Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11215 |
|---|---|
| ensemblid | ENSG00000023516.9 |
| hgncid | 369 |
| symbol | AKAP11 |
| name | A-kinase anchoring protein 11 |
| refseq_nuc | NM_016248.4 |
| refseq_prot | NP_057332.1 |
| ensembl_nuc | ENST00000025301.4 |
| ensembl_prot | ENSP00000025301.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 42272152 |
| end | 42323261 |
| strand | + |
| ver | v1.2 |
| region | chr13:42272152-42323261 |
| region5000 | chr13:42267152-42328261 |
| regionname0 | AKAP11_chr13_42272152_42323261 |
| regionname5000 | AKAP11_chr13_42267152_42328261 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1901 | 319 | 75 | 66 | 129 | 16 | 31 | 103 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002 | 0/0 | 1901 | 17 | 1 | 0 | 15 | 0 | 1 | 12 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003 | 0/0 | 1901 | 11 | 0 | 0 | 10 | 0 | 1 | 6 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0004 | 0/0 | 1901 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0005 | 0/0 | 1901 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0006 | 0/0 | 1901 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0007 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0008 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0009 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0010 | 0/0 | 1901 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0011 | 0/0 | 1901 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0012 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0013 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0014 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0015 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0016 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0017 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0018 | 0/0 | 1901 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0019 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0020 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0021 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0022 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0023 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5706 | 245 | 56 | 54 | 100 | 9 | 24 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0002 | 0/0 | 5706 | 38 | 1 | 5 | 26 | 3 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0003 | 0/0 | 5706 | 27 | 17 | 4 | 0 | 4 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0004 | 0/0 | 5706 | 17 | 1 | 0 | 15 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0005 | 0/0 | 5706 | 10 | 0 | 0 | 9 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0006 | 0/0 | 5706 | 4 | 0 | 2 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0007 | 0/0 | 5706 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0008 | 0/0 | 5706 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0009 | 0/0 | 5706 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0010 | 0/0 | 5706 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0011 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0012 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0013 | 0/0 | 5706 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0014 | 0/0 | 5706 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0015 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0016 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0017 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0018 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0019 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0020 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0021 | 0/0 | 5706 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0022 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0023 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0024 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0025 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0026 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0027 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0028 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0029 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| c0030 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4206 | 35 | 0 | 6 | 22 | 3 | 4 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0002 | 0/0 | 4212 | 22 | 8 | 0 | 10 | 0 | 4 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0003 | 0/0 | 4218 | 14 | 0 | 7 | 5 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0004 | 0/0 | 4216 | 13 | 1 | 1 | 11 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0005 | 0/0 | 4224 | 13 | 0 | 4 | 8 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0006 | 0/0 | 4216 | 13 | 0 | 6 | 5 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0007 | 1/0 | 4210 | 12 | 0 | 0 | 11 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0008 | 0/0 | 4208 | 12 | 0 | 0 | 12 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0009 | 0/0 | 4214 | 11 | 0 | 2 | 6 | 0 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0010 | 0/0 | 4212 | 10 | 2 | 4 | 0 | 3 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0011 | 0/0 | 4206 | 9 | 2 | 1 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0012 | 0/1 | 4208 | 9 | 0 | 5 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0013 | 0/0 | 4212 | 9 | 7 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0014 | 0/0 | 4220 | 9 | 0 | 4 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0015 | 0/0 | 4212 | 9 | 8 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0016 | 0/0 | 4222 | 9 | 0 | 6 | 0 | 3 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0017 | 0/0 | 4208 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0018 | 0/0 | 4208 | 8 | 2 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0019 | 0/0 | 4220 | 8 | 5 | 0 | 2 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0020 | 0/0 | 4222 | 8 | 2 | 2 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0021 | 0/0 | 4216 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0022 | 0/0 | 4210 | 7 | 5 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0023 | 0/0 | 4214 | 6 | 1 | 0 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0024 | 0/0 | 4226 | 6 | 0 | 1 | 3 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0025 | 0/0 | 4206 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0026 | 0/0 | 4218 | 5 | 0 | 3 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0027 | 0/0 | 4220 | 5 | 0 | 3 | 1 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0028 | 0/0 | 4214 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0029 | 0/0 | 4212 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0030 | 0/0 | 4214 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0031 | 0/0 | 4208 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0032 | 0/0 | 4218 | 3 | 1 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0033 | 0/0 | 4228 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0034 | 0/0 | 4216 | 3 | 2 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0035 | 0/0 | 4224 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0036 | 0/0 | 4186 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0037 | 0/0 | 4218 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0038 | 0/0 | 4208 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0039 | 0/0 | 4214 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0040 | 0/0 | 4210 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0041 | 0/0 | 4202 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0042 | 0/0 | 4208 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0043 | 0/0 | 4212 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0044 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0045 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0046 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0047 | 0/0 | 4216 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0048 | 0/0 | 4218 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0049 | 0/0 | 4220 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0050 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0051 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0052 | 0/0 | 4208 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0053 | 0/0 | 4208 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0054 | 0/0 | 4204 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0055 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0056 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0057 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0058 | 0/0 | 4218 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0059 | 0/0 | 4218 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0060 | 0/0 | 4210 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0061 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0062 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0063 | 0/0 | 4228 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0064 | 0/0 | 4220 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0065 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0066 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0067 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0068 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0069 | 0/0 | 4234 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0070 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0071 | 0/0 | 4224 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0072 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0073 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0074 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0075 | 0/0 | 4204 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0076 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0077 | 0/0 | 4210 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0078 | 0/0 | 4210 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0079 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0080 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0081 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0082 | 0/0 | 4216 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0083 | 0/0 | 4220 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0084 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0085 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0086 | 0/0 | 4224 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0087 | 0/0 | 4226 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0088 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0089 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0090 | 0/0 | 4210 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0091 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0092 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0093 | 0/0 | 4218 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0094 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0095 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| t0096 | 0/0 | 4218 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 24 | 0 | 6 | 15 | 1 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0002 | 0/0 | 21 | 0 | 5 | 11 | 0 | 5 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0003 | 0/0 | 13 | 0 | 0 | 9 | 0 | 4 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0004 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0006 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0007 | 0/1 | 8 | 0 | 5 | 0 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0010 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0012 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0017 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0023 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0048 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5706 | 245 | 56 | 54 | 100 | 9 | 24 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0002 | 0/0 | 5706 | 38 | 1 | 5 | 26 | 3 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003 | 0/0 | 5706 | 27 | 17 | 4 | 0 | 4 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0006 | 0/0 | 5706 | 4 | 0 | 2 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0010 | 0/0 | 5706 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0019 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0026 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002c0004 | 0/0 | 5706 | 17 | 1 | 0 | 15 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003c0005 | 0/0 | 5706 | 10 | 0 | 0 | 9 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003c0022 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0004c0009 | 0/0 | 5706 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0005c0007 | 0/0 | 5706 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0006c0008 | 0/0 | 5706 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0007c0015 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0008c0012 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0009c0011 | 0/0 | 5706 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0010c0013 | 0/0 | 5706 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0011c0014 | 0/0 | 5706 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0012c0028 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0013c0027 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0014c0023 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0015c0018 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0016c0029 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0017c0020 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0018c0021 | 0/0 | 5706 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0019c0017 | 0/0 | 5706 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0020c0024 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0021c0016 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0022c0025 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0023c0030 | 0/0 | 5706 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 9917 | 22 | 8 | 0 | 10 | 0 | 4 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0003 | 0/0 | 9923 | 14 | 0 | 7 | 5 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0004 | 0/0 | 9921 | 13 | 1 | 1 | 11 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0005 | 0/0 | 9929 | 13 | 0 | 4 | 8 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0006 | 0/0 | 9921 | 13 | 0 | 6 | 5 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0007 | 1/0 | 9915 | 9 | 0 | 0 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0009 | 0/0 | 9919 | 11 | 0 | 2 | 6 | 0 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0011 | 0/0 | 9911 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0012 | 0/1 | 9913 | 8 | 0 | 4 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0013 | 0/0 | 9917 | 8 | 7 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0014 | 0/0 | 9925 | 9 | 0 | 4 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0015 | 0/0 | 9917 | 9 | 8 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0016 | 0/0 | 9927 | 8 | 0 | 5 | 0 | 3 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0018 | 0/0 | 9913 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0019 | 0/0 | 9925 | 8 | 5 | 0 | 2 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0020 | 0/0 | 9927 | 8 | 2 | 2 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0021 | 0/0 | 9921 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0023 | 0/0 | 9919 | 6 | 1 | 0 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0024 | 0/0 | 9931 | 6 | 0 | 1 | 3 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0026 | 0/0 | 9923 | 3 | 0 | 3 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0027 | 0/0 | 9925 | 4 | 0 | 3 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0028 | 0/0 | 9919 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0029 | 0/0 | 9917 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0030 | 0/0 | 9919 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0031 | 0/0 | 9913 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0032 | 0/0 | 9923 | 3 | 1 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0033 | 0/0 | 9933 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0035 | 0/0 | 9929 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0036 | 0/0 | 9891 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0037 | 0/0 | 9923 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0043 | 0/0 | 9917 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0044 | 0/0 | 9917 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0045 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0046 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0047 | 0/0 | 9921 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0048 | 0/0 | 9923 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0050 | 0/0 | 9927 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0051 | 0/0 | 9901 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0052 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0053 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0054 | 0/0 | 9909 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0055 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0056 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0057 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0058 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0059 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0060 | 0/0 | 9915 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0061 | 0/0 | 9917 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0062 | 0/0 | 9927 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0063 | 0/0 | 9933 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0064 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0066 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0067 | 0/0 | 9937 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0068 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0069 | 0/0 | 9939 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0070 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0071 | 0/0 | 9929 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0074 | 0/0 | 9899 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0079 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0082 | 0/0 | 9921 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0083 | 0/0 | 9925 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0085 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0086 | 0/0 | 9929 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0087 | 0/0 | 9931 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0091 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0001t0093 | 0/0 | 9923 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0002t0001 | 0/0 | 9911 | 27 | 0 | 4 | 18 | 3 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0002t0017 | 0/0 | 9913 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0002t0088 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0002t0089 | 0/0 | 9913 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0010 | 0/0 | 9917 | 10 | 2 | 4 | 0 | 3 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0022 | 0/0 | 9915 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0025 | 0/0 | 9911 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0038 | 0/0 | 9913 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0077 | 0/0 | 9915 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0090 | 0/0 | 9915 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0094 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0003t0095 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0006t0001 | 0/0 | 9911 | 4 | 0 | 2 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0010t0016 