| geneid | 9465 |
|---|---|
| ensemblid | ENSG00000118507.19 |
| hgncid | 377 |
| symbol | AKAP7 |
| name | A-kinase anchoring protein 7 |
| refseq_nuc | NM_016377.4 |
| refseq_prot | NP_057461.2 |
| ensembl_nuc | ENST00000431975.7 |
| ensembl_prot | ENSP00000405252.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 131135467 |
| end | 131283532 |
| strand | + |
| ver | v1.2 |
| region | chr6:131135467-131283532 |
| region5000 | chr6:131130467-131288532 |
| regionname0 | AKAP7_chr6_131135467_131283532 |
| regionname5000 | AKAP7_chr6_131130467_131288532 |
| 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 | 348 | 223 | 51 | 31 | 114 | 7 | 18 | 99 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002 | 0/0 | 348 | 50 | 15 | 17 | 1 | 7 | 10 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003 | 0/0 | 348 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0004 | 0/0 | 348 | 7 | 0 | 5 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0005 | 0/0 | 348 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0006 | 0/0 | 348 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0007 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0008 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0009 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0010 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0011 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| 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 | 1047 | 223 | 51 | 31 | 114 | 7 | 18 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0002 | 0/0 | 1047 | 50 | 15 | 17 | 1 | 7 | 10 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0003 | 0/0 | 1047 | 10 | 10 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0004 | 0/0 | 1047 | 7 | 0 | 5 | 0 | 2 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0005 | 0/0 | 1047 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0006 | 0/0 | 1047 | 4 | 3 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0007 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0008 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0009 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0010 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| c0011 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| 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 | 1/1 | 2104 | 96 | 11 | 31 | 30 | 7 | 15 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0002 | 0/0 | 2104 | 49 | 3 | 7 | 29 | 3 | 7 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0003 | 0/0 | 2104 | 39 | 5 | 7 | 15 | 6 | 6 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0004 | 0/0 | 2102 | 27 | 0 | 2 | 25 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0005 | 0/0 | 2102 | 13 | 13 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0006 | 0/0 | 2102 | 10 | 0 | 1 | 9 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0007 | 0/0 | 2102 | 7 | 7 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0008 | 0/0 | 2101 | 7 | 7 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0009 | 0/0 | 2102 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0010 | 0/0 | 2101 | 4 | 3 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0011 | 0/0 | 2102 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0012 | 0/0 | 2102 | 3 | 0 | 2 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0013 | 0/0 | 2104 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0014 | 0/0 | 2113 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0015 | 0/0 | 2113 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0016 | 0/0 | 2113 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0017 | 0/0 | 2111 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0018 | 0/0 | 2117 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0019 | 0/0 | 2119 | 2 | 1 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0020 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0021 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0022 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0023 | 0/0 | 2101 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0024 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0025 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0026 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0027 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0028 | 0/0 | 2162 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0029 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0030 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0031 | 0/0 | 2101 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0032 | 0/0 | 2101 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0033 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0034 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0035 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0036 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0037 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0038 | 0/0 | 2104 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0039 | 0/0 | 2104 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0040 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0041 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| t0042 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| 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 | 1047 | 223 | 51 | 31 | 114 | 7 | 18 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002 | 0/0 | 1047 | 50 | 15 | 17 | 1 | 7 | 10 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003 | 0/0 | 1047 | 10 | 10 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0004c0004 | 0/0 | 1047 | 7 | 0 | 5 | 0 | 2 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0005c0005 | 0/0 | 1047 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0006c0006 | 0/0 | 1047 | 4 | 3 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0007c0011 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0008c0008 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0009c0009 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0010c0010 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0011c0007 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3150 | 69 | 7 | 19 | 29 | 1 | 11 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0002 | 0/0 | 3150 | 40 | 2 | 3 | 28 | 3 | 4 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0003 | 0/0 | 3150 | 27 | 4 | 2 | 15 | 3 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0004 | 0/0 | 3148 | 26 | 0 | 2 | 24 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0005 | 0/0 | 3148 | 9 | 9 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0006 | 0/0 | 3148 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0007 | 0/0 | 3148 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0008 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0009 | 0/0 | 3148 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0010 | 0/0 | 3147 | 3 | 2 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0011 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0012 | 0/0 | 3148 | 3 | 0 | 2 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0013 | 0/0 | 3150 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0016 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0018 | 0/0 | 3163 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0019 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0021 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0022 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0023 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0025 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0026 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0028 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0030 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0031 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0033 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0034 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0038 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0040 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0041 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0001c0001t0042 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0001 | 0/0 | 3150 | 22 | 4 | 8 | 1 | 5 | 4 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0002 | 0/0 | 3150 | 8 | 1 | 4 | 0 | 0 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0003 | 0/0 | 3150 | 10 | 1 | 4 | 0 | 2 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0015 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0017 | 0/0 | 3157 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0024 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0027 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0036 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0037 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0002c0002t0039 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003t0007 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003t0008 | 0/0 | 3147 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003t0010 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003t0019 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0003c0003t0032 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0004c0004t0001 | 0/0 | 3150 | 5 | 0 | 4 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0004c0004t0003 | 0/0 | 3150 | 2 | 0 | 1 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0005c0005t0005 | 0/0 | 3148 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0005c0005t0011 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0006c0006t0014 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0006c0006t0016 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0006c0006t0035 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0007c0011t0004 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0008c0008t0006 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0009c0009t0005 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0010c0010t0002 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| a0011c0007t0029 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | copy fasta | chr6 | 131130467 | 