0003t0002g0145a0001c0003t0002g0199a0001c0003t0002g0200others(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 | a0001c0001t0002g0053 | 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 | a0001c0001t0002g0053a0001c0002t0002g0242a0001c0003t0002g0145others(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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0004t0009g0260others(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 | a0001c0006t0001g0043 | 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 | a0001c0002t0003g0148 | 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 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0003t0004g0256 | 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 | a0001c0005t0003g0131a0001c0005t0003g0140a0001c0005t0003g0177others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0002t0011g0164 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0003t0002g0199a0001c0003t0002g0207a0001c0003t0002g0212others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0004t0002g0192 | 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 | a0001c0004t0002g0192 | 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 | a0001c0001t0001g0065 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0143a0001c0002t0005g0141a0001c0002t0005g0142others(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 | a0001c0001t0001g0027 | 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 | a0001c0006t0018g0099 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0002t0002g0132a0001c0002t0002g0154a0001c0002t0002g0155 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0044 | 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 | a0001c0003t0006g0266 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0094others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0154 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0003t0002g0216 | 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 | a0001c0002t0003g0173 | 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 | a0001c0002t0002g0168 | 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 | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1269+562C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 10/21 | chr11 | 989251 | ||||||
| chr11:989281
|
C | T | 35 | a0001c0002t0002g0136a0001c0002t0002g0209a0001c0002t0002g0217others(32): Show | 35 | HG00544.hp2 HG00597.hp1 HG01069.hp2 others(32): 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 | a0001c0001t0003g0040 | 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 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0042others(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 | a0001c0002t0002g0004a0001c0005t0003g0177 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0116others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0064 | 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 | a0001c0002t0002g0234a0001c0002t0003g0186 | 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 | a0001c0003t0004g0256 | 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 | a0001c0001t0001g0044a0001c0002t0002g0004a0001c0003t0002g0196others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0003g0139 | 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 | a0001c0002t0003g0139 | 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 | a0001c0002t0003g0139 | 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 | a0001c0003t0002g0206 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0128others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0116a0001c0001t0001g0120 | 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 | a0001c0004t0009g0260a0001c0004t0009g0261 | 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 | a0001c0002t0003g0139 | 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 | a0001c0003t0002g0157 | 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 | a0001c0001t0001g0128 | 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 | a0001c0003t0002g0194 | 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 | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): 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 | a0001c0002t0001g0071a0001c0002t0002g0151a0001c0002t0002g0159others(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 | a0001c0002t0001g0071a0001c0002t0002g0151a0001c0002t0002g0159others(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 | a0001c0002t0005g0141a0001c0002t0005g0142a0001c0002t0005g0190others(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 | a0001c0002t0003g0172 | 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 | a0001c0002t0003g0172 | 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 | a0001c0002t0003g0182 | 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 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0258 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0078 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0162 | 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 | a0001c0001t0001g0122a0001c0001t0003g0129 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0011g0164 | 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 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0044others(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 | a0001c0002t0003g0201 | 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 | a0001c0001t0005g0083 | 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 | a0001c0001t0001g0112 | 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 | a0001c0003t0002g0145 | 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 | a0001c0003t0002g0145 | 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 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0229a0001c0002t0004g0253 | 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 | a0001c0001t0001g0122a0001c0001t0003g0129 | 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 | a0001c0001t0001g0114 | 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 | a0001c0003t0004g0256 | 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 | a0003c0007t0004g0225 | 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 | a0001c0002t0002g0226 | 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 | a0001c0003t0002g0222 | 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 | a0001c0001t0001g0092 | 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 | a0001c0002t0003g0139a0001c0002t0003g0172a0001c0003t0002g0206 | 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 | a0001c0002t0005g0141a0001c0002t0005g0142a0001c0002t0005g0190others(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 | a0001c0002t0004g0255 | 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 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0068others(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 | a0001c0003t0006g0135 | 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 | a0001c0001t0001g0114 | 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 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0207others(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 | a0001c0002t0003g0148 