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0010t0026 | 0/0 | 9923 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0019t0081 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0001c0026t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002c0004t0007 | 0/0 | 9915 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002c0004t0011 | 0/0 | 9911 | 6 | 0 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002c0004t0018 | 0/0 | 9913 | 7 | 1 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0002c0004t0042 | 0/0 | 9913 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003c0005t0008 | 0/0 | 9913 | 9 | 0 | 0 | 9 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003c0005t0075 | 0/0 | 9909 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0003c0022t0008 | 0/0 | 9913 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0004c0009t0072 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0004c0009t0073 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0004c0009t0080 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0005c0007t0034 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0005c0007t0039 | 0/0 | 9919 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0006c0008t0040 | 0/0 | 9915 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0006c0008t0092 | 0/0 | 9917 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0007c0015t0013 | 0/0 | 9917 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0007c0015t0028 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0008c0012t0034 | 0/0 | 9921 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0009c0011t0011 | 0/0 | 9911 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0010c0013t0008 | 0/0 | 9913 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0011c0014t0022 | 0/0 | 9915 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0012c0028t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0013c0027t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0014c0023t0078 | 0/0 | 9915 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0015c0018t0076 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0016c0029t0027 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0017c0020t0096 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0018c0021t0012 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0019c0017t0041 | 0/0 | 9907 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0020c0024t0049 | 0/0 | 9925 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0021c0016t0065 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0022c0025t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| a0023c0030t0084 | 0/0 | 9927 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | copy fasta | chr13 | 42267152 | 42328261 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0004g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0007g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0007g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0012g0007 | 0/1 | 7 | 0 | 4 | 0 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0015g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0020g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0021g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0021g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0023g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0023g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0023g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0024g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0024g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0026g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0027g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0027g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0027g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0028g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0028g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0029g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0029g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0029g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0030g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0031g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0032g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0032g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0033g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0033g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0035g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0035g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0035g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0036g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0036g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0037g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0037g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0043g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0044g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0045g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0046g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0047g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0048g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0050g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0051g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0052g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0053g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0054g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0055g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0056g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0057g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0058g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0059g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0060g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0061g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0062g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0063g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0064g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0066g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0067g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0068g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0069g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0070g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0071g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0074g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0079g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0082g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0083g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0085g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0086g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0087g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0091g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0001t0093g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0001 | 0/0 | 15 | 0 | 3 | 11 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0017g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0017g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0017g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0017g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0088g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0002t0089g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0023 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0022g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0022g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0025g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0025g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0025g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0038g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0077g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0090g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0094g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0003t0095g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0006t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0010t0016g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0010t0026g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0019t0081g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0001c0026t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0011g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0011g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0018g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0002c0004t0042g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0003c0005t0008g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0003c0005t0075g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0003c0022t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0004c0009t0072g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0004c0009t0073g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0004c0009t0080g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0005c0007t0034g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0005c0007t0039g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0005c0007t0039g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0006c0008t0040g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0006c0008t0092g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0007c0015t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0007c0015t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0008c0012t0034g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0009c0011t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0009c0011t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0010c0013t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0011c0014t0022g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0011c0014t0022g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0012c0028t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0013c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0014c0023t0078g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0015c0018t0076g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0016c0029t0027g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0017c0020t0096g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0018c0021t0012g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0019c0017t0041g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0020c0024t0049g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0021c0016t0065g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0022c0025t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| a0023c0030t0084g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0038 | g0017 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00099 | hp2 | a0001 | c0001 | t0016 | g0161 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0007 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0101 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00323 | hp1 | a0001 | c0003 | t0010 | g0023 | EUR | FIN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0157 | EUR | FIN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00408 | hp1 | a0002 | c0004 | t0007 | g0131 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00423 | hp1 | a0002 | c0004 | t0011 | g0011 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00423 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00438 | hp2 | a0001 | c0001 | t0029 | g0005 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00544 | hp1 | a0001 | c0001 | t0020 | g0175 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0075 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00597 | hp2 | a0001 | c0001 | t0033 | g0093 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00609 | hp1 | a0001 | c0001 | t0029 | g0078 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00609 | hp2 | a0010 | c0013 | t0008 | g0006 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00639 | hp2 | a0001 | c0003 | t0010 | g0017 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00642 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0007 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00735 | hp2 | a0001 | c0001 | t0035 | g0012 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00738 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0071 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01070 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01071 | hp1 | a0001 | c0002 | t0017 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01071 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0085 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01081 | hp1 | a0001 | c0001 | t0016 | g0162 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0159 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0103 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0025 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01109 | hp1 | a0009 | c0011 | t0011 | g0120 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01167 | hp1 | a0001 | c0001 | t0085 | g0012 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0080 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0007 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01243 | hp2 | a0001 | c0001 | t0052 | g0049 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01256 | hp1 | a0007 | c0015 | t0013 | g0180 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01256 | hp2 | a0001 | c0003 | t0010 | g0042 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01257 | hp1 | a0001 | c0001 | t0032 | g0004 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01257 | hp2 | a0001 | c0001 | t0026 | g0012 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01258 | hp1 | a0001 | c0001 | t0026 | g0012 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01258 | hp2 | a0001 | c0003 | t0010 | g0042 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01261 | hp1 | a0001 | c0001 | t0061 | g0070 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01261 | hp2 | a0018 | c0021 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01346 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01346 | hp2 | a0001 | c0001 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01361 | hp1 | a0001 | c0003 | t0010 | g0145 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01361 | hp2 | a0001 | c0001 | t0020 | g0092 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01496 | hp1 | a0001 | c0001 | t0016 | g0165 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01496 | hp2 | a0001 | c0001 | t0053 | g0049 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01515 | hp2 | a0001 | c0001 | t0027 | g0158 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01516 | hp1 | a0001 | c0001 | t0083 | g0167 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01516 | hp2 | a0001 | c0003 | t0010 | g0023 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0052 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01517 | hp2 | a0001 | c0003 | t0010 | g0142 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01884 | hp1 | a0001 | c0003 | t0022 | g0148 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01884 | hp2 | a0001 | c0001 | t0020 | g0072 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01891 | hp1 | a0001 | c0001 | t0086 | g0137 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01891 | hp2 | a0004 | c0009 | t0072 | g0172 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01928 | hp2 | a0001 | c0001 | t0093 | g0010 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01943 | hp1 | a0001 | c0001 | t0033 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01943 | hp2 | a0001 | c0001 | t0027 | g0025 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01952 | hp1 | a0001 | c0001 | t0087 | g0044 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01975 | hp1 | a0001 | c0001 | t0027 | g0107 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01975 | hp2 | a0001 | c0001 | t0015 | g0109 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01978 | hp2 | a0001 | c0001 | t0016 | g0044 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01981 | hp1 | a0001 | c0001 | t0009 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01981 | hp2 | a0008 | c0012 | t0034 | g0035 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01993 | hp2 | a0001 | c0001 | t0027 | g0025 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02004 | hp1 | a0001 | c0001 | t0047 | g0125 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02015 | hp1 | a0002 | c0004 | t0011 | g0135 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02015 | hp2 | a0001 | c0001 | t0044 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02074 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02083 | hp2 | a0001 | c0001 | t0091 | g0166 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02132 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02135 | hp1 | a0001 | c0001 | t0014 | g0095 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0177 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02145 | hp2 | a0004 | c0009 | t0080 | g0173 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02148 | hp1 | a0001 | c0001 | t0060 | g0097 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02148 | hp2 | a0001 | c0010 | t0016 | g0045 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02155 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02165 | hp1 | a0003 | c0022 | t0008 | g0198 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02165 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02257 | hp2 | a0001 | c0003 | t0010 | g0043 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0184 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02258 | hp2 | a0001 | c0003 | t0010 | g0043 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02293 | hp1 | a0011 | c0014 | t0022 | g0150 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02293 | hp2 | a0001 | c0001 | t0024 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02300 | hp2 | a0001 | c0001 | t0026 | g0012 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02451 | hp1 | a0001 | c0003 | t0022 | g0147 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02451 | hp2 | a0002 | c0004 | t0018 | g0133 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02523 | hp1 | a0001 | c0001 | t0068 | g0002 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02523 | hp2 | a0001 | c0001 | t0035 | g0164 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02572 | hp1 | a0001 | c0003 | t0025 | g0144 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02602 | hp1 | a0001 | c0003 | t0038 | g0017 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02615 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0183 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02622 | hp1 | a0001 | c0003 | t0090 | g0017 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0185 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0112 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0186 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02647 | hp2 | a0008 | c0012 | t0034 | g0035 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02698 | hp1 | a0001 | c0006 | t0001 | g0053 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02698 | hp2 | a0001 | c0001 | t0071 | g0062 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02717 | hp2 | a0001 | c0003 | t0022 | g0149 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02735 | hp1 | a0014 | c0023 | t0078 | g0199 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02735 | hp2 | a0001 | c0001 | t0012 | g0118 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0029 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02809 | hp2 | a0001 | c0001 | t0055 | g0189 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02818 | hp1 | a0001 | c0003 | t0025 | g0024 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02886 | hp2 | a0001 | c0003 | t0025 | g0024 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02895 | hp1 | a0001 | c0003 | t0022 | g0143 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02895 | hp2 | a0001 | c0001 | t0057 | g0190 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02896 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02897 | hp1 | a0001 | c0003 | t0022 | g0146 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02922 | hp1 | a0004 | c0009 | t0073 | g0174 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02922 | hp2 | a0023 | c0030 | t0084 | g0193 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02965 | hp1 | a0009 | c0011 | t0011 | g0117 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02965 | hp2 | a0001 | c0003 | t0025 | g0024 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0197 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02976 | hp2 | a0001 | c0001 | t0036 | g0124 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0068 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03017 | hp2 | a0001 | c0001 | t0013 | g0048 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0169 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0033 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03098 | hp2 | a0005 | c0007 | t0034 | g0141 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03139 | hp1 | a0001 | c0003 | t0094 | g0156 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0181 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03195 | hp1 | a0001 | c0001 | t0036 | g0039 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03195 | hp2 | a0001 | c0001 | t0074 | g0138 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03225 | hp2 | a0001 | c0001 | t0028 | g0187 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03239 | hp1 | a0001 | c0001 | t0024 | g0002 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03239 | hp2 | a0001 | c0001 | t0024 | g0102 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03453 | hp1 | a0001 | c0001 | t0028 | g0104 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0033 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03486 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03491 | hp1 | a0001 | c0001 | t0056 | g0031 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03491 | hp2 | a0001 | c0001 | t0048 | g0003 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03516 | hp1 | a0017 | c0020 | t0096 | g0153 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0064 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03540 | hp1 | a0001 | c0001 | t0015 | g0111 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03540 | hp2 | a0001 | c0019 | t0081 | g0171 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03579 | hp1 | a0001 | c0001 | t0058 | g0188 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03579 | hp2 | a0005 | c0007 | t0039 | g0140 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03654 | hp1 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03654 | hp2 | a0001 | c0001 | t0063 | g0094 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03710 | hp1 | a0001 | c0002 | t0088 | g0001 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03831 | hp1 | a0015 | c0018 | t0076 | g0106 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03834 | hp1 | a0001 | c0003 | t0010 | g0023 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0001 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03942 | hp2 | a0001 | c0001 | t0050 | g0003 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04184 | hp1 | a0001 | c0001 | t0082 | g0012 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0002 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0128 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04199 | hp2 | a0002 | c0004 | t0042 | g0132 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04204 | hp1 | a0003 | c0005 | t0075 | g0063 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04204 | hp2 | a0019 | c0017 | t0041 | g0196 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04228 | hp1 | a0001 | c0001 | t0043 | g0114 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18522 | hp1 | a0001 | c0002 | t0089 | g0051 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18522 | hp2 | a0001 | c0001 | t0067 | g0021 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0003 | EAS | CHB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18612 | hp2 | a0001 | c0001 | t0051 | g0002 | EAS | CHB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18906 | hp1 | a0001 | c0001 | t0046 | g0015 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0067 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18939 | hp1 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18939 | hp2 | a0002 | c0004 | t0018 | g0136 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18940 | hp1 | a0013 | c0027 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18940 | hp2 | a0001 | c0001 | t0064 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18941 | hp1 | a0012 | c0028 | t0001 | g0059 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18944 | hp1 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18944 | hp2 | a0022 | c0025 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18945 | hp2 | a0006 | c0008 | t0040 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18946 | hp2 | a0001 | c0001 | t0029 | g0030 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18947 | hp2 | a0001 | c0001 | t0023 | g0129 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18948 | hp1 | a0006 | c0008 | t0092 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18950 | hp1 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18950 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18951 | hp1 | a0021 | c0016 | t0065 | g0034 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18957 | hp2 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18961 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18961 | hp2 | a0001 | c0001 | t0014 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18962 | hp2 | a0001 | c0026 | t0001 | g0027 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18966 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18967 | hp1 | a0001 | c0001 | t0037 | g0096 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18969 | hp2 | a0001 | c0010 | t0026 | g0046 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18972 | hp1 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18972 | hp2 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18978 | hp2 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18979 | hp1 | a0002 | c0004 | t0011 | g0041 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18979 | hp2 | a0001 | c0001 | t0021 | g0099 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18980 | hp1 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18982 | hp2 | a0001 | c0001 | t0054 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18983 | hp1 | a0001 | c0001 | t0019 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18983 | hp2 | a0001 | c0001 | t0019 | g0091 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18985 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18986 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18992 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18992 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18993 | hp1 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0065 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18994 | hp1 | a0002 | c0004 | t0011 | g0040 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18999 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19000 | hp1 | a0001 | c0001 | t0035 | g0163 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19000 | hp2 | a0001 | c0001 | t0033 | g0098 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19001 | hp1 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19001 | hp2 | a0001 | c0001 | t0021 | g0088 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19003 | hp2 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19005 | hp1 | a0001 | c0001 | t0037 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19007 | hp1 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19010 | hp2 | a0001 | c0001 | t0029 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19012 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19030 | hp1 | a0001 | c0001 | t0069 | g0021 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19030 | hp2 | a0020 | c0024 | t0049 | g0126 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19043 | hp1 | a0001 | c0001 | t0059 | g0048 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0179 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19054 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19055 | hp1 | a0001 | c0001 | t0070 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19056 | hp1 | a0006 | c0008 | t0040 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19056 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19058 | hp1 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19058 | hp2 | a0001 | c0001 | t0021 | g0030 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19062 | hp1 | a0001 | c0010 | t0026 | g0046 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19062 | hp2 | a0001 | c0001 | t0021 | g0089 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19064 | hp1 | a0002 | c0004 | t0011 | g0040 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19065 | hp1 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19065 | hp2 | a0001 | c0001 | t0020 | g0084 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19067 | hp1 | a0001 | c0002 | t0017 | g0050 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19067 | hp2 | a0001 | c0001 | t0066 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19070 | hp2 | a0016 | c0029 | t0027 | g0045 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19077 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19079 | hp1 | a0002 | c0004 | t0007 | g0134 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19081 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19082 | hp1 | a0002 | c0004 | t0007 | g0122 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19084 | hp1 | a0001 | c0002 | t0017 | g0054 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19084 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19085 | hp1 | a0010 | c0013 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19086 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19086 | hp2 | a0001 | c0002 | t0017 | g0060 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19091 | hp1 | a0002 | c0004 | t0011 | g0041 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA19240 | hp2 | a0005 | c0007 | t0039 | g0139 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20129 | hp1 | a0001 | c0001 | t0062 | g0100 | AFR | ASW | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20129 | hp2 | a0001 | c0003 | t0025 | g0155 | AFR | ASW | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0069 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20752 | hp2 | a0001 | c0001 | t0016 | g0160 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20805 | hp1 | a0001 | c0001 | t0012 | g0007 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01123 | hp1 | a0011 | c0014 | t0022 | g0151 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0077 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02109 | hp1 | a0001 | c0003 | t0025 | g0154 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02109 | hp2 | a0001 | c0001 | t0031 | g0016 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0116 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0182 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03471 | hp1 | a0007 | c0015 | t0028 | g0178 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG03471 | hp2 | a0001 | c0001 | t0079 | g0108 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG06807 | hp1 | a0001 | c0003 | t0095 | g0152 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0176 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18955 | hp1 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA18955 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA20300 | hp2 | a0001 | c0001 | t0032 | g0031 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA21309 | hp1 | a0001 | c0001 | t0045 | g0015 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| NA21309 | hp2 | a0001 | c0003 | t0077 | g0113 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0007 | REF | REF | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0168 | REF | REF | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42297145
|
A | G | 1 | a0023 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.314A>G | p.Asn105Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/13 | 490/9915 | 314/5706 | 105/1901 | chr13 | 42297145 | ||
| chr13:42298660
|
T | C | 1 | a0022 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.479T>C | p.Leu160Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 655/9915 | 479/5706 | 160/1901 | chr13 | 42298660 | ||
| chr13:42300231
|
T | G | 1 | a0021 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1485T>G | p.Ile495Met | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1661/9915 | 1485/5706 | 495/1901 | chr13 | 42300231 | ||
| chr13:42300554
|
G | A | 1 | a0023 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1808G>A | p.Arg603His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1984/9915 | 1808/5706 | 603/1901 | chr13 | 42300554 | ||
| chr13:42300574
|
C | T | 1 | a0004 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.1828C>T | p.Arg610Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2004/9915 | 1828/5706 | 610/1901 | chr13 | 42300574 | ||
| chr13:42300908
|
C | G | 1 | a0012 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.2162C>G | p.Ser721Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2338/9915 | 2162/5706 | 721/1901 | chr13 | 42300908 | ||
| chr13:42300911
|
C | T | 1 | a0013 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2165C>T | p.Thr722Met | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2341/9915 | 2165/5706 | 722/1901 | chr13 | 42300911 | ||
| chr13:42300953
|
C | T | 1 | a0007 | 2 | HG01256.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.2207C>T | p.Ser736Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2383/9915 | 2207/5706 | 736/1901 | chr13 | 42300953 | ||
| chr13:42300989
|
A | G | 1 | a0020 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2243A>G | p.Asn748Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2419/9915 | 2243/5706 | 748/1901 | chr13 | 42300989 | ||
| chr13:42301410
|
A | T | 1 | a0014 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.2664A>T | p.Leu888Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2840/9915 | 2664/5706 | 888/1901 | chr13 | 42301410 | ||
| chr13:42301451
|
A | G | 1 | a0011 | 2 | HG01123.hp1 HG02293.hp1 |
missense_variant | MODERATE | c.2705A>G | p.Glu902Gly | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2881/9915 | 2705/5706 | 902/1901 | chr13 | 42301451 | ||
| chr13:42301454
|
G | A | 1 | a0015 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2708G>A | p.Arg903His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2884/9915 | 2708/5706 | 903/1901 | chr13 | 42301454 | ||
| chr13:42301547
|
A | G | 1 | a0019 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.2801A>G | p.Asn934Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2977/9915 | 2801/5706 | 934/1901 | chr13 | 42301547 | ||
| chr13:42301585
|
A | G | 2 | a0003a0010 | 13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
missense_variant | MODERATE | c.2839A>G | p.Ile947Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3015/9915 | 2839/5706 | 947/1901 | chr13 | 42301585 | ||
| chr13:42301834
|
A | G | 1 | a0008 | 2 | HG01981.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.3088A>G | p.Thr1030Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3264/9915 | 3088/5706 | 1030/1901 | chr13 | 42301834 | ||
| chr13:42301967
|
C | T | 1 | a0002 | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
missense_variant | MODERATE | c.3221C>T | p.Ser1074Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3397/9915 | 3221/5706 | 1074/1901 | chr13 | 42301967 | ||
| chr13:42301991
|
G | T | 1 | a0006 | 3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
missense_variant | MODERATE | c.3245G>T | p.Gly1082Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3421/9915 | 3245/5706 | 1082/1901 | chr13 | 42301991 | ||
| chr13:42302074
|
C | T | 1 | a0018 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.3328C>T | p.Arg1110Trp | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3504/9915 | 3328/5706 | 1110/1901 | chr13 | 42302074 | ||
| chr13:42302479
|
T | A | 1 | a0015 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.3733T>A | p.Phe1245Ile | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3909/9915 | 3733/5706 | 1245/1901 | chr13 | 42302479 | ||
| chr13:42302725
|
T | C | 1 | a0010 | 2 | HG00609.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.3979T>C | p.Cys1327Arg | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4155/9915 | 3979/5706 | 1327/1901 | chr13 | 42302725 | ||
| chr13:42302860
|
G | A | 1 | a0017 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.4114G>A | p.Ala1372Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4290/9915 | 4114/5706 | 1372/1901 | chr13 | 42302860 | ||
| chr13:42302976
|
A | C | 1 | a0005 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.4230A>C | p.Leu1410Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4406/9915 | 4230/5706 | 1410/1901 | chr13 | 42302976 | ||
| chr13:42303004
|
G | A | 1 | a0015 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.4258G>A | p.Glu1420Lys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4434/9915 | 4258/5706 | 1420/1901 | chr13 | 42303004 | ||
| chr13:42303121
|
A | G | 1 | a0023 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.4375A>G | p.Thr1459Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4551/9915 | 4375/5706 | 1459/1901 | chr13 | 42303121 | ||
| chr13:42303572
|
A | C | 1 | a0015 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.4826A>C | p.Gln1609Pro | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5002/9915 | 4826/5706 | 1609/1901 | chr13 | 42303572 | ||
| chr13:42303615
|
T | G | 1 | a0014 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.4869T>G | p.Phe1623Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5045/9915 | 4869/5706 | 1623/1901 | chr13 | 42303615 | ||
| chr13:42303622
|
C | T | 1 | a0009 | 2 | HG01109.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.4876C>T | p.Arg1626Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5052/9915 | 4876/5706 | 1626/1901 | chr13 | 42303622 | ||
| chr13:42303713
|
C | T | 1 | a0016 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.4967C>T | p.Ala1656Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5143/9915 | 4967/5706 | 1656/1901 | chr13 | 42303713 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42298580
|
A | G | 2 | a0001c0010a0016c0029 | 4 | HG02148.hp2 NA18969.hp2 NA19062.hp1 others(1): Show |
synonymous_variant | LOW | c.399A>G | p.Ser133Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 575/9915 | 399/5706 | 133/1901 | chr13 | 42298580 | ||
| chr13:42298583
|