131288532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0016g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0018g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0020g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0021g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0022g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0023g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0025g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0026g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0028g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0030g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0031g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0033g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0038g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0040g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0041g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0042g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0020g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0024g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0027g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0036g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0037g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0039g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0032g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0016g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0035g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0007c0011t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0008c0008t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0009c0009t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0010c0010t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0011c0007t0029g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0216 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0248 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0182 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0113 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00323 | hp2 | a0004 | c0004 | t0003 | g0054 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00609 | hp2 | a0001 | c0001 | t0013 | g0111 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00741 | hp1 | a0001 | c0001 | t0038 | g0166 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01071 | hp2 | a0004 | c0004 | t0001 | g0001 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0001 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0235 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0070 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01255 | hp1 | a0004 | c0004 | t0001 | g0130 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0132 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0134 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01261 | hp2 | a0002 | c0002 | t0039 | g0079 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0108 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0270 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0114 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0135 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0136 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01884 | hp1 | a0002 | c0002 | t0015 | g0008 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0282 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01891 | hp1 | a0005 | c0005 | t0005 | g0098 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01891 | hp2 | a0003 | c0003 | t0032 | g0301 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0081 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0128 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01978 | hp2 | a0001 | c0001 | t0012 | g0057 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01993 | hp1 | a0004 | c0004 | t0003 | g0167 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02145 | hp2 | a0005 | c0005 | t0011 | g0165 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02155 | hp1 | a0001 | c0001 | t0042 | g0212 | EAS | CDX | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CDX | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02257 | hp1 | a0002 | c0002 | t0015 | g0009 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02257 | hp2 | a0002 | c0002 | t0036 | g0222 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02258 | hp1 | a0001 | c0001 | t0041 | g0158 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02258 | hp2 | a0009 | c0009 | t0005 | g0230 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02280 | hp2 | a0002 | c0002 | t0017 | g0007 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02300 | hp1 | a0001 | c0001 | t0012 | g0060 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0085 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0163 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0069 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0119 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02647 | hp1 | a0003 | c0003 | t0008 | g0147 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0185 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02717 | hp2 | a0005 | c0005 | t0005 | g0097 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02723 | hp1 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0116 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02809 | hp2 | a0002 | c0002 | t0017 | g0010 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0006 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02818 | hp2 | a0003 | c0003 | t0008 | g0144 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0218 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0101 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02897 | hp1 | a0001 | c0001 | t0033 | g0100 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0095 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02922 | hp2 | a0003 | c0003 | t0019 | g0242 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02970 | hp1 | a0003 | c0003 | t0008 | g0148 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03041 | hp2 | a0001 | c0001 | t0023 | g0175 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0174 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0302 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03130 | hp2 | a0001 | c0001 | t0040 | g0080 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0223 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03195 | hp1 | a0003 | c0003 | t0007 | g0228 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03195 | hp2 | a0002 | c0002 | t0024 | g0160 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03209 | hp2 | a0002 | c0002 | t0020 | g0149 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03225 | hp1 | a0003 | c0003 | t0008 | g0145 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03225 | hp2 | a0006 | c0006 | t0014 | g0004 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03453 | hp1 | a0002 | c0002 | t0027 | g0231 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03453 | hp2 | a0005 | c0005 | t0005 | g0099 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0050 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0048 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03516 | hp1 | a0011 | c0007 | t0029 | g0227 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03540 | hp1 | a0001 | c0001 | t0031 | g0285 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03540 | hp2 | a0003 | c0003 | t0008 | g0146 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0236 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0288 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0159 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | BEB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0220 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CHB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18906 | hp2 | a0006 | c0006 | t0014 | g0003 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0295 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0296 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18946 | hp1 | a0007 | c0011 | t0004 | g0198 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18969 | hp1 | a0001 | c0001 | t0013 | g0202 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0210 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18977 | hp2 | a0010 | c0010 | t0002 | g0249 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0061 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18981 | hp1 | a0008 | c0008 | t0006 | g0002 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18986 | hp2 | a0001 | c0001 | t0025 | g0066 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0290 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0291 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19043 | hp2 | a0002 | c0002 | t0037 | g0162 | AFR | LWK | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19083 | hp1 | a0001 | c0001 | t0018 | g0240 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19085 | hp1 | a0001 | c0001 | t0030 | g0294 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19087 | hp2 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19091 | hp1 | a0001 | c0001 | t0018 | g0241 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0086 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0122 | AFR | ASW | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20129 | hp2 | a0006 | c0006 | t0035 | g0217 | AFR | ASW | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | TSI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0137 | EUR | TSI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0233 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01123 | hp2 | a0006 | c0006 | t0016 | g0005 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02109 | hp1 | a0005 | c0005 | t0011 | g0139 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0251 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02559 | hp1 | a0003 | c0003 | t0010 | g0082 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG06807 | hp2 | a0003 | c0003 | t0008 | g0143 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131145341
|
G | A | 2 | a0006a0011 | 5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.76G>A | p.Glu26Lys | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/8 | 373/3150 | 76/1047 | 26/348 | chr6 | 131145341 | ||
| chr6:131145366
|
C | T | 1 | a0007 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.101C>T | p.Ser34Phe | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/8 | 398/3150 | 101/1047 | 34/348 | chr6 | 131145366 | ||
| chr6:131165133
|
G | A | 1 | a0008 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.344G>A | p.Arg115Gln | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/8 | 641/3150 | 344/1047 | 115/348 | chr6 | 131165133 | ||
| chr6:131165197
|
A | C | 1 | a0011 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.408A>C | p.Leu136Phe | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/8 | 705/3150 | 408/1047 | 136/348 | chr6 | 131165197 | ||
| chr6:131169123
|
G | T | 1 | a0003 | 10 | HG01891.hp2 HG02559.hp1 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.439G>T | p.Ala147Ser | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/8 | 736/3150 | 439/1047 | 147/348 | chr6 | 131169123 | ||
| chr6:131169171
|
C | T | 1 | a0010 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.487C>T | p.His163Tyr | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/8 | 784/3150 | 487/1047 | 163/348 | chr6 | 131169171 | ||
| chr6:131199502
|
G | C | 1 | a0005 | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
missense_variant | MODERATE | c.631G>C | p.Gly211Arg | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 928/3150 | 631/1047 | 211/348 | chr6 | 131199502 | ||
| chr6:131199515
|
G | A | 1 | a0002 | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