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0002t0002g0233others(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 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0017others(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 | a0001c0001t0001g0032a0001c0001t0001g0047a0001c0001t0001g0052others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0122 | 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 | 40 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0041others(37): Show | 40 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(37): 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 | a0001c0001t0005g0087a0001c0002t0002g0155 | 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 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0122others(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 | a0001c0002t0004g0224 | 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 | a0001c0008t0004g0237 | 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 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0002t0004g0224 | 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 | a0001c0003t0006g0264 | 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 | a0001c0003t0006g0264 | 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 | a0001c0003t0006g0264 | 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 | a0001c0003t0006g0264 | 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 | a0001c0002t0004g0224a0001c0003t0006g0264a0001c0005t0003g0140 | 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 | a0001c0003t0002g0145 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0112others(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 | a0001c0001t0013g0063 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0112others(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 | a0001c0001t0003g0102a0001c0001t0005g0081 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0075a0001c0001t0001g0114a0001c0001t0001g0123 | 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 | a0001c0005t0003g0140 | 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 | a0001c0001t0001g0092 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0113others(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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0001g0116a0001c0001t0005g0083a0001c0002t0003g0002others(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 | a0001c0001t0019g0020 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0003g0129others(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 | a0001c0001t0007g0089 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0002c0009t0003g0150 | 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 | a0002c0009t0003g0150 | 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 | a0001c0005t0003g0188 | 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 | a0001c0002t0002g0003a0001c0002t0002g0004 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0001g0121a0001c0001t0003g0102a0001c0002t0002g0245 | 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 | a0001c0002t0002g0003a0001c0002t0003g0172a0001c0003t0002g0206others(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 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0058others(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 | a0001c0001t0001g0029a0001c0001t0001g0085a0001c0001t0001g0104others(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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0003t0006g0264 | 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 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0075 | 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 | a0004c0014t0001g0262 | 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 | a0001c0001t0007g0089 | 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 | a0001c0001t0003g0102 | 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 | a0001c0002t0003g0202 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0049 | 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 | a0001c0004t0009g0261 | 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 | a0001c0001t0001g0034 | 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 | a0001c0002t0002g0248 | 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 | a0002c0009t0003g0150 | 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 | a0001c0002t0002g0168 | 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 | a0001c0001t0001g0122 | 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 | a0001c0002t0003g0148 | 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 | a0001c0002t0002g0161 | 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 | a0001c0006t0018g0099 | 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 | a0001c0002t0003g0147 | 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 | a0001c0002t0005g0190 | 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 | a0001c0001t0005g0083 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0004a0001c0004t0010g0165 | 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 | a0001c0004t0002g0192 | 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 | a0001c0003t0002g0212 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0027 | 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 | a0005c0011t0002g0243 | 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 | a0001c0001t0001g0112 | 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 | a0001c0002t0003g0184 | 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 | a0001c0001t0001g0047 | 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 |
6 | a0001c0001t0002g0053a0001c0002t0002g0136a0001c0002t0002g0217others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG03834.hp2 others(3): 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 | a0001c0002t0002g0209a0001c0003t0002g0134a0001c0003t0002g0193others(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 | a0001c0003t0002g0208 | 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 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0107a0001c0002t0003g0002 | 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 | a0001c0005t0003g0140 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0005g0084 | 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 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0005g0019others(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 | a0001c0001t0001g0115 | 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 | a0001c0002t0002g0245 | 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 | a0001c0002t0003g0201 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0002g0098 | 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 | a0001c0003t0002g0157 | 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 | a0001c0003t0002g0133a0001c0003t0002g0158 | 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 | a0001c0001t0001g0014 | 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 | a0001c0002t0002g0241 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0005g0152 | 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 | a0001c0003t0002g0194 | 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 | a0001c0002t0004g0230 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0128others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0003c0007t0004g0225 | 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 | a0001c0001t0001g0130 | 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 | a0001c0002t0004g0224 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0227others(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 | a0001c0002t0004g0229 | 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 | a0001c0002t0004g0255 | 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 | a0001c0002t0002g0234 | 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 | a0001c0002t0002g0257 | 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 | a0001c0002t0002g0235 | 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 | a0001c0001t0001g0041 | 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 | a0001c0003t0002g0205 | 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 | a0001c0002t0002g0252 | 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 | a0001c0003t0002g0206 | 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 | a0001c0001t0005g0081 | 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 | a0001c0002t0003g0001 | 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 | a0001c0001t0001g0121 | 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 | a0001c0003t0002g0145 | 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 | a0001c0001t0001g0021 | 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 | a0001c0008t0004g0237 | 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 | a0001c0001t0001g0078 | 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 | a0001c0004t0009g0260 | 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 | a0001c0002t0011g0164 | 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 | a0001c0003t0006g0264 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0044 | 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 | a0001c0002t0003g0172 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0120others(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 | a0001c0003t0002g0194 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0005g0081 | 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 | a0001c0001t0001g0047a0001c0004t0009g0261a0004c0014t0001g0262 | 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 | a0001c0002t0004g0224 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0014 | 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 | a0001c0003t0004g0256 | 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 | a0001c0002t0004g0223a0001c0002t0004g0228 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0061a0001c0001t0003g0102a0001c0002t0003g0172 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0122others(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 | a0001c0001t0005g0103a0001c0003t0006g0135a0001c0003t0006g0264others(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 | a0001c0002t0002g0143 | 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 | a0001c0001t0001g0050 | 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 | a0001c0002t0004g0227a0001c0002t0004g0229a0001c0002t0004g0236others(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 | 21 | a0001c0001t0002g0053a0001c0002t0002g0136a0001c0002t0002g0209others(18): Show | 21 | HG00544.hp2 HG00597.hp1 HG01069.hp2 others(18): 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0022 | 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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1957-2774G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 997658 | ||||||
| chr11:997733
|
C | T | 77 | a0001c0001t0002g0053a0001c0001t0003g0040a0001c0002t0002g0136others(74): Show | 77 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(74): 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0002t0002g0250 | 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 | a0001c0001t0013g0063 | 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 | a0001c0001t0001g0114a0001c0001t0005g0081a0001c0002t0003g0180 | 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 | a0001c0003t0002g0200 | 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 | a0001c0003t0004g0256 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(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 | a0001c0003t0002g0259 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0023a0001c0001t0001g0110 | 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 | a0001c0001t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1957-1879G>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998553 | ||||||
| chr11:998798
|
G | A | 267 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(264): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1957-1634G>A | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 14/21 | chr11 | 998798 | ||||||
| chr11:998835
|
A | G | 1 | a0001c0002t0002g0240 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0049others(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 | a0001c0002t0003g0172 | 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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0004t0010g0165 | 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 | a0001c0003t0004g0256 | 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 | a0001c0004t0009g0261 | 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 | a0001c0001t0007g0089a0001c0001t0007g0090a0001c0001t0007g0091 | 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 | a0001c0001t0001g0115 | 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 | a0001c0002t0004g0223 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0003t0002g0206 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0058others(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 | a0001c0001t0003g0102a0001c0001t0005g0019a0001c0001t0005g0081others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0003g0102a0001c0001t0005g0019a0001c0001t0005g0081others(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 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0047others(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 | a0001c0001t0001g0037a0001c0001t0001g0062 | 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 | a0001c0003t0002g0211 | 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 | a0001c0001t0001g0034a0001c0001t0001g0097 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0263 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0007g0090 | 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 | a0001c0002t0004g0227a0001c0002t0004g0255 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0002t0002g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2123+356C>T | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1000954 | ||||||
| chr11:1001275
|
T | C | 1 | a0001c0002t0002g0217 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2123+677T>C | AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 15/21 | chr11 | 1001275 | ||||||
| chr11:1001383
|