A | G | 6 | a0001c0002a0001c0006a0001c0026others(3): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.402A>G | p.Pro134Pro | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 578/9915 | 402/5706 | 134/1901 | chr13 | 42298583 | ||
| chr13:42298643
|
C | T | 6 | a0001c0002a0001c0006a0001c0026others(3): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 638/9915 | 462/5706 | 154/1901 | chr13 | 42298643 | ||
| chr13:42299646
|
G | A | 1 | a0001c0006 | 4 | HG00642.hp1 HG00738.hp1 HG02698.hp1 others(1): Show |
synonymous_variant | LOW | c.900G>A | p.Ser300Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1076/9915 | 900/5706 | 300/1901 | chr13 | 42299646 | ||
| chr13:42301122
|
T | C | 1 | a0019c0017 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.2376T>C | p.Tyr792Tyr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2552/9915 | 2376/5706 | 792/1901 | chr13 | 42301122 | ||
| chr13:42302154
|
A | C | 3 | a0001c0003a0011c0014a0017c0020 | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
synonymous_variant | LOW | c.3408A>C | p.Thr1136Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3584/9915 | 3408/5706 | 1136/1901 | chr13 | 42302154 | ||
| chr13:42303129
|
G | C | 11 | a0001c0002a0001c0006a0001c0026others(8): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
synonymous_variant | LOW | c.4383G>C | p.Leu1461Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4559/9915 | 4383/5706 | 1461/1901 | chr13 | 42303129 | ||
| chr13:42303252
|
C | T | 1 | a0001c0026 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.4506C>T | p.His1502His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4682/9915 | 4506/5706 | 1502/1901 | chr13 | 42303252 | ||
| chr13:42303501
|
A | G | 1 | a0003c0022 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.4755A>G | p.Gln1585Gln | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4931/9915 | 4755/5706 | 1585/1901 | chr13 | 42303501 | ||
| chr13:42303690
|
A | G | 1 | a0001c0019 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.4944A>G | p.Ala1648Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5120/9915 | 4944/5706 | 1648/1901 | chr13 | 42303690 | ||
| chr13:42308484
|
C | T | 6 | a0001c0002a0001c0006a0001c0026others(3): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.5148C>T | p.Thr1716Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/13 | 5324/9915 | 5148/5706 | 1716/1901 | chr13 | 42308484 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42272175
|
C | T | 3 | a0001c0003t0094a0001c0003t0095a0017c0020t0096 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-153C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/13 | chr13 | 42272175 | ||||||
| chr13:42286333
|
A | G | 1 | a0001c0001t0093 | 1 | HG01928.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-16A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/13 | chr13 | 42286333 | ||||||
| chr13:42319338
|
G | T | 2 | a0006c0008t0040a0006c0008t0092 | 3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*110G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 110 | chr13 | 42319338 | |||||
| chr13:42319619
|
T | C | 1 | a0019c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*391T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 391 | chr13 | 42319619 | |||||
| chr13:42319669
|
A | T | 1 | a0001c0001t0091 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*441A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 441 | chr13 | 42319669 | |||||
| chr13:42319708
|
C | CCTTT | 91 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(88): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*482_*485dupTTTC | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 486 | INFO_REALIGN_3_PRIME | chr13 | 42319708 | ||||
| chr13:42319717
|
T | C | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(38): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*489T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 489 | chr13 | 42319717 | |||||
| chr13:42319741
|
A | T | 1 | a0001c0001t0071 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*513A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 513 | chr13 | 42319741 | |||||
| chr13:42319747
|
C | T | 1 | a0001c0003t0090 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 519 | chr13 | 42319747 | |||||
| chr13:42319850
|
C | T | 9 | a0001c0002t0001a0001c0002t0017a0001c0002t0088others(6): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 622 | chr13 | 42319850 | |||||
| chr13:42319906
|
G | GGT | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(11): Show | 55 | HG00140.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*722dupGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGT | 8 | a0001c0001t0023a0001c0001t0026a0001c0001t0032others(5): Show | 18 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*722dupGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGT | 7 | a0001c0001t0019a0001c0001t0027a0001c0001t0029others(4): Show | 20 | HG00438.hp2 HG00609.hp1 HG01261.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*717_*722dupGTGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(1): Show |
10 | a0001c0001t0009a0001c0001t0016a0001c0001t0020others(7): Show | 37 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*715_*722dupGTGTGT others(2): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(3): Show |
7 | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(4): Show | 39 | HG00140.hp2 HG00408.hp2 HG00735.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*722dupGTGTGT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(5): Show |
6 | a0001c0001t0003a0001c0001t0024a0001c0001t0037others(3): Show | 25 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*711_*722dupGTGTGT others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(7): Show |
4 | a0001c0001t0014a0001c0001t0033a0001c0001t0063others(1): Show | 14 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*709_*722dupGTGTGT others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(9): Show |
2 | a0001c0001t0066a0021c0016t0065 | 2 | NA18951.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*707_*722dupGTGTGT others(10): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(11): Show |
2 | a0001c0001t0067a0001c0001t0068 | 2 | HG02523.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*705_*722dupGTGTGT others(12): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
G | GGTGTGTG others(13): Show |
2 | a0001c0001t0069a0001c0001t0070 | 2 | NA19030.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*703_*722dupGTGTGT others(14): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGT | G | 9 | a0001c0001t0013a0001c0001t0015a0001c0001t0018others(6): Show | 39 | HG00323.hp1 HG00639.hp2 HG01256.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*722delGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 721 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGT | G | 9 | a0001c0001t0011a0001c0003t0022a0001c0003t0025others(6): Show | 25 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*722delGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 719 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGT | G | 9 | a0001c0001t0031a0001c0001t0052a0001c0001t0053others(6): Show | 30 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*717_*722delGTGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 717 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGTG others(1): Show |
G | 9 | a0001c0002t0001a0001c0002t0088a0001c0006t0001others(6): Show | 38 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*715_*722delGTGTGT others(2): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 715 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGTG others(3): Show |
G | 1 | a0003c0005t0075 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713_*722delGTGTGT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 713 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0051 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705_*722delGTGTGT others(12): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 705 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703_*722delGTGTGT others(14): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 703 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319906
|
GGTGTGTG others(17): Show |
G | 1 | a0001c0001t0036 | 2 | HG02976.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699_*722delGTGTGT others(18): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 699 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | ||||
| chr13:42319909
|
G | A | 1 | a0004c0009t0073 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 681 | chr13 | 42319909 | |||||
| chr13:42319911
|
G | A | 1 | a0004c0009t0072 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 683 | chr13 | 42319911 | |||||
| chr13:42319973
|
AGTTT | A | 2 | a0001c0001t0012a0018c0021t0012 | 9 | HG00140.hp1 HG00733.hp2 HG01243.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*749_*752delTGTT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 749 | INFO_REALIGN_3_PRIME | chr13 | 42319973 | ||||
| chr13:42320002
|
T | C | 1 | a0001c0001t0058 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 774 | chr13 | 42320002 | |||||
| chr13:42320061
|
A | C | 1 | a0015c0018t0076 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 833 | chr13 | 42320061 | |||||
| chr13:42320099
|
A | T | 1 | a0002c0004t0042 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 871 | chr13 | 42320099 | |||||
| chr13:42320100
|
T | A | 1 | a0001c0003t0077 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 872 | chr13 | 42320100 | |||||
| chr13:42320131
|
T | C | 1 | a0001c0001t0062 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 903 | chr13 | 42320131 | |||||
| chr13:42320151
|
A | T | 9 | a0001c0002t0001a0001c0002t0017a0001c0002t0088others(6): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*923A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 923 | chr13 | 42320151 | |||||
| chr13:42320232
|
A | G | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(38): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*1004A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1004 | chr13 | 42320232 | |||||
| chr13:42320249
|
T | C | 1 | a0001c0001t0043 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1021 | chr13 | 42320249 | |||||
| chr13:42320259
|
G | A | 76 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(73): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1031 | chr13 | 42320259 | |||||
| chr13:42320262
|
G | T | 1 | a0019c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1034 | chr13 | 42320262 | |||||
| chr13:42320269
|
T | G | 1 | a0005c0007t0039 | 2 | HG03579.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1041 | chr13 | 42320269 | |||||
| chr13:42320269
|
TTTTGTTT others(1): Show |
T | 18 | a0001c0001t0003a0001c0001t0006a0001c0001t0009others(15): Show | 74 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1057_*1064delGTTT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1057 | INFO_REALIGN_3_PRIME | chr13 | 42320269 | ||||
| chr13:42320273
|
G | T | 11 | a0001c0001t0016a0001c0001t0026a0001c0001t0027others(8): Show | 26 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1045G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1045 | chr13 | 42320273 | |||||
| chr13:42320277
|
G | T | 1 | a0001c0001t0085 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1049 | chr13 | 42320277 | |||||
| chr13:42320278
|
T | G | 1 | a0001c0001t0085 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1050T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1050 | chr13 | 42320278 | |||||
| chr13:42320321
|
G | A | 1 | a0001c0001t0059 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1093G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1093 | chr13 | 42320321 | |||||
| chr13:42320341
|
A | G | 3 | a0001c0003t0094a0001c0003t0095a0017c0020t0096 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1113A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1113 | chr13 | 42320341 | |||||
| chr13:42320386
|
C | G | 1 | a0001c0001t0046 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1158 | chr13 | 42320386 | |||||
| chr13:42320452
|
C | A | 3 | a0004c0009t0072a0004c0009t0073a0004c0009t0080 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1224C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1224 | chr13 | 42320452 | |||||
| chr13:42320491
|
T | C | 1 | a0001c0001t0044 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1263T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1263 | chr13 | 42320491 | |||||
| chr13:42320508
|
C | T | 1 | a0001c0003t0077 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1280C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1280 | chr13 | 42320508 | |||||
| chr13:42320671
|
T | G | 2 | a0001c0002t0088a0015c0018t0076 | 2 | HG03710.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1443T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1443 | chr13 | 42320671 | |||||
| chr13:42320817
|
G | A | 1 | a0019c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1589 | chr13 | 42320817 | |||||
| chr13:42321030
|
C | T | 76 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(73): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1802 | chr13 | 42321030 | |||||
| chr13:42321119
|
T | G | 1 | a0023c0030t0084 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1891T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1891 | chr13 | 42321119 | |||||
| chr13:42321407
|
C | T | 1 | a0001c0001t0045 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2179C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2179 | chr13 | 42321407 | |||||
| chr13:42321434
|
T | C | 1 | a0001c0002t0089 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2206 | chr13 | 42321434 | |||||
| chr13:42321456
|
CACTT | C | 1 | a0001c0003t0025 | 6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2231_*2234delTTAC | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2231 | INFO_REALIGN_3_PRIME | chr13 | 42321456 | ||||
| chr13:42321458
|
C | G | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2230C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2230 | chr13 | 42321458 | |||||
| chr13:42321462
|
C | T | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2234C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2234 | chr13 | 42321462 | |||||
| chr13:42321592
|
T | G | 15 | a0001c0002t0001a0001c0002t0017a0001c0002t0088others(12): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2364T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2364 | chr13 | 42321592 | |||||
| chr13:42321703
|
A | G | 1 | a0001c0002t0089 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2475A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2475 | chr13 | 42321703 | |||||
| chr13:42321856
|
G | A | 10 | a0001c0003t0010a0001c0003t0022a0001c0003t0025others(7): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2628G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2628 | chr13 | 42321856 | |||||
| chr13:42321963
|
T | C | 15 | a0001c0002t0001a0001c0002t0017a0001c0002t0088others(12): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2735T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2735 | chr13 | 42321963 | |||||
| chr13:42322007
|
T | C | 1 | a0001c0001t0052 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2779T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2779 | chr13 | 42322007 | |||||
| chr13:42322054
|
A | G | 3 | a0001c0001t0055a0001c0001t0057a0001c0001t0058 | 3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2826A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2826 | chr13 | 42322054 | |||||
| chr13:42322081
|
A | G | 1 | a0023c0030t0084 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2853 | chr13 | 42322081 | |||||
| chr13:42322252
|
T | G | 5 | a0003c0005t0008a0003c0005t0075a0003c0022t0008others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3024 | chr13 | 42322252 | |||||
| chr13:42322287
|
A | G | 6 | a0001c0001t0021a0001c0001t0029a0001c0001t0030others(3): Show | 19 | HG00438.hp2 HG00609.hp1 HG02165.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3059A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3059 | chr13 | 42322287 | |||||
| chr13:42322423
|
A | G | 1 | a0001c0001t0031 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3195A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3195 | chr13 | 42322423 | |||||
| chr13:42322609
|
A | T | 1 | a0001c0001t0086 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3381 | chr13 | 42322609 | |||||
| chr13:42322669
|
T | G | 1 | a0003c0005t0075 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3441T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3441 | chr13 | 42322669 | |||||
| chr13:42322770
|
T | C | 1 | a0001c0001t0063 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3542T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3542 | chr13 | 42322770 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42272302
|
G | A | 23 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(20): Show | 45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-100+74G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272302 | ||||||
| chr13:42272347
|
C | G | 4 | a0003c0005t0008g0006a0003c0022t0008g0198a0010c0013t0008g0006others(1): Show | 13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-100+119C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272347 | ||||||
| chr13:42272418
|
G | A | 1 | a0001c0001t0071g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-100+190G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272418 | ||||||
| chr13:42272527
|
C | T | 1 | a0001c0001t0018g0197 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100+299C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272527 | ||||||
| chr13:42272570
|
G | C | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-100+342G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272570 | ||||||
| chr13:42272587
|
GCGTGGTG others(19): Show |
G | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+367_-100+392d others(28): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42272587 | |||||
| chr13:42272668
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-100+440C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272668 | ||||||
| chr13:42272878
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+650G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272878 | ||||||
| chr13:42272905
|
C | T | 1 | a0001c0001t0005g0194 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-100+677C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272905 | ||||||
| chr13:42273278
|
T | A | 1 | a0003c0022t0008g0198 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-100+1050T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273278 | ||||||
| chr13:42273298
|
T | G | 90 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(87): Show | 117 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-100+1070T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273298 | ||||||
| chr13:42273357
|
AT | A | 8 | a0001c0001t0009g0065a0001c0001t0019g0064a0001c0001t0027g0107others(5): Show | 17 | HG00423.hp2 HG00609.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.-100+1143delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42273357 | |||||
| chr13:42273592
|
C | G | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-100+1364C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273592 | ||||||
| chr13:42273689
|
G | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+1461G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273689 | ||||||
| chr13:42273724
|