missense_variant | MODERATE | c.644G>A | p.Ser215Asn | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 941/3150 | 644/1047 | 215/348 | chr6 | 131199515 | ||
| chr6:131199551
|
A | G | 1 | a0004 | 7 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(4): Show |
missense_variant | MODERATE | c.680A>G | p.Lys227Arg | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 977/3150 | 680/1047 | 227/348 | chr6 | 131199551 | ||
| chr6:131219733
|
C | T | 1 | a0009 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.775C>T | p.Arg259Cys | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/8 | 1072/3150 | 775/1047 | 259/348 | chr6 | 131219733 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131135512
|
C | T | 1 | a0001c0001t0042 | 1 | HG02155.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | chr6 | 131135512 | ||||||
| chr6:131135513
|
T | C | 9 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(6): Show | 48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-251T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 251 | chr6 | 131135513 | |||||
| chr6:131135516
|
G | GGCTGCCG others(8): Show |
3 | a0001c0001t0018a0001c0001t0019a0003c0003t0019 | 4 | HG02922.hp2 NA19083.hp1 NA19087.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-239_-225dupCGCCGC others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 224 | INFO_REALIGN_3_PRIME | chr6 | 131135516 | ||||
| chr6:131135516
|
G | GGCTGCCG others(53): Show |
1 | a0001c0001t0028 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225_-224insCGCCGC others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 224 | INFO_REALIGN_3_PRIME | chr6 | 131135516 | ||||
| chr6:131135517
|
G | A | 1 | a0002c0002t0027 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-247G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 247 | chr6 | 131135517 | |||||
| chr6:131135529
|
G | GCTGCTGC others(2): Show |
5 | a0001c0001t0016a0002c0002t0015a0002c0002t0017others(2): Show | 8 | HG01123.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-227_-226insCCTGCT others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 226 | INFO_REALIGN_3_PRIME | chr6 | 131135529 | ||||
| chr6:131135593
|
G | C | 15 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(12): Show | 75 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(72): Show |
5_prime_UTR_variant | MODIFIER | c.-171G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 171 | chr6 | 131135593 | |||||
| chr6:131135639
|
G | C | 2 | a0001c0001t0020a0002c0002t0020 | 2 | HG02809.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-125G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 125 | chr6 | 131135639 | |||||
| chr6:131135722
|
G | A | 9 | a0001c0001t0008a0001c0001t0009a0001c0001t0021others(6): Show | 18 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 42 | chr6 | 131135722 | |||||
| chr6:131281804
|
C | T | 1 | a0002c0002t0037 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 78 | chr6 | 131281804 | |||||
| chr6:131281828
|
T | C | 4 | a0001c0001t0033a0001c0001t0038a0006c0006t0014others(1): Show | 5 | HG00741.hp1 HG02897.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*102T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 102 | chr6 | 131281828 | |||||
| chr6:131281939
|
T | C | 2 | a0001c0001t0021a0001c0001t0022 | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 213 | chr6 | 131281939 | |||||
| chr6:131281950
|
T | C | 3 | a0001c0001t0034a0002c0002t0015a0002c0002t0024 | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*224T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 224 | chr6 | 131281950 | |||||
| chr6:131281969
|
C | T | 4 | a0001c0001t0041a0002c0002t0017a0002c0002t0027others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 243 | chr6 | 131281969 | |||||
| chr6:131282226
|
AGT | A | 20 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(17): Show | 76 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*505delTG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 504 | INFO_REALIGN_3_PRIME | chr6 | 131282226 | ||||
| chr6:131282303
|
A | G | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0012others(3): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*577A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 577 | chr6 | 131282303 | |||||
| chr6:131282408
|
CTAT | C | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0023others(4): Show | 15 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*684_*686delATT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 684 | INFO_REALIGN_3_PRIME | chr6 | 131282408 | ||||
| chr6:131282802
|
A | G | 15 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(12): Show | 35 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1076A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1076 | chr6 | 131282802 | |||||
| chr6:131283137
|
A | T | 1 | a0001c0001t0026 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1411 | chr6 | 131283137 | |||||
| chr6:131283244
|
G | T | 1 | a0001c0001t0023 | 2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1518G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1518 | chr6 | 131283244 | |||||
| chr6:131283291
|
G | A | 3 | a0001c0001t0013a0001c0001t0025a0001c0001t0030 | 5 | HG00609.hp2 NA18969.hp1 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1565G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1565 | chr6 | 131283291 | |||||
| chr6:131283303
|
A | T | 1 | a0003c0003t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1577 | chr6 | 131283303 | |||||
| chr6:131283409
|
C | T | 1 | a0002c0002t0039 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1683 | chr6 | 131283409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131135842
|
C | T | 73 | a0001c0001t0002g0232a0001c0001t0002g0234a0001c0001t0002g0237others(70): Show | 73 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+60C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131135842 | ||||||
| chr6:131136155
|
T | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG00408.hp1 HG01074.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.19+373T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136155 | ||||||
| chr6:131136157
|
C | G | 3 | a0002c0002t0001g0229a0002c0002t0027g0231a0009c0009t0005g0230 | 3 | HG02055.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.19+375C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136157 | ||||||
| chr6:131136226
|
A | G | 2 | a0003c0003t0007g0228a0011c0007t0029g0227 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+444A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136226 | ||||||
| chr6:131136381
|
G | A | 8 | a0001c0001t0016g0006a0002c0002t0015g0008a0002c0002t0015g0009others(5): Show | 8 | HG01123.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+599G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136381 | ||||||
| chr6:131136517
|
A | G | 143 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(140): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.19+735A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136517 | ||||||
| chr6:131136597
|
G | A | 1 | a0001c0001t0007g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19+815G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136597 | ||||||
| chr6:131136645
|
T | G | 193 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.19+863T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136645 | ||||||
| chr6:131136806
|
T | TCAA | 3 | a0001c0001t0022g0095a0002c0002t0001g0096a0002c0002t0002g0244 | 3 | HG00741.hp2 HG01071.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.19+1024_19+1025ins others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136806 | ||||||
| chr6:131137137
|
A | AT | 11 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+1366dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137137 | |||||
| chr6:131137254
|
A | G | 62 | a0001c0001t0001g0161a0001c0001t0001g0187a0001c0001t0001g0188others(59): Show | 63 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.19+1472A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137254 | ||||||
| chr6:131137331
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19+1549G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137331 | ||||||
| chr6:131137381
|
TCTCTTTT others(26): Show |
T | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19+1604_19+1636del others(33): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137381 | |||||
| chr6:131137384
|
C | CT | 14 | a0001c0001t0001g0091a0001c0001t0005g0094a0001c0001t0010g0185others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+1616dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137384 | |||||
| chr6:131137386
|
T | C | 1 | a0001c0001t0004g0186 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.19+1604T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137386 | ||||||
| chr6:131137466
|
T | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+1684T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137466 | ||||||
| chr6:131137476
|
A | G | 1 | a0002c0002t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+1694A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137476 | ||||||
| chr6:131137487
|
A | G | 1 | a0002c0002t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.19+1705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137487 | ||||||
| chr6:131137499
|
C | T | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0005g0089others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+1717C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137499 | ||||||
| chr6:131137502
|
C | G | 5 | a0001c0001t0009g0184a0001c0001t0009g0221a0001c0001t0021g0220others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+1720C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137502 | ||||||
| chr6:131137842
|
A | G | 84 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(81): Show | 85 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.19+2060A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137842 | ||||||
| chr6:131137848
|
A | G | 29 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(26): Show | 29 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.19+2066A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137848 | ||||||
| chr6:131137945
|
C | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(8): Show | 11 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+2163C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137945 | ||||||
| chr6:131138046
|
T | C | 81 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.19+2264T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138046 | ||||||
| chr6:131138073
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19+2291A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138073 | ||||||
| chr6:131138108
|
C | A | 2 | a0001c0001t0005g0140a0001c0001t0009g0141 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.19+2326C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138108 | ||||||
| chr6:131138592
|
C | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.19+2810C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138592 | ||||||