C | T | 1 | a0001c0006t0018g0099 | 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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0001t0003g0040a0001c0002t0003g0001a0001c0002t0003g0002others(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 | a0001c0002t0004g0229a0001c0002t0004g0253 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0003g0172 | 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 | a0001c0003t0002g0205 | 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 | a0001c0001t0003g0040a0001c0002t0003g0001a0001c0002t0003g0002others(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 | a0001c0001t0001g0010a0001c0001t0001g0086 | 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 | a0001c0001t0001g0047 | 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 | a0001c0003t0002g0205 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0001g0033a0001c0001t0001g0093 | 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 | a0001c0001t0015g0066 | 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 | a0001c0001t0001g0014 | 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 | a0001c0002t0003g0172 | 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 | a0001c0002t0003g0172 | 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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0003t0002g0238 | 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 | a0001c0003t0002g0145 | 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 | a0001c0001t0005g0081a0001c0002t0002g0242a0001c0002t0002g0248others(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 | a0001c0002t0003g0172 | 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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0003g0173 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0002g0053 | 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 | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0006g0008a0001c0001t0006g0009 | 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 | a0001c0002t0003g0184 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0226a0001c0002t0004g0223a0001c0002t0004g0224others(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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0002t0002g0162 | 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 | a0001c0003t0002g0205 | 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 | a0001c0002t0002g0136a0001c0002t0002g0221 | 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 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0046others(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 | a0001c0001t0001g0014 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0226a0001c0002t0002g0233a0001c0002t0002g0234others(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 | a0001c0001t0002g0053 | 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0001g0130 | 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 | a0001c0002t0004g0166 | 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 | a0001c0001t0001g0085a0001c0001t0001g0104 | 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 | a0001c0001t0001g0100 | 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 | a0001c0002t0004g0229a0001c0002t0004g0253a0001c0002t0004g0254 | 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 | a0001c0002t0002g0155 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0003t0006g0135a0001c0003t0006g0264a0001c0003t0006g0265others(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 | a0001c0004t0010g0165 | 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 | a0001c0001t0001g0012 | 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 | a0001c0004t0010g0165 | 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 | a0001c0006t0001g0126 | 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 | a0001c0004t0002g0191a0001c0004t0002g0192 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0001t0001g0067a0001c0001t0001g0124 | 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 | a0001c0003t0002g0205 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0029 | 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 | a0001c0006t0001g0036 | 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 | a0001c0001t0005g0019a0001c0001t0005g0081a0001c0001t0005g0082others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0001t0001g0047 | 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 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(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 | a0001c0005t0003g0131 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0046a0001c0003t0002g0193a0001c0003t0002g0205others(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 | a0001c0003t0002g0193a0001c0003t0002g0205a0001c0003t0002g0210others(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 | a0001c0003t0002g0193a0001c0003t0002g0205a0001c0003t0002g0210others(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 | a0001c0003t0002g0205 | 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 | a0001c0003t0002g0193a0001c0003t0002g0210a0001c0003t0002g0216others(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 | a0001c0002t0002g0226 | 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 | a0001c0001t0005g0019 | 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 | a0001c0002t0003g0184 | 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 |
20 | a0001c0001t0002g0053a0001c0002t0002g0136a0001c0002t0002g0204others(17): Show | 20 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(17): 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 | a0001c0003t0002g0203a0001c0003t0002g0222 | 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 | a0001c0002t0003g0186 | 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 | a0001c0003t0002g0193a0001c0003t0002g0205a0001c0003t0002g0210others(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 | a0001c0003t0002g0205 | 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 | a0001c0003t0002g0208 | 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 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0051others(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 | a0001c0003t0002g0194a0001c0003t0002g0199a0001c0003t0002g0200others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0005g0190 | 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 | a0001c0003t0002g0194a0001c0003t0002g0199a0001c0003t0002g0200others(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 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0245others(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 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0123others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0004g0223a0001c0002t0004g0224a0001c0002t0004g0227others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(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 | a0001c0002t0002g0242a0001c0002t0002g0247a0001c0002t0002g0251others(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 | a0001c0003t0002g0208 | 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 | a0001c0006t0001g0036 | 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 | a0001c0003t0002g0199a0001c0003t0002g0207a0001c0003t0002g0212others(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 |