A | T | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100+1496A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273724 | ||||||
| chr13:42273800
|
T | A | 1 | a0001c0003t0077g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-100+1572T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273800 | ||||||
| chr13:42273913
|
T | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(42): Show | 77 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-100+1685T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273913 | ||||||
| chr13:42274140
|
G | T | 1 | a0001c0001t0004g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-100+1912G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274140 | ||||||
| chr13:42274292
|
G | T | 1 | a0002c0004t0018g0136 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-100+2064G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274292 | ||||||
| chr13:42274329
|
C | T | 1 | a0001c0001t0015g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-100+2101C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274329 | ||||||
| chr13:42274446
|
G | A | 4 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(1): Show | 13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-100+2218G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274446 | ||||||
| chr13:42274470
|
G | C | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-100+2242G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274470 | ||||||
| chr13:42274510
|
C | T | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-100+2282C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274510 | ||||||
| chr13:42274511
|
C | T | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+2283C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274511 | ||||||
| chr13:42274663
|
C | A | 146 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(143): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-100+2435C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274663 | ||||||
| chr13:42274663
|
C | CGACTGAG others(63): Show |
1 | a0001c0001t0016g0157 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-100+2488_-100+248 others(74): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42274663 | |||||
| chr13:42274708
|
T | C | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-100+2480T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274708 | ||||||
| chr13:42274717
|
G | A | 23 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(20): Show | 27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100+2489G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274717 | ||||||
| chr13:42274849
|
T | G | 1 | a0001c0001t0043g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-100+2621T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274849 | ||||||
| chr13:42274928
|
C | A | 1 | a0014c0023t0078g0199 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-100+2700C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274928 | ||||||
| chr13:42275005
|
G | T | 3 | a0004c0009t0072g0172a0004c0009t0073g0174a0004c0009t0080g0173 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-100+2777G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275005 | ||||||
| chr13:42275079
|
C | T | 1 | a0001c0003t0094g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-100+2851C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275079 | ||||||
| chr13:42275189
|
A | G | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-100+2961A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275189 | ||||||
| chr13:42275292
|
A | G | 1 | a0001c0001t0004g0191 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-100+3064A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275292 | ||||||
| chr13:42275369
|
A | G | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-100+3141A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275369 | ||||||
| chr13:42275414
|
T | A | 2 | a0001c0001t0003g0019a0001c0001t0014g0019 | 3 | NA18939.hp1 NA18947.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-100+3186T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275414 | ||||||
| chr13:42275426
|
A | G | 3 | a0001c0003t0025g0024a0001c0003t0025g0154a0001c0003t0025g0155 | 5 | HG02109.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100+3198A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275426 | ||||||
| chr13:42275679
|
C | T | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+3451C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275679 | ||||||
| chr13:42275750
|
C | A | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+3522C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275750 | ||||||
| chr13:42275808
|
G | A | 121 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(118): Show | 158 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.-100+3580G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275808 | ||||||
| chr13:42275906
|
T | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0115 | 3 | HG02155.hp1 NA18973.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-100+3678T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275906 | ||||||
| chr13:42276046
|
T | G | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-100+3818T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276046 | ||||||
| chr13:42276404
|
G | T | 3 | a0001c0001t0055g0189a0001c0001t0057g0190a0001c0001t0058g0188 | 3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-100+4176G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276404 | ||||||
| chr13:42276484
|
C | A | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-100+4256C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276484 | ||||||
| chr13:42276507
|
A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100+4279A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276507 | ||||||
| chr13:42276564
|
T | G | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+4336T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276564 | ||||||
| chr13:42276675
|
A | G | 1 | a0001c0019t0081g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-100+4447A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276675 | ||||||
| chr13:42276713
|
T | C | 23 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(20): Show | 27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100+4485T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276713 | ||||||
| chr13:42276894
|
T | C | 1 | a0001c0001t0013g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-100+4666T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276894 | ||||||
| chr13:42276923
|
G | C | 1 | a0001c0001t0023g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-100+4695G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276923 | ||||||
| chr13:42277013
|
G | T | 1 | a0001c0001t0014g0105 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-100+4785G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277013 | ||||||
| chr13:42277034
|
A | T | 2 | a0002c0004t0011g0041a0002c0004t0011g0135 | 3 | HG02015.hp1 NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-100+4806A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277034 | ||||||
| chr13:42277070
|
T | C | 2 | a0001c0001t0005g0029a0001c0001t0019g0029 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-100+4842T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277070 | ||||||
| chr13:42277070
|
T | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100+4842T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277070 | ||||||
| chr13:42277135
|
A | G | 35 | a0001c0001t0003g0010a0001c0001t0006g0010a0001c0001t0009g0010others(32): Show | 68 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-100+4907A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277135 | ||||||
| chr13:42277138
|
T | C | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100+4910T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277138 | ||||||
| chr13:42277198
|
A | C | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-100+4970A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277198 | ||||||
| chr13:42277364
|
A | G | 1 | a0001c0003t0010g0043 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-100+5136A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277364 | ||||||
| chr13:42277572
|
G | A | 11 | a0001c0001t0002g0015a0001c0001t0002g0037a0001c0001t0002g0119others(8): Show | 20 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-100+5344G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277572 | ||||||
| chr13:42277653
|
G | A | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+5425G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277653 | ||||||
| chr13:42277727
|
G | A | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-100+5499G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277727 | ||||||
| chr13:42277747
|
A | G | 2 | a0001c0001t0013g0067a0001c0001t0028g0104 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-100+5519A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277747 | ||||||
| chr13:42277903
|
T | C | 9 | a0001c0001t0004g0004a0001c0001t0004g0047a0001c0001t0004g0191others(6): Show | 19 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-100+5675T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277903 | ||||||
| chr13:42277972
|
A | G | 1 | a0001c0001t0028g0187 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-100+5744A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277972 | ||||||
| chr13:42278163
|
C | G | 3 | a0001c0003t0025g0024a0001c0003t0025g0154a0001c0003t0025g0155 | 5 | HG02109.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100+5935C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278163 | ||||||
| chr13:42278284
|
C | T | 3 | a0001c0003t0094g0156a0001c0003t0095g0152a0017c0020t0096g0153 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-100+6056C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278284 | ||||||
| chr13:42278376
|
A | C | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6148A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278376 | ||||||
| chr13:42278377
|
G | C | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6149G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278377 | ||||||
| chr13:42278378
|
G | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6150G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278378 | ||||||
| chr13:42278379
|
A | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6151A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278379 | ||||||
| chr13:42278380
|
A | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6152A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278380 | ||||||
| chr13:42278384
|
A | G | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6156A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278384 | ||||||
| chr13:42278755
|
G | A | 1 | a0001c0001t0009g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-100+6527G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278755 | ||||||
| chr13:42278853
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-100+6625C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278853 | ||||||
| chr13:42278931
|
C | T | 1 | a0001c0001t0028g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-100+6703C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278931 | ||||||
| chr13:42278931
|
CT | C | 3 | a0001c0001t0007g0008a0001c0001t0007g0121a0001c0001t0014g0105 | 9 | NA18946.hp1 NA18959.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.-100+6715delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42278931 | |||||
| chr13:42278941
|
T | C | 1 | a0001c0002t0017g0050 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-100+6713T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278941 | ||||||
| chr13:42278982
|
T | C | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+6754T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278982 | ||||||
| chr13:42278989
|
C | T | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+6761C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278989 | ||||||
| chr13:42279005
|
G | A | 1 | a0001c0001t0079g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-100+6777G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279005 | ||||||
| chr13:42279169
|
A | G | 1 | a0001c0001t0006g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-99-6817A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279169 | ||||||
| chr13:42279216
|
T | TA | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-99-6770_-99-6769i others(3): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279216 | ||||||
| chr13:42279263
|
C | CCA | 63 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(60): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-99-6705_-99-6704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | |||||
| chr13:42279263
|
C | CCACACA | 22 | a0001c0002t0001g0001a0001c0002t0001g0027a0001c0002t0001g0028others(19): Show | 43 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-99-6709_-99-6704d others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | |||||
| chr13:42279263
|
C | CCACACAC others(1): Show |
2 | a0001c0002t0001g0026a0001c0002t0001g0052 | 3 | HG01515.hp1 HG01517.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-99-6711_-99-6704d others(10): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | |||||
| chr13:42279263
|
CCA | C | 4 | a0001c0001t0005g0029a0001c0001t0019g0029a0001c0001t0062g0100others(1): Show | 4 | HG02602.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-6705_-99-6704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | |||||
| chr13:42279265
|
A | C | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-99-6721A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279265 | ||||||
| chr13:42279281
|
A | ACT | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-6693_-99-6692d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279281 | |||||
| chr13:42279281
|
A | T | 2 | a0001c0001t0006g0101a0015c0018t0076g0106 | 2 | HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-99-6705A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279281 | ||||||
| chr13:42279281
|
ACT | A | 3 | a0005c0007t0034g0141a0005c0007t0039g0139a0005c0007t0039g0140 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-99-6693_-99-6692d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279281 | |||||
| chr13:42279283
|
T | A | 35 | a0001c0002t0089g0051a0001c0003t0010g0017a0001c0003t0010g0023others(32): Show | 48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-99-6703T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279283 | ||||||
| chr13:42279285
|
T | A | 22 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(19): Show | 29 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-99-6701T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279285 | ||||||
| chr13:42279287
|
T | A | 3 | a0001c0003t0094g0156a0001c0003t0095g0152a0017c0020t0096g0153 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-99-6699T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279287 | ||||||
| chr13:42279291
|
TCTCA | T | 3 | a0001c0001t0055g0189a0001c0001t0057g0190a0001c0001t0058g0188 | 3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-99-6683_-99-6680d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279291 | |||||
| chr13:42279293
|
TCA | T | 10 | a0002c0004t0007g0131a0002c0004t0007g0134a0002c0004t0011g0011others(7): Show | 16 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-99-6691_-99-6690d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279293 | |||||
| chr13:42279295
|
A | T | 24 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(21): Show | 31 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-99-6691A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279295 | ||||||
| chr13:42279307
|
G | T | 1 | a0001c0003t0022g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-99-6679G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279307 | ||||||
| chr13:42279351
|
T | C | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99-6635T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279351 | ||||||
| chr13:42279371
|
C | T | 1 | a0001c0001t0019g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-99-6615C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279371 | ||||||
| chr13:42279504
|
G | A | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-6482G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279504 | ||||||
| chr13:42279535
|
G | A | 2 | a0001c0003t0010g0023a0001c0003t0010g0142 | 4 | HG00323.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-6451G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279535 | ||||||
| chr13:42279615
|
A | G | 24 | a0001c0001t0031g0016a0001c0003t0010g0017a0001c0003t0010g0023others(21): Show | 34 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-99-6371A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279615 | ||||||
| chr13:42279767
|
T | A | 1 | a0011c0014t0022g0150 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-99-6219T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279767 | ||||||
| chr13:42279855
|
G | A | 210 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(207): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.-99-6131G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279855 | ||||||
| chr13:42279911
|
C | T | 3 | a0005c0007t0034g0141a0005c0007t0039g0139a0005c0007t0039g0140 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-99-6075C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279911 | ||||||
| chr13:42279926
|
T | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-6060T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279926 | ||||||
| chr13:42280208
|
C | T | 1 | a0001c0001t0091g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-99-5778C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280208 | ||||||
| chr13:42280231
|
C | T | 1 | a0001c0002t0001g0028 | 2 | HG00597.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-99-5755C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280231 | ||||||
| chr13:42280392
|
A | G | 1 | a0001c0001t0021g0099 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-99-5594A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280392 | ||||||
| chr13:42280476
|
C | T | 1 | a0001c0001t0033g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-99-5510C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280476 | ||||||
| chr13:42280503
|
A | G | 210 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(207): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.-99-5483A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280503 | ||||||
| chr13:42280537
|
C | A | 3 | a0001c0001t0006g0069a0001c0001t0006g0071a0001c0001t0061g0070 | 3 | HG00741.hp1 HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-99-5449C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280537 | ||||||
| chr13:42280546
|
T | C | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-99-5440T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280546 | ||||||
| chr13:42280798
|
T | C | 4 | a0001c0001t0003g0013a0001c0001t0006g0013a0001c0001t0009g0013others(1): Show | 5 | HG00642.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99-5188T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280798 | ||||||
| chr13:42280957
|
T | C | 3 | a0001c0001t0002g0036a0001c0001t0002g0115a0001c0001t0002g0123 | 4 | HG02155.hp1 NA18973.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-5029T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280957 | ||||||
| chr13:42281293
|
G | C | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-99-4693G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281293 | ||||||