| chr6:131138767
|
C | T | 57 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0125others(54): Show | 58 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.19+2985C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138767 | ||||||
| chr6:131138877
|
TA | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+3096delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138877 | ||||||
| chr6:131138907
|
T | C | 5 | a0006c0006t0014g0003a0006c0006t0014g0004a0006c0006t0016g0005others(2): Show | 5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3125T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138907 | ||||||
| chr6:131139445
|
C | G | 80 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(77): Show | 80 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.19+3663C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139445 | ||||||
| chr6:131139627
|
A | AGT | 81 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0151others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.19+3847_19+3848dup others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131139627 | |||||
| chr6:131139788
|
G | C | 137 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0083others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+4006G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139788 | ||||||
| chr6:131139794
|
T | C | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19+4012T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139794 | ||||||
| chr6:131139899
|
A | T | 5 | a0001c0001t0009g0184a0001c0001t0009g0221a0001c0001t0021g0220others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4117A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139899 | ||||||
| chr6:131139902
|
C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+4120C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139902 | ||||||
| chr6:131139976
|
ACT | A | 4 | a0001c0001t0001g0091a0001c0001t0005g0156a0001c0001t0041g0158others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4196_19+4197del others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131139976 | |||||
| chr6:131140063
|
C | G | 41 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(38): Show | 41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4281C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140063 | ||||||
| chr6:131140098
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.19+4316A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140098 | ||||||
| chr6:131140161
|
G | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+4379G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140161 | ||||||
| chr6:131140165
|
A | G | 41 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(38): Show | 41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4383A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140165 | ||||||
| chr6:131140174
|
A | T | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.19+4392A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140174 | ||||||
| chr6:131140198
|
C | T | 25 | a0001c0001t0001g0078a0001c0001t0007g0243a0001c0001t0007g0281others(22): Show | 25 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+4416C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140198 | ||||||
| chr6:131140266
|
A | AT | 14 | a0001c0001t0002g0297a0001c0001t0009g0184a0001c0001t0009g0221others(11): Show | 14 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.19+4496dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131140266 | |||||
| chr6:131140266
|
AT | A | 78 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(75): Show | 79 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.19+4496delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131140266 | |||||
| chr6:131140273
|
T | G | 2 | a0002c0002t0001g0229a0009c0009t0005g0230 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.19+4491T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140273 | ||||||
| chr6:131140331
|
G | A | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19+4549G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140331 | ||||||
| chr6:131140436
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.19+4654C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140436 | ||||||
| chr6:131140619
|
A | T | 5 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4666A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140619 | ||||||
| chr6:131140695
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.20-4590G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140695 | ||||||
| chr6:131140827
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0211a0001c0001t0042g0212 | 3 | HG02155.hp1 NA19001.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.20-4458A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140827 | ||||||
| chr6:131140844
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-4441A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140844 | ||||||
| chr6:131141014
|
G | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 8 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-4271G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141014 | ||||||
| chr6:131141070
|
CTTAA | C | 5 | a0006c0006t0014g0003a0006c0006t0014g0004a0006c0006t0016g0005others(2): Show | 5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4206_20-4203del others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141070 | |||||
| chr6:131141159
|
C | T | 27 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(24): Show | 27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.20-4126C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141159 | ||||||
| chr6:131141574
|
G | C | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.20-3711G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141574 | ||||||
| chr6:131141671
|
T | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(45): Show | 49 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.20-3614T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141671 | ||||||
| chr6:131141777
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.20-3508T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141777 | ||||||
| chr6:131141899
|
C | CT | 22 | a0001c0001t0001g0155a0001c0001t0002g0271a0001c0001t0002g0274others(19): Show | 22 | HG01256.hp1 HG02559.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-3367dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141899 | |||||
| chr6:131141899
|
CTT | C | 6 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-3368_20-3367del others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141899 | |||||
| chr6:131141902
|
T | TC | 44 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(41): Show | 44 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.20-3383_20-3382ins others(1): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141902 | ||||||
| chr6:131142213
|
C | T | 13 | a0001c0001t0002g0299a0001c0001t0007g0277a0001c0001t0038g0166others(10): Show | 14 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-3072C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142213 | ||||||
| chr6:131142284
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.20-3001C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142284 | ||||||
| chr6:131142291
|
A | G | 1 | a0002c0002t0003g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.20-2994A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142291 | ||||||
| chr6:131142416
|
G | T | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 176 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.20-2869G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142416 | ||||||
| chr6:131142448
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.20-2837A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142448 | ||||||
| chr6:131142451
|
G | T | 2 | a0002c0002t0003g0069a0002c0002t0003g0070 | 2 | HG01175.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.20-2834G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142451 | ||||||
| chr6:131142482
|
G | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 41 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-2803G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142482 | ||||||
| chr6:131142540
|
A | G | 2 | a0002c0002t0001g0229a0009c0009t0005g0230 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.20-2745A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142540 | ||||||
| chr6:131142615
|
C | T | 1 | a0002c0002t0003g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.20-2670C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142615 | ||||||
| chr6:131142800
|
G | C | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.20-2485G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142800 | ||||||
| chr6:131143229
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.20-2056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143229 | ||||||
| chr6:131143269
|
T | TA | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2014dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143269 | |||||
| chr6:131143525
|
T | G | 4 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0017g0010others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1760T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143525 | ||||||
| chr6:131143534
|
C | A | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-1751C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143534 | ||||||
| chr6:131143626
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-1659G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143626 | ||||||
| chr6:131143738
|
CT | C | 15 | a0001c0001t0001g0125a0001c0001t0001g0151a0001c0001t0002g0272others(12): Show | 16 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.20-1534delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143738 | |||||
| chr6:131143740
|
TTTTTTTT others(5): Show |
T | 4 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0181others(1): Show | 4 | HG00140.hp2 HG01074.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1538_20-1527del others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143740 | |||||
| chr6:131143745
|
T | A | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-1540T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143745 | ||||||
| chr6:131143745
|
T | TTA | 42 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0091others(39): Show | 42 | HG01074.hp1 HG01175.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-1539_20-1538ins others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143745 | |||||
| chr6:131143752
|
A | T | 1 | a0002c0002t0003g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.20-1533A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143752 | ||||||
| chr6:131143759
|
A | T | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20-1526A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143759 | ||||||
| chr6:131143805
|
G | A | 1 | a0001c0001t0021g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.20-1480G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143805 | ||||||
| chr6:131143902
|
C | G | 1 | a0002c0002t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.20-1383C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143902 | ||||||
| chr6:131143905
|
G | GCGGCCTT others(1): Show |
80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0028others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.20-1377_20-1370dup others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143905 | |||||
| chr6:131143906
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0013g0210 | 2 | NA18955.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.20-1379C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143906 | ||||||
| chr6:131143913
|
C | T | 4 | a0002c0002t0002g0302a0003c0003t0007g0228a0003c0003t0019g0242others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-1372C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143913 | ||||||
| chr6:131144290
|
C | G | 22 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0003g0142others(19): Show | 23 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-995C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144290 | ||||||
| chr6:131144609
|
T | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-676T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144609 | ||||||
| chr6:131144609
|
T | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.20-676T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144609 | ||||||
| chr6:131144610
|
T | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-675T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144610 | ||||||
| chr6:131144848
|
G | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-437G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144848 | ||||||
| chr6:131145105
|
TAG | T | 5 | a0006c0006t0014g0003a0006c0006t0014g0004a0006c0006t0016g0005others(2): Show | 5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-177_20-176delAG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131145105 | |||||
| chr6:131145256
|
C | A | 2 | a0001c0001t0002g0292a0001c0001t0004g0026 | 2 | HG01943.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.20-29C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131145256 | ||||||
| chr6:131145656
|
A | G | 2 | a0001c0001t0007g0277a0001c0001t0008g0218 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.151+240A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145656 | ||||||
| chr6:131145848
|
C | T | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+432C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145848 | ||||||
| chr6:131145918
|
A | C | 48 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(45): Show | 48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.151+502A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145918 | ||||||
| chr6:131145967
|
G | C | 174 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(171): Show | 175 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.151+551G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145967 | ||||||
| chr6:131146094
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151+678C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146094 | ||||||
| chr6:131146466
|
A | T | 3 | a0001c0001t0005g0224a0001c0001t0007g0281a0001c0001t0007g0282 | 3 | HG01884.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.151+1050A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146466 | ||||||
| chr6:131146608
|
A | T | 5 | a0001c0001t0002g0299a0001c0001t0038g0166a0004c0004t0001g0001others(2): Show | 6 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+1192A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146608 | ||||||
| chr6:131146657
|
G | T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.151+1241G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146657 | ||||||
| chr6:131146813
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+1397A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146813 | ||||||
| chr6:131147018
|
T | G | 122 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(119): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.151+1602T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147018 | ||||||
| chr6:131147361
|
G | A | 17 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(14): Show | 17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.151+1945G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147361 | ||||||
| chr6:131147395
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.151+1979C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147395 | ||||||
| chr6:131147461
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0043 | 2 | NA18977.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.151+2045G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147461 | ||||||
| chr6:131147937
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.151+2521C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147937 | ||||||
| chr6:131148008
|
T | C | 8 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+2592T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148008 | ||||||
| chr6:131148089
|
C | T | 2 | a0001c0001t0005g0140a0001c0001t0009g0141 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+2673C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148089 | ||||||
| chr6:131148312
|
G | T | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151+2896G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148312 | ||||||
| chr6:131148321
|
G | T | 178 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.151+2905G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148321 | ||||||
| chr6:131148344
|
A | G | 6 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+2928A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148344 | ||||||
| chr6:131148471
|
T | C | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.151+3055T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148471 | ||||||
| chr6:131148471
|
TC | T | 149 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(146): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.151+3064delC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148471 | |||||
| chr6:131148471
|
TCC | T | 26 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(23): Show | 26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+3063_151+3064d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148471 | |||||
| chr6:131148586
|
C | T | 2 | a0001c0001t0002g0269a0001c0001t0002g0270 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.151+3170C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148586 | ||||||
| chr6:131148713
|
G | T | 1 | a0001c0001t0010g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.151+3297G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148713 | ||||||
| chr6:131148765
|
C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151+3349C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148765 | ||||||
| chr6:131148943
|
CT | C | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+3530delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148943 | |||||
| chr6:131149096
|
C | T | 82 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0028others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.151+3680C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149096 | ||||||
| chr6:131149393
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.151+3977G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149393 | ||||||
| chr6:131149401
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+3985G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149401 | ||||||
| chr6:131149517
|
C | T | 48 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(45): Show | 48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.151+4101C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149517 | ||||||
| chr6:131149615
|
A | T | 5 | a0001c0001t0001g0170a0001c0001t0002g0237a0002c0002t0001g0096others(2): Show | 5 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+4199A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149615 | ||||||
| chr6:131149699
|
T | C | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+4283T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149699 | ||||||
| chr6:131149709
|
A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151+4293A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149709 | ||||||
| chr6:131150053
|
C | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+4637C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150053 | ||||||
| chr6:131150154
|
T | C | 1 | a0005c0005t0011g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.151+4738T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150154 | ||||||
| chr6:131150172
|
C | A | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.151+4756C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150172 | ||||||
| chr6:131150252
|
G | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(23): Show | 26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+4836G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150252 | ||||||
| chr6:131150769
|
T | C | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.151+5353T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150769 | ||||||
| chr6:131151008
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+5592A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151008 | ||||||
| chr6:131151165
|
C | T | 6 | a0002c0002t0001g0157a0006c0006t0014g0003a0006c0006t0014g0004others(3): Show | 6 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5749C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151165 | ||||||
| chr6:131151249
|
G | A | 1 | a0006c0006t0016g0005 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.151+5833G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151249 | ||||||
| chr6:131151381
|
G | GT | 21 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(18): Show | 22 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+5979dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | |||||
| chr6:131151381
|
G | GTT | 29 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(26): Show | 29 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.151+5978_151+5979d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | |||||
| chr6:131151381
|
G | GTTT | 6 | a0001c0001t0001g0088a0002c0002t0001g0093a0002c0002t0015g0008others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5977_151+5979d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | |||||
| chr6:131151583
|
A | G | 9 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 9 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+6167A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151583 | ||||||
| chr6:131151904
|
A | G | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+6488A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151904 | ||||||
| chr6:131152032
|
C | T | 8 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+6616C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152032 | ||||||