| chr13:42281468
|
C | A | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-99-4518C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281468 | ||||||
| chr13:42281980
|
C | CT | 43 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(40): Show | 75 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-99-3990dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42281980 | |||||
| chr13:42281983
|
T | TC | 9 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0066others(6): Show | 13 | HG00642.hp2 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99-4003_-99-4002i others(3): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281983 | ||||||
| chr13:42281984
|
T | C | 107 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0019others(104): Show | 140 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-99-4002T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281984 | ||||||
| chr13:42282008
|
G | A | 1 | a0001c0001t0006g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-99-3978G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282008 | ||||||
| chr13:42282102
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-99-3884G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282102 | ||||||
| chr13:42282104
|
G | A | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-99-3882G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282104 | ||||||
| chr13:42282260
|
C | CT | 11 | a0001c0001t0004g0047a0001c0001t0004g0192a0001c0001t0007g0008others(8): Show | 18 | HG01496.hp1 HG02056.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.-99-3704dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | |||||
| chr13:42282260
|
C | CTT | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99-3705_-99-3704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | |||||
| chr13:42282260
|
CT | C | 29 | a0001c0001t0015g0109a0001c0001t0021g0030a0001c0001t0027g0107others(26): Show | 51 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-99-3704delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | |||||
| chr13:42282308
|
A | T | 256 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(253): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-99-3678A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282308 | ||||||
| chr13:42282489
|
T | C | 145 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(142): Show | 192 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.-99-3497T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282489 | ||||||
| chr13:42282562
|
A | T | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-3424A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282562 | ||||||
| chr13:42282669
|
A | G | 6 | a0001c0001t0005g0029a0001c0001t0019g0029a0001c0001t0062g0100others(3): Show | 6 | HG02602.hp2 HG02698.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99-3317A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282669 | ||||||
| chr13:42283115
|
C | G | 1 | a0001c0001t0002g0037 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-99-2871C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283115 | ||||||
| chr13:42283144
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-2842C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283144 | ||||||
| chr13:42283146
|
C | T | 2 | a0001c0001t0052g0049a0001c0001t0053g0049 | 2 | HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-99-2840C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283146 | ||||||
| chr13:42283360
|
CA | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-2625delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283360 | ||||||
| chr13:42283385
|
A | G | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-2601A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283385 | ||||||
| chr13:42283436
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-2550G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283436 | ||||||
| chr13:42283651
|
A | G | 4 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(1): Show | 13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99-2335A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283651 | ||||||
| chr13:42283765
|
A | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-2221A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283765 | ||||||
| chr13:42283830
|
G | A | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-99-2156G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283830 | ||||||
| chr13:42284001
|
G | A | 11 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0007g0134others(8): Show | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99-1985G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284001 | ||||||
| chr13:42284028
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-1958A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284028 | ||||||
| chr13:42284130
|
G | A | 2 | a0011c0014t0022g0150a0011c0014t0022g0151 | 2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-99-1856G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284130 | ||||||
| chr13:42284254
|
T | C | 11 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0007g0134others(8): Show | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99-1732T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284254 | ||||||
| chr13:42284331
|
C | T | 1 | a0001c0001t0015g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-99-1655C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284331 | ||||||
| chr13:42284644
|
CA | C | 4 | a0001c0001t0013g0182a0001c0001t0013g0184a0009c0011t0011g0117others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-1339delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42284644 | |||||
| chr13:42284714
|
A | G | 1 | a0001c0001t0074g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-99-1272A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284714 | ||||||
| chr13:42285433
|
A | G | 1 | a0002c0004t0007g0134 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-99-553A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285433 | ||||||
| chr13:42285543
|
T | C | 1 | a0001c0001t0020g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-99-443T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285543 | ||||||
| chr13:42285788
|
T | TATATTTG others(9): Show |
1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-196_-99-195ins others(16): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285788 | |||||
| chr13:42285791
|
C | T | 1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-195C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285791 | ||||||
| chr13:42285793
|
A | G | 1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-193A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285793 | ||||||
| chr13:42285805
|
A | G | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-99-181A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285805 | ||||||
| chr13:42285819
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-99-167C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285819 | ||||||
| chr13:42285869
|
C | CATAGAGA others(4): Show |
1 | a0001c0001t0013g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-99-116_-99-115ins others(11): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285869 | |||||
| chr13:42285871
|
C | G | 1 | a0001c0001t0013g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-99-115C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285871 | ||||||
| chr13:42285882
|
G | A | 1 | a0001c0001t0058g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-99-104G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285882 | ||||||
| chr13:42285905
|
A | AG | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-99-78dupG | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285905 | |||||
| chr13:42286038
|
A | G | 1 | a0005c0007t0034g0141 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.-50+3A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 2/12 | chr13 | 42286038 | ||||||
| chr13:42286559
|
A | G | 1 | a0001c0001t0074g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+160A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286559 | ||||||
| chr13:42286601
|
G | A | 1 | a0001c0001t0062g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.51+202G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286601 | ||||||
| chr13:42286834
|
G | A | 1 | a0001c0001t0047g0125 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51+435G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286834 | ||||||
| chr13:42286901
|
C | A | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+502C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286901 | ||||||
| chr13:42286941
|
G | T | 3 | a0001c0001t0020g0021a0001c0001t0067g0021a0001c0001t0069g0021 | 3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51+542G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286941 | ||||||
| chr13:42287111
|
C | T | 1 | a0001c0019t0081g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.51+712C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287111 | ||||||
| chr13:42287209
|
A | G | 1 | a0001c0003t0022g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.51+810A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287209 | ||||||
| chr13:42287228
|
C | T | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.51+829C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287228 | ||||||
| chr13:42287290
|
T | A | 2 | a0001c0001t0005g0073a0001c0001t0005g0074 | 2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.51+891T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287290 | ||||||
| chr13:42287300
|
T | C | 3 | a0004c0009t0072g0172a0004c0009t0073g0174a0004c0009t0080g0173 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.51+901T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287300 | ||||||
| chr13:42287301
|
T | G | 2 | a0001c0001t0028g0187a0019c0017t0041g0196 | 2 | HG03225.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.51+902T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287301 | ||||||
| chr13:42287475
|
G | A | 120 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(117): Show | 157 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.51+1076G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287475 | ||||||
| chr13:42287486
|
G | A | 26 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(23): Show | 30 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.51+1087G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287486 | ||||||
| chr13:42287536
|
G | A | 45 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(42): Show | 77 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.51+1137G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287536 | ||||||
| chr13:42287575
|
C | T | 1 | a0001c0001t0015g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.51+1176C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287575 | ||||||
| chr13:42287576
|
G | T | 1 | a0001c0001t0033g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.51+1177G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287576 | ||||||
| chr13:42287626
|
A | AT | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1229dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr13 | 42287626 | |||||
| chr13:42287636
|
A | C | 27 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(24): Show | 31 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.51+1237A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287636 | ||||||
| chr13:42287714
|
T | C | 3 | a0001c0003t0094g0156a0001c0003t0095g0152a0017c0020t0096g0153 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.51+1315T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287714 | ||||||
| chr13:42287813
|
T | C | 1 | a0001c0001t0061g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.51+1414T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287813 | ||||||
| chr13:42287883
|
C | T | 1 | a0001c0001t0019g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1484C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287883 | ||||||
| chr13:42288113
|
A | G | 3 | a0001c0010t0016g0045a0001c0010t0026g0046a0016c0029t0027g0045 | 4 | HG02148.hp2 NA18969.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1714A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288113 | ||||||
| chr13:42288119
|
A | G | 1 | a0001c0001t0020g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.51+1720A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288119 | ||||||
| chr13:42288287
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1888C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288287 | ||||||
| chr13:42288422
|
T | G | 1 | a0001c0003t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.51+2023T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288422 | ||||||
| chr13:42288425
|
A | G | 1 | a0001c0001t0079g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51+2026A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288425 | ||||||
| chr13:42288637
|
CT | C | 7 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0011g0011others(4): Show | 13 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+2239delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288637 | ||||||
| chr13:42288736
|
A | C | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+2337A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288736 | ||||||
| chr13:42288780
|
T | A | 1 | a0002c0004t0042g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+2381T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288780 | ||||||
| chr13:42288813
|
T | G | 8 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 13 | HG01975.hp2 HG01981.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+2414T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288813 | ||||||
| chr13:42288902
|
G | T | 1 | a0001c0001t0019g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+2503G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288902 | ||||||
| chr13:42288909
|
A | C | 2 | a0001c0001t0074g0138a0001c0001t0086g0137 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2510A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288909 | ||||||
| chr13:42289103
|
T | C | 4 | a0001c0003t0025g0024a0001c0003t0025g0144a0001c0003t0025g0154others(1): Show | 6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+2704T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289103 | ||||||
| chr13:42289222
|
T | G | 1 | a0001c0001t0083g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.51+2823T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289222 | ||||||
| chr13:42289425
|
T | G | 1 | a0001c0001t0016g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.52-2960T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289425 | ||||||
| chr13:42289498
|
T | G | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-2887T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289498 | ||||||
| chr13:42289526
|
C | G | 1 | a0007c0015t0013g0180 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.52-2859C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289526 | ||||||
| chr13:42289558
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0043a0001c0003t0022g0143others(6): Show | 11 | HG00099.hp1 HG00639.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.52-2827C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289558 | ||||||
| chr13:42289616
|
T | C | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-2769T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289616 | ||||||
| chr13:42289770
|
C | T | 2 | a0001c0001t0016g0025a0001c0001t0027g0025 | 3 | HG01106.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.52-2615C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289770 | ||||||
| chr13:42289820
|
C | G | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.52-2565C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289820 | ||||||
| chr13:42290330
|
C | T | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52-2055C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290330 | ||||||
| chr13:42290457
|
T | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-1928T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290457 | ||||||
| chr13:42290526
|
C | T | 1 | a0001c0001t0019g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52-1859C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290526 | ||||||
| chr13:42290601
|
T | G | 1 | a0005c0007t0039g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52-1784T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290601 | ||||||
| chr13:42290717
|
A | G | 3 | a0001c0001t0020g0021a0001c0001t0067g0021a0001c0001t0069g0021 | 3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.52-1668A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290717 | ||||||
| chr13:42290774
|
A | G | 1 | a0001c0001t0019g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52-1611A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290774 | ||||||
| chr13:42290893
|
T | C | 2 | a0006c0008t0040g0022a0006c0008t0092g0022 | 3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.52-1492T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290893 | ||||||
| chr13:42290932
|
C | G | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.52-1453C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290932 | ||||||
| chr13:42291012
|
G | A | 1 | a0008c0012t0034g0035 | 2 | HG01981.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.52-1373G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291012 | ||||||
| chr13:42291050
|
C | T | 1 | a0004c0009t0080g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-1335C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291050 | ||||||
| chr13:42291061
|
C | G | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.52-1324C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291061 | ||||||
| chr13:42291378
|
G | A | 1 | a0005c0007t0034g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52-1007G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291378 | ||||||
| chr13:42291400
|
G | A | 11 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0007g0134others(8): Show | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-985G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291400 | ||||||
| chr13:42291415
|
G | A | 5 | a0001c0001t0003g0010a0001c0001t0006g0010a0001c0001t0009g0010others(2): Show | 7 | HG01928.hp2 HG03834.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.52-970G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291415 | ||||||
| chr13:42291454
|
T | G | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-931T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291454 | ||||||
| chr13:42291527
|
G | A | 45 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(42): Show | 77 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.52-858G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291527 | ||||||
| chr13:42291926
|
T | G | 1 | a0005c0007t0034g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52-459T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291926 | ||||||
| chr13:42292015
|
C | T | 1 | a0001c0001t0047g0125 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52-370C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292015 | ||||||
| chr13:42292045
|
C | T | 121 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(118): Show | 158 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.52-340C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292045 | ||||||
| chr13:42292047
|
G | A | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-338G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292047 | ||||||
| chr13:42292106
|