| chr6:131152089
|
G | GC | 26 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(23): Show | 26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+6674dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152089 | |||||
| chr6:131152221
|
T | C | 9 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 9 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+6805T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152221 | ||||||
| chr6:131152461
|
A | G | 4 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0017g0010others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+7045A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152461 | ||||||
| chr6:131152622
|
G | A | 2 | a0001c0001t0001g0078a0002c0002t0001g0133 | 2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.151+7206G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152622 | ||||||
| chr6:131152660
|
C | G | 1 | a0001c0001t0003g0043 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.151+7244C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152660 | ||||||
| chr6:131152689
|
A | T | 172 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(169): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.151+7273A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152689 | ||||||
| chr6:131152738
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-7321A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152738 | ||||||
| chr6:131152826
|
C | CA | 14 | a0001c0001t0001g0084a0001c0001t0001g0125a0001c0001t0001g0152others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-7213dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152826 | |||||
| chr6:131152858
|
C | G | 173 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.152-7201C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152858 | ||||||
| chr6:131152935
|
TG | T | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-7122delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152935 | |||||
| chr6:131152998
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.152-7061C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152998 | ||||||
| chr6:131153077
|
C | T | 1 | a0001c0001t0003g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152-6982C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153077 | ||||||
| chr6:131153107
|
A | G | 1 | a0002c0002t0001g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152-6952A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153107 | ||||||
| chr6:131153108
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152-6951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153108 | ||||||
| chr6:131153129
|
C | CA | 9 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01891.hp1 HG01978.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-6915dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | |||||
| chr6:131153129
|
C | CAA | 29 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(26): Show | 30 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.152-6916_152-6915d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | |||||
| chr6:131153129
|
C | CAAA | 19 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0007g0277others(16): Show | 19 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-6917_152-6915d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | |||||
| chr6:131153406
|
A | G | 56 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.152-6653A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153406 | ||||||
| chr6:131153621
|
G | T | 5 | a0001c0001t0010g0081a0002c0002t0002g0302a0003c0003t0007g0228others(2): Show | 5 | HG01891.hp2 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-6438G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153621 | ||||||
| chr6:131153670
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-6389G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153670 | ||||||
| chr6:131153755
|
ATATCT | A | 3 | a0001c0001t0004g0208a0001c0001t0004g0209a0001c0001t0006g0296 | 3 | HG00597.hp1 NA18943.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.152-6297_152-6293d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153755 | |||||
| chr6:131153935
|
TGTG | T | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-6119_152-6117d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153935 | |||||
| chr6:131154041
|
C | G | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.152-6018C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154041 | ||||||
| chr6:131154090
|
T | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(187): Show | 190 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.152-5969T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154090 | ||||||
| chr6:131154112
|
G | A | 27 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(24): Show | 27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-5947G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154112 | ||||||
| chr6:131154179
|
G | C | 10 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-5880G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154179 | ||||||
| chr6:131154211
|
A | AC | 4 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0017g0010others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-5848_152-5847i others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154211 | ||||||
| chr6:131154212
|
A | C | 40 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(37): Show | 40 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-5847A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154212 | ||||||
| chr6:131154369
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.152-5690C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154369 | ||||||
| chr6:131154468
|
G | GT | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0034others(12): Show | 15 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-5569dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | |||||
| chr6:131154468
|
GT | G | 86 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0126others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.152-5569delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | |||||
| chr6:131154468
|
GTT | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(37): Show | 40 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-5570_152-5569d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | |||||
| chr6:131154468
|
GTTT | G | 6 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-5571_152-5569d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | |||||
| chr6:131154513
|
G | C | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-5546G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154513 | ||||||
| chr6:131154627
|
T | A | 1 | a0001c0001t0003g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.152-5432T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154627 | ||||||
| chr6:131154802
|
C | A | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-5257C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154802 | ||||||
| chr6:131154866
|
A | G | 23 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0010g0081others(20): Show | 23 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-5193A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154866 | ||||||
| chr6:131154951
|
T | G | 8 | a0001c0001t0003g0124a0001c0001t0009g0184a0001c0001t0009g0221others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-5108T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154951 | ||||||
| chr6:131155019
|
AT | A | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.152-5028delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131155019 | |||||
| chr6:131155109
|
A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152-4950A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155109 | ||||||
| chr6:131155149
|
G | A | 1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-4910G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155149 | ||||||
| chr6:131155259
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152-4800C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155259 | ||||||
| chr6:131155379
|
C | G | 2 | a0002c0002t0001g0229a0009c0009t0005g0230 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.152-4680C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155379 | ||||||
| chr6:131155388
|
A | G | 27 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(24): Show | 27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-4671A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155388 | ||||||
| chr6:131155445
|
G | A | 1 | a0001c0001t0006g0290 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.152-4614G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155445 | ||||||
| chr6:131155790
|
C | T | 48 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(45): Show | 48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.152-4269C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155790 | ||||||
| chr6:131156118
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-3941C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156118 | ||||||
| chr6:131156132
|
T | C | 17 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(14): Show | 17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-3927T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156132 | ||||||
| chr6:131156589
|
A | G | 40 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-3470A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156589 | ||||||
| chr6:131157017
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-3042C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157017 | ||||||
| chr6:131157022
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-3037G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157022 | ||||||
| chr6:131157055
|
A | G | 1 | a0001c0001t0012g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-3004A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157055 | ||||||
| chr6:131157065
|
A | G | 1 | a0001c0001t0012g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-2994A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157065 | ||||||
| chr6:131157068
|
C | T | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152-2991C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157068 | ||||||
| chr6:131157113
|
T | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-2946T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157113 | ||||||
| chr6:131157244
|
G | A | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152-2815G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157244 | ||||||
| chr6:131157298
|
T | C | 21 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-2761T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157298 | ||||||
| chr6:131157420
|
A | G | 1 | a0001c0001t0004g0195 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-2639A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157420 | ||||||
| chr6:131157448
|
G | A | 138 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(135): Show | 138 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.152-2611G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157448 | ||||||
| chr6:131157486
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-2573A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157486 | ||||||
| chr6:131157596
|
C | G | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-2463C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157596 | ||||||
| chr6:131157668
|
A | G | 3 | a0001c0001t0004g0195a0001c0001t0018g0240a0001c0001t0018g0241 | 3 | NA18973.hp2 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.152-2391A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157668 | ||||||
| chr6:131157680
|
A | G | 16 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(13): Show | 16 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-2379A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157680 | ||||||
| chr6:131157686
|
A | T | 5 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-2373A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157686 | ||||||
| chr6:131157697
|
A | G | 4 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0017g0010others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-2362A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157697 | ||||||
| chr6:131158033
|
C | T | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152-2026C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158033 | ||||||
| chr6:131158189
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.152-1870A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158189 | ||||||
| chr6:131158327
|
CCTT | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0003g0073 | 3 | HG02602.hp2 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152-1728_152-1726d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158327 | |||||
| chr6:131158474
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.152-1585T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158474 | ||||||
| chr6:131158610
|
C | T | 17 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(14): Show | 17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-1449C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158610 | ||||||
| chr6:131158652
|
T | A | 27 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(24): Show | 27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-1407T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158652 | ||||||
| chr6:131158804
|
G | T | 1 | a0001c0001t0003g0056 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.152-1255G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158804 | ||||||
| chr6:131158915
|
T | TA | 50 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(47): Show | 50 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.152-1130dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158915 | |||||
| chr6:131158915
|
TA | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 41 | HG00741.hp1 HG01081.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.152-1130delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158915 | |||||
| chr6:131159047
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-1012C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159047 | ||||||
| chr6:131159087
|
ATTTTATT | A | 148 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.152-954_152-948del others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131159087 | |||||
| chr6:131159117
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-942G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159117 | ||||||
| chr6:131159125
|
C | A | 18 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(15): Show | 18 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-934C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159125 | ||||||
| chr6:131159132
|
C | T | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.152-927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159132 | ||||||
| chr6:131159194
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.152-865T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159194 | ||||||
| chr6:131159279
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.152-780G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159279 | ||||||
| chr6:131159283
|
C | T | 3 | a0002c0002t0001g0181a0002c0002t0001g0182a0002c0002t0002g0235 | 3 | HG00140.hp2 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.152-776C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159283 | ||||||
| chr6:131159295
|
G | A | 3 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0024g0160 | 3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.152-764G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159295 | ||||||
| chr6:131159299
|
T | C | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-760T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159299 | ||||||
| chr6:131159329
|
G | A | 1 | a0001c0001t0007g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152-730G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159329 | ||||||
| chr6:131159339
|
C | T | 46 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(43): Show | 46 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-720C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159339 | ||||||
| chr6:131159340
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-719G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159340 | ||||||
| chr6:131159354
|
A | G | 5 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159354 | ||||||
| chr6:131159367
|
A | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-692A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159367 | ||||||
| chr6:131159396
|
G | T | 93 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0028others(90): Show | 93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-663G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159396 | ||||||
| chr6:131159407
|
A | T | 9 | a0001c0001t0001g0155a0001c0001t0001g0164a0001c0001t0001g0225others(6): Show | 9 | HG01256.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-652A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159407 | ||||||
| chr6:131159433
|
A | G | 32 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 32 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.152-626A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159433 | ||||||
| chr6:131159859
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.152-200T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159859 | ||||||
| chr6:131159990
|
G | GT | 40 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0087others(37): Show | 40 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-60dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131159990 | |||||
| chr6:131160254
|
CA | C | 254 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.291+58delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131160254 | |||||
| chr6:131160443
|
G | T | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+245G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160443 | ||||||
| chr6:131160516
|
C | T | 41 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(38): Show | 41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+318C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160516 | ||||||
| chr6:131160530
|
C | T | 101 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0028others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.291+332C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160530 | ||||||
| chr6:131160699
|
G | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.291+501G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160699 | ||||||
| chr6:131160903
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0005g0156a0001c0001t0041g0158 | 3 | HG02258.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.291+705C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160903 | ||||||
| chr6:131160918
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.291+720A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160918 | ||||||
| chr6:131160987
|
T | C | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.291+789T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160987 | ||||||
| chr6:131160996
|
A | AT | 256 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.291+800dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131160996 | |||||
| chr6:131161000
|
C | T | 41 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(38): Show | 41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+802C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161000 | ||||||
| chr6:131161149
|
A | C | 101 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0028others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.291+951A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161149 | ||||||
| chr6:131161601
|
T | C | 253 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.291+1403T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161601 | ||||||
| chr6:131161613
|
C | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(28): Show | 31 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.291+1415C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161613 | ||||||
| chr6:131161644
|
C | CA | 20 | a0001c0001t0001g0012a0001c0001t0001g0123a0001c0001t0001g0126others(17): Show | 21 | HG00099.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.291+1486dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAA | 25 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(22): Show | 25 | HG00544.hp2 HG01081.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+1485_291+1486d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAA | 12 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0179others(9): Show | 12 | HG01943.hp2 HG02155.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+1484_291+1486d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAA | 13 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0088others(10): Show | 13 | HG00408.hp2 HG01109.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.291+1483_291+1486d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAAAAA | 6 | a0001c0001t0002g0300a0001c0001t0003g0077a0001c0001t0003g0150others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+1480_291+1486d others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0094a0001c0001t0011g0163 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.291+1477_291+1486d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.291+1475_291+1486d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0154others(3): Show | 6 | HG01106.hp1 HG01192.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+1474_291+1486d others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0225 | 2 | HG01099.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.291+1473_291+1486d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CA | C | 8 | a0001c0001t0003g0049a0001c0001t0003g0053a0001c0001t0007g0277others(5): Show | 8 | HG00280.hp1 HG00323.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+1486delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAA | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0131others(12): Show | 15 | HG00408.hp1 HG00597.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.291+1483_291+1486d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAA | C | 43 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(40): Show | 43 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.291+1482_291+1486d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAA | C | 36 | a0001c0001t0001g0015a0001c0001t0001g0104a0001c0001t0001g0110others(33): Show | 36 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.291+1481_291+1486d others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(3): Show |