A | T | 3 | a0001c0001t0006g0020a0001c0001t0014g0020a0001c0001t0070g0020 | 3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-279A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292106 | ||||||
| chr13:42292134
|
A | T | 3 | a0001c0001t0006g0020a0001c0001t0014g0020a0001c0001t0070g0020 | 3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-251A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292134 | ||||||
| chr13:42292204
|
A | G | 3 | a0004c0009t0072g0172a0004c0009t0073g0174a0004c0009t0080g0173 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.52-181A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292204 | ||||||
| chr13:42292253
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.52-132G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292253 | ||||||
| chr13:42292282
|
A | G | 1 | a0012c0028t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.52-103A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292282 | ||||||
| chr13:42292324
|
C | G | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-61C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292324 | ||||||
| chr13:42292346
|
A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-39A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292346 | ||||||
| chr13:42292609
|
G | A | 1 | a0001c0001t0047g0125 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.168+108G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292609 | ||||||
| chr13:42292654
|
GA | G | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+161delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 42292654 | |||||
| chr13:42292659
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.168+158A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292659 | ||||||
| chr13:42292858
|
A | G | 1 | a0001c0001t0035g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168+357A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292858 | ||||||
| chr13:42292973
|
A | G | 1 | a0001c0001t0013g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.168+472A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292973 | ||||||
| chr13:42292981
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.168+480A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292981 | ||||||
| chr13:42293417
|
C | T | 1 | a0001c0003t0010g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+916C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293417 | ||||||
| chr13:42293714
|
G | A | 1 | a0001c0001t0020g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.168+1213G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293714 | ||||||
| chr13:42293750
|
C | T | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+1249C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293750 | ||||||
| chr13:42293818
|
A | G | 147 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(144): Show | 194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.168+1317A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293818 | ||||||
| chr13:42293830
|
T | G | 1 | a0001c0001t0035g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168+1329T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293830 | ||||||
| chr13:42293842
|
G | A | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+1341G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293842 | ||||||
| chr13:42293844
|
G | T | 1 | a0005c0007t0039g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+1343G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293844 | ||||||
| chr13:42293962
|
G | C | 256 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(253): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.168+1461G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293962 | ||||||
| chr13:42294005
|
A | G | 1 | a0001c0001t0091g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168+1504A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294005 | ||||||
| chr13:42294031
|
A | G | 1 | a0001c0003t0025g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+1530A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294031 | ||||||
| chr13:42294072
|
C | A | 23 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(20): Show | 27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+1571C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294072 | ||||||
| chr13:42294444
|
C | G | 2 | a0001c0001t0013g0067a0001c0001t0028g0104 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169-1251C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294444 | ||||||
| chr13:42294476
|
C | A | 1 | a0001c0001t0013g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-1219C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294476 | ||||||
| chr13:42294572
|
T | G | 23 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(20): Show | 27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-1123T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294572 | ||||||
| chr13:42294601
|
A | C | 2 | a0001c0003t0022g0147a0001c0003t0022g0149 | 2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.169-1094A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294601 | ||||||
| chr13:42294698
|
G | A | 2 | a0001c0001t0032g0031a0001c0001t0056g0031 | 2 | HG03491.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169-997G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294698 | ||||||
| chr13:42294748
|
A | C | 1 | a0001c0001t0002g0119 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169-947A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294748 | ||||||
| chr13:42294983
|
A | G | 23 | a0001c0001t0016g0025a0001c0001t0016g0044a0001c0001t0016g0157others(20): Show | 27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-712A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294983 | ||||||
| chr13:42295080
|
A | G | 1 | a0001c0001t0011g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169-615A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295080 | ||||||
| chr13:42295145
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169-550G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295145 | ||||||
| chr13:42295349
|
G | A | 3 | a0001c0001t0016g0159a0001c0001t0016g0160a0001c0001t0016g0161 | 3 | HG00099.hp2 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.169-346G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295349 | ||||||
| chr13:42295562
|
T | C | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-133T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295562 | ||||||
| chr13:42295584
|
A | AG | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.169-110dupG | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 42295584 | |||||
| chr13:42295874
|
C | T | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.216+132C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42295874 | ||||||
| chr13:42295880
|
G | A | 2 | a0001c0003t0022g0143a0001c0003t0022g0146 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+138G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42295880 | ||||||
| chr13:42296123
|
C | G | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.216+381C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296123 | ||||||
| chr13:42296185
|
A | G | 2 | a0001c0001t0091g0166a0001c0002t0001g0058 | 2 | HG01081.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.216+443A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296185 | ||||||
| chr13:42296205
|
A | G | 1 | a0001c0019t0081g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.216+463A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296205 | ||||||
| chr13:42296277
|
G | A | 256 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(253): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.216+535G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296277 | ||||||
| chr13:42296395
|
A | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.216+653A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296395 | ||||||
| chr13:42296548
|
C | T | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.217-500C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296548 | ||||||
| chr13:42296667
|
A | G | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.217-381A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296667 | ||||||
| chr13:42296713
|
AAAGTT | A | 51 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(48): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.217-326_217-322del others(5): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 42296713 | |||||
| chr13:42296837
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.217-211G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296837 | ||||||
| chr13:42297288
|
A | G | 1 | a0003c0005t0075g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.351+106A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297288 | ||||||
| chr13:42297326
|
A | G | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.351+144A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297326 | ||||||
| chr13:42297367
|
G | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+185G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297367 | ||||||
| chr13:42297543
|
C | T | 1 | a0001c0001t0023g0129 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.351+361C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297543 | ||||||
| chr13:42297624
|
TTTATAAA others(8): Show |
T | 1 | a0001c0001t0005g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.351+446_351+460del others(15): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 42297624 | |||||
| chr13:42297738
|
T | G | 1 | a0001c0003t0010g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.351+556T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297738 | ||||||
| chr13:42297768
|
C | A | 1 | a0001c0001t0029g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.351+586C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297768 | ||||||
| chr13:42297844
|
C | G | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.351+662C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297844 | ||||||
| chr13:42297888
|
A | ATTTAC | 211 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(208): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.352-642_352-641ins others(5): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 42297888 | |||||
| chr13:42297989
|
T | C | 1 | a0001c0001t0014g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.352-544T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297989 | ||||||
| chr13:42298127
|
G | A | 1 | a0002c0004t0007g0131 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.352-406G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298127 | ||||||
| chr13:42298189
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.352-344A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298189 | ||||||
| chr13:42298515
|
T | C | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-18T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298515 | ||||||
| chr13:42299028
|
C | T | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.616+231C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299028 | ||||||
| chr13:42299212
|
A | G | 1 | a0001c0001t0016g0161 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.617-151A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299212 | ||||||
| chr13:42299218
|
A | C | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.617-145A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299218 | ||||||
| chr13:42304242
|
A | T | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5117+379A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304242 | ||||||
| chr13:42304256
|
C | T | 76 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(73): Show | 102 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.5117+393C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304256 | ||||||
| chr13:42304305
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5117+442A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304305 | ||||||
| chr13:42304354
|
A | G | 6 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0011g0011others(3): Show | 11 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.5117+491A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304354 | ||||||
| chr13:42304423
|
G | A | 1 | a0001c0003t0095g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5117+560G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304423 | ||||||
| chr13:42304486
|
A | G | 2 | a0007c0015t0013g0180a0007c0015t0028g0178 | 2 | HG01256.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5117+623A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304486 | ||||||
| chr13:42304619
|
C | T | 1 | a0001c0001t0019g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+756C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304619 | ||||||
| chr13:42304620
|
T | G | 1 | a0001c0001t0019g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+757T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304620 | ||||||
| chr13:42304621
|
C | A | 1 | a0001c0001t0019g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+758C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304621 | ||||||
| chr13:42304622
|
T | A | 1 | a0001c0001t0019g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+759T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304622 | ||||||
| chr13:42304644
|
T | C | 3 | a0005c0007t0034g0141a0005c0007t0039g0139a0005c0007t0039g0140 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5117+781T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304644 | ||||||
| chr13:42304755
|
C | CT | 32 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(29): Show | 62 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.5117+905dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 42304755 | |||||
| chr13:42304907
|
C | T | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+1044C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304907 | ||||||
| chr13:42305030
|
C | T | 2 | a0001c0001t0005g0029a0001c0001t0019g0029 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.5117+1167C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305030 | ||||||
| chr13:42305094
|
G | C | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.5117+1231G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305094 | ||||||
| chr13:42305158
|
A | G | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5117+1295A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305158 | ||||||
| chr13:42305213
|
T | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(20): Show | 45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.5117+1350T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305213 | ||||||
| chr13:42305285
|
T | C | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5117+1422T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305285 | ||||||
| chr13:42305358
|
T | A | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+1495T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305358 | ||||||
| chr13:42305400
|
A | G | 33 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(30): Show | 59 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.5117+1537A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305400 | ||||||
| chr13:42305437
|
A | G | 1 | a0001c0010t0026g0046 | 2 | NA18969.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.5117+1574A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305437 | ||||||
| chr13:42305441
|
G | T | 29 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(26): Show | 60 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.5117+1578G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305441 | ||||||
| chr13:42305446
|
C | G | 2 | a0001c0001t0005g0073a0001c0001t0005g0074 | 2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.5117+1583C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305446 | ||||||
| chr13:42305566
|
G | A | 8 | a0001c0001t0020g0175a0001c0003t0010g0017a0001c0003t0010g0043others(5): Show | 10 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.5117+1703G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305566 | ||||||
| chr13:42305668
|
T | C | 5 | a0001c0001t0012g0007a0001c0001t0012g0118a0009c0011t0011g0117others(2): Show | 11 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.5117+1805T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305668 | ||||||
| chr13:42305868
|
A | T | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5117+2005A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305868 | ||||||
| chr13:42305902
|
G | A | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+2039G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305902 | ||||||
| chr13:42305919
|
G | A | 23 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(20): Show | 45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.5117+2056G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305919 | ||||||
| chr13:42306006
|
C | T | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5117+2143C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306006 | ||||||
| chr13:42306622
|
G | A | 1 | a0001c0001t0009g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5118-1832G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306622 | ||||||
| chr13:42306710
|
A | G | 1 | a0001c0001t0012g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5118-1744A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306710 | ||||||
| chr13:42306833
|
A | G | 15 | a0001c0001t0003g0195a0001c0001t0021g0005a0001c0001t0021g0030others(12): Show | 21 | HG00438.hp2 HG00609.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.5118-1621A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306833 | ||||||
| chr13:42306994
|
A | G | 1 | a0001c0001t0009g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5118-1460A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306994 | ||||||
| chr13:42307011
|
C | T | 1 | a0001c0001t0005g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5118-1443C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307011 | ||||||
| chr13:42307151
|
A | G | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5118-1303A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307151 | ||||||
| chr13:42307173
|
T | A | 5 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(2): Show | 14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5118-1281T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307173 | ||||||
| chr13:42307231
|
T | C | 11 | a0002c0004t0007g0122a0002c0004t0007g0131a0002c0004t0007g0134others(8): Show | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.5118-1223T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307231 | ||||||
| chr13:42307584
|
C | T | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5118-870C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307584 | ||||||
| chr13:42307665
|
G | T | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5118-789G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307665 | ||||||
| chr13:42307666
|
A | T | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5118-788A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307666 | ||||||
| chr13:42307772
|
C | T | 1 | a0001c0001t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5118-682C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307772 | ||||||
| chr13:42307791
|
T | TGGAA | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5118-660_5118-657d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 42307791 | |||||
| chr13:42307806
|
C | A | 256 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0036others(253): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.5118-648C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307806 | ||||||
| chr13:42308032
|
T | C | 1 | a0004c0009t0073g0174 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5118-422T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42308032 | ||||||
| chr13:42308251
|
G | A | 1 | a0008c0012t0034g0035 | 2 | HG01981.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5118-203G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42308251 | ||||||
| chr13:42308626
|
A | G | 211 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(208): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.5273+17A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308626 | ||||||
| chr13:42308902
|
A | AT | 116 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(113): Show | 153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5273+303dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42308902 | |||||
| chr13:42308902
|
A | T | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+293A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308902 | ||||||
| chr13:42308951
|
G | A | 1 | a0001c0001t0006g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5273+342G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308951 | ||||||
| chr13:42308976
|
G | C | 1 | a0001c0002t0017g0018 | 3 | NA18957.hp2 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5273+367G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308976 | ||||||
| chr13:42309004
|
A | G | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5273+395A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309004 | ||||||
| chr13:42309009
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5273+400A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309009 | ||||||
| chr13:42309037
|
G | A | 1 | a0001c0019t0081g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5273+428G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309037 | ||||||
| chr13:42309144
|
T | A | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5273+535T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309144 | ||||||
| chr13:42309149
|
C | CA | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.5273+542dupA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42309149 | |||||
| chr13:42309256
|
T | G | 1 | a0001c0001t0016g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5273+647T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309256 | ||||||
| chr13:42309318
|
G | A | 1 | a0001c0001t0028g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5273+709G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309318 | ||||||
| chr13:42309353
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+744G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309353 | ||||||
| chr13:42309630
|
A | G | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+1021A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309630 | ||||||
| chr13:42309674
|
G | A | 147 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(144): Show | 194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.5273+1065G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309674 | ||||||
| chr13:42310322
|
G | T | 1 | a0001c0001t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5273+1713G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310322 | ||||||
| chr13:42310333
|
A | G | 1 | a0001c0003t0010g0042 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5273+1724A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310333 | ||||||
| chr13:42310425
|
A | G | 3 | a0001c0001t0055g0189a0001c0001t0057g0190a0001c0001t0058g0188 | 3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5273+1816A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310425 | ||||||
| chr13:42310501
|
A | G | 2 | a0001c0002t0001g0027a0001c0026t0001g0027 | 2 | NA18945.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.5273+1892A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310501 | ||||||
| chr13:42310579
|
G | A | 1 | a0001c0002t0001g0028 | 2 | HG00597.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5273+1970G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310579 | ||||||
| chr13:42310590
|
C | T | 3 | a0004c0009t0072g0172a0004c0009t0073g0174a0004c0009t0080g0173 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5273+1981C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310590 | ||||||
| chr13:42310624
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+2015G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310624 | ||||||
| chr13:42310856
|
CA | C | 124 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(121): Show | 161 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.5274-2175delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42310856 | |||||
| chr13:42311006
|
A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5274-2041A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311006 | ||||||
| chr13:42311017
|
CTCTG | C | 119 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(116): Show | 156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5274-2024_5274-202 others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42311017 | |||||
| chr13:42311132
|
A | G | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.5274-1915A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311132 | ||||||
| chr13:42311425
|
A | G | 2 | a0011c0014t0022g0150a0011c0014t0022g0151 | 2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5274-1622A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311425 | ||||||
| chr13:42311541
|
G | A | 1 | a0001c0001t0013g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5274-1506G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311541 | ||||||
| chr13:42311835
|
A | G | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5274-1212A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311835 | ||||||
| chr13:42311916
|
A | G | 1 | a0001c0003t0025g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5274-1131A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311916 | ||||||
| chr13:42312029
|
A | C | 1 | a0001c0001t0009g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5274-1018A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312029 | ||||||
| chr13:42312099
|
T | C | 1 | a0001c0001t0005g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5274-948T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312099 | ||||||
| chr13:42312114
|
T | C | 1 | a0001c0001t0009g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5274-933T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312114 | ||||||
| chr13:42312311
|
G | A | 2 | a0007c0015t0013g0180a0007c0015t0028g0178 | 2 | HG01256.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5274-736G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312311 | ||||||
| chr13:42312595
|
A | G | 4 | a0001c0003t0025g0024a0001c0003t0025g0144a0001c0003t0025g0154others(1): Show | 6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.5274-452A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312595 | ||||||
| chr13:42312732
|
A | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5274-315A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312732 | ||||||
| chr13:42312832
|
C | T | 3 | a0001c0001t0006g0020a0001c0001t0014g0020a0001c0001t0070g0020 | 3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.5274-215C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312832 | ||||||
| chr13:42312875
|
A | G | 1 | a0001c0001t0006g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5274-172A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312875 | ||||||
| chr13:42312905
|
A | G | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5274-142A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312905 | ||||||
| chr13:42312909
|
C | T | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5274-138C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312909 | ||||||
| chr13:42312991
|
G | T | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5274-56G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312991 | ||||||
| chr13:42313001
|
A | G | 6 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(3): Show | 10 | HG01975.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.5274-46A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42313001 | ||||||
| chr13:42313277
|
C | A | 1 | a0023c0030t0084g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5357+147C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313277 | ||||||
| chr13:42313385
|
A | T | 1 | a0001c0001t0062g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5357+255A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313385 | ||||||
| chr13:42313430
|
G | C | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5357+300G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313430 | ||||||
| chr13:42313519
|
A | T | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5358-375A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313519 | ||||||
| chr13:42313820
|
T | C | 1 | a0001c0001t0002g0038 | 2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5358-74T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313820 | ||||||
| chr13:42313968
|
G | T | 1 | a0001c0002t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5404+28G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42313968 | ||||||
| chr13:42314094
|
A | G | 146 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(143): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.5404+154A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314094 | ||||||
| chr13:42314224
|
C | T | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+284C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314224 | ||||||
| chr13:42314274
|
A | G | 1 | a0001c0003t0010g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5404+334A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314274 | ||||||
| chr13:42314343
|
G | A | 7 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5404+403G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314343 | ||||||
| chr13:42314394
|
G | A | 3 | a0004c0009t0072g0172a0004c0009t0073g0174a0004c0009t0080g0173 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5404+454G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314394 | ||||||
| chr13:42314446
|
TAAAA | T | 13 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0111others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.5404+527_5404+530d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | |||||
| chr13:42314446
|
TAAAAA | T | 9 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0006g0103others(6): Show | 12 | HG00639.hp1 HG00733.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.5404+526_5404+530d others(7): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | |||||
| chr13:42314446
|
TAAAAAA | T | 139 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(136): Show | 198 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.5404+525_5404+530d others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | |||||
| chr13:42314446
|
TAAAAAAA | T | 23 | a0001c0003t0010g0017a0001c0003t0010g0023a0001c0003t0010g0042others(20): Show | 30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.5404+524_5404+530d others(9): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | |||||
| chr13:42314447
|
A | T | 1 | a0020c0024t0049g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5404+507A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314447 | ||||||
| chr13:42314798
|
T | A | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+858T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314798 | ||||||
| chr13:42314873
|
T | C | 3 | a0001c0001t0006g0034a0001c0001t0014g0105a0021c0016t0065g0034 | 3 | NA18951.hp1 NA18986.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.5404+933T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314873 | ||||||
| chr13:42314911
|
G | C | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5404+971G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314911 | ||||||
| chr13:42315127
|
A | T | 1 | a0015c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+1187A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315127 | ||||||
| chr13:42315186
|
A | C | 119 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(116): Show | 156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5404+1246A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315186 | ||||||
| chr13:42315496
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5404+1556C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315496 | ||||||
| chr13:42315543
|
TTAAC | T | 119 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(116): Show | 156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5404+1606_5404+160 others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42315543 | |||||
| chr13:42315622
|
T | G | 4 | a0001c0001t0002g0039a0001c0001t0002g0127a0001c0001t0036g0039others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.5404+1682T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315622 | ||||||
| chr13:42315639
|
C | T | 1 | a0005c0007t0039g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5404+1699C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315639 | ||||||
| chr13:42315642
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5404+1702G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315642 | ||||||
| chr13:42315938
|
A | G | 1 | a0001c0001t0013g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5405-1590A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315938 | ||||||
| chr13:42315962
|
C | T | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5405-1566C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315962 | ||||||
| chr13:42315973
|
G | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-1555G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315973 | ||||||
| chr13:42316137
|
G | A | 184 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(181): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.5405-1391G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316137 | ||||||
| chr13:42316187
|
T | G | 4 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(1): Show | 13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.5405-1341T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316187 | ||||||
| chr13:42316242
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-1286C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316242 | ||||||
| chr13:42316284
|
C | T | 1 | a0001c0001t0086g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5405-1244C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316284 | ||||||
| chr13:42316303
|
T | G | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5405-1225T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316303 | ||||||
| chr13:42316308
|
A | C | 1 | a0001c0019t0081g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5405-1220A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316308 | ||||||
| chr13:42316427
|
G | A | 1 | a0001c0001t0013g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5405-1101G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316427 | ||||||
| chr13:42316525
|
G | A | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5405-1003G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316525 | ||||||
| chr13:42316563
|
G | A | 6 | a0003c0005t0008g0006a0003c0005t0075g0063a0003c0022t0008g0198others(3): Show | 15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5405-965G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316563 | ||||||
| chr13:42316703
|
C | T | 1 | a0001c0001t0020g0084 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5405-825C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316703 | ||||||
| chr13:42316908
|
A | G | 37 | a0001c0001t0015g0014a0001c0001t0015g0109a0001c0001t0015g0110others(34): Show | 73 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.5405-620A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316908 | ||||||
| chr13:42317005
|
G | A | 3 | a0001c0001t0055g0189a0001c0001t0057g0190a0001c0001t0058g0188 | 3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5405-523G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317005 | ||||||
| chr13:42317013
|
G | C | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5405-515G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317013 | ||||||
| chr13:42317034
|
C | T | 30 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(27): Show | 61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.5405-494C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317034 | ||||||
| chr13:42317127
|
G | A | 1 | a0019c0017t0041g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5405-401G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317127 | ||||||
| chr13:42317130
|
G | A | 3 | a0005c0007t0034g0141a0005c0007t0039g0139a0005c0007t0039g0140 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5405-398G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317130 | ||||||
| chr13:42317260
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0027others(21): Show | 46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-268G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317260 | ||||||
| chr13:42317371
|
T | C | 1 | a0001c0001t0055g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5405-157T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317371 | ||||||
| chr13:42317452
|
G | T | 3 | a0001c0001t0020g0021a0001c0001t0067g0021a0001c0001t0069g0021 | 3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5405-76G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317452 | ||||||
| chr13:42317749
|
GTGATTGG others(10): Show |
G | 1 | a0001c0001t0035g0163 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5565+64_5565+80del others(17): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 42317749 | |||||
| chr13:42317777
|
T | A | 1 | a0001c0001t0021g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5565+89T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317777 | ||||||
| chr13:42317804
|
A | T | 3 | a0001c0003t0094g0156a0001c0003t0095g0152a0017c0020t0096g0153 | 3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5565+116A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317804 | ||||||
| chr13:42317919
|
C | T | 1 | a0001c0003t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5565+231C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317919 | ||||||
| chr13:42318339
|
A | T | 7 | a0001c0001t0003g0010a0001c0001t0003g0019a0001c0001t0006g0010others(4): Show | 10 | HG01928.hp2 HG03834.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.5565+651A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318339 | ||||||
| chr13:42318459
|
C | G | 1 | a0007c0015t0028g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5566-629C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318459 | ||||||
| chr13:42318557
|
G | GTATT | 8 | a0001c0001t0016g0157a0001c0001t0016g0159a0001c0001t0016g0160others(5): Show | 10 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.5566-513_5566-510d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 42318557 | |||||
| chr13:42318633
|
T | C | 1 | a0001c0001t0005g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5566-455T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318633 | ||||||
| chr13:42318667
|
C | A | 1 | a0004c0009t0080g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5566-421C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318667 | ||||||
| chr13:42318770
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5566-318G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318770 |