C | 30 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0003g0051others(27): Show | 30 | HG01074.hp1 HG01074.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.291+1477_291+1486d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0182 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.291+1476_291+1486d others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0052a0002c0002t0003g0119 | 2 | HG00099.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.291+1475_291+1486d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(8): Show |
C | 2 | a0002c0002t0001g0229a0009c0009t0005g0230 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.291+1472_291+1486d others(17): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0004g0033a0001c0001t0004g0035a0001c0001t0006g0284 | 3 | NA18970.hp1 NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.291+1471_291+1486d others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(10): Show |
C | 16 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0004g0038others(13): Show | 16 | HG00597.hp1 HG01884.hp2 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+1470_291+1486d others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0004g0039 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.291+1469_291+1486d others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161644
|
CAAAAAAA others(14): Show |
C | 4 | a0001c0001t0001g0078a0005c0005t0005g0097a0005c0005t0005g0098others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+1466_291+1486d others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | |||||
| chr6:131161866
|
A | G | 1 | a0001c0001t0012g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.291+1668A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161866 | ||||||
| chr6:131162143
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0002g0264 | 2 | HG00609.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.291+1945C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162143 | ||||||
| chr6:131162528
|
T | C | 3 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0007g0286 | 3 | HG02622.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.291+2330T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162528 | ||||||
| chr6:131162529
|
A | G | 1 | a0002c0002t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+2331A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162529 | ||||||
| chr6:131162569
|
A | T | 1 | a0002c0002t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+2371A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162569 | ||||||
| chr6:131162638
|
G | A | 102 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.291+2440G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162638 | ||||||
| chr6:131162699
|
C | T | 42 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(39): Show | 42 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.292-2382C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162699 | ||||||
| chr6:131162978
|
C | T | 1 | a0001c0001t0005g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.292-2103C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162978 | ||||||
| chr6:131163005
|
G | GCT | 101 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.292-2061_292-2060d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163005 | |||||
| chr6:131163210
|
G | GTAATGTT others(26): Show |
1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.292-1866_292-1834d others(35): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163210 | |||||
| chr6:131163739
|
T | A | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.292-1342T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163739 | ||||||
| chr6:131163789
|
TG | T | 3 | a0004c0004t0001g0001a0004c0004t0001g0216a0004c0004t0003g0167 | 4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1287delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163789 | |||||
| chr6:131163836
|
GA | G | 3 | a0001c0001t0007g0243a0001c0001t0021g0223a0002c0002t0001g0093 | 3 | HG02615.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.292-1244delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163836 | ||||||
| chr6:131163901
|
C | T | 6 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1180C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163901 | ||||||
| chr6:131163964
|
G | A | 110 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(107): Show | 110 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.292-1117G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163964 | ||||||
| chr6:131164203
|
T | C | 8 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 8 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-878T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164203 | ||||||
| chr6:131164267
|
T | C | 6 | a0001c0001t0038g0166a0004c0004t0001g0001a0004c0004t0001g0128others(3): Show | 7 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-814T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164267 | ||||||
| chr6:131164480
|
T | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0178others(1): Show | 4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-601T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164480 | ||||||
| chr6:131164621
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292-460A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164621 | ||||||
| chr6:131164692
|
G | T | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292-389G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164692 | ||||||
| chr6:131164901
|
C | G | 27 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.292-180C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164901 | ||||||
| chr6:131165253
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.428+36A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165253 | ||||||
| chr6:131165326
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.428+109T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165326 | ||||||
| chr6:131165528
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.428+311C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165528 | ||||||
| chr6:131165563
|
A | G | 1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428+346A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165563 | ||||||
| chr6:131165571
|
TC | T | 4 | a0002c0002t0027g0231a0005c0005t0005g0097a0005c0005t0005g0098others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+355delC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165571 | ||||||
| chr6:131165733
|
C | G | 1 | a0001c0001t0012g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.428+516C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165733 | ||||||
| chr6:131165808
|
A | G | 15 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(12): Show | 15 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.428+591A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165808 | ||||||
| chr6:131165894
|
T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428+677T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165894 | ||||||
| chr6:131166177
|
G | A | 1 | a0001c0001t0012g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.428+960G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166177 | ||||||
| chr6:131166365
|
C | CTG | 6 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0153others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+1156_428+1157d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131166365 | |||||
| chr6:131166373
|
G | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0078others(38): Show | 41 | HG00140.hp2 HG00408.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.428+1156G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166373 | ||||||
| chr6:131166374
|
T | G | 41 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0078others(38): Show | 41 | HG00140.hp2 HG00408.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.428+1157T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166374 | ||||||
| chr6:131166543
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0131 | 2 | NA18965.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.428+1326G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166543 | ||||||
| chr6:131166585
|
C | A | 2 | a0001c0001t0005g0076a0002c0002t0027g0231 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.428+1368C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166585 | ||||||
| chr6:131166953
|
T | TA | 102 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.428+1743dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131166953 | |||||
| chr6:131166996
|
G | A | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428+1779G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166996 | ||||||
| chr6:131167375
|
G | A | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429-1738G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167375 | ||||||
| chr6:131167455
|
T | C | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.429-1658T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167455 | ||||||
| chr6:131167702
|
C | T | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.429-1411C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167702 | ||||||
| chr6:131167960
|
G | A | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.429-1153G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167960 | ||||||
| chr6:131168077
|
G | A | 2 | a0002c0002t0001g0121a0011c0007t0029g0227 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.429-1036G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168077 | ||||||
| chr6:131168096
|
T | C | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.429-1017T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168096 | ||||||
| chr6:131168201
|
T | C | 226 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(223): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.429-912T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168201 | ||||||
| chr6:131168223
|
A | G | 256 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(253): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.429-890A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168223 | ||||||
| chr6:131168272
|
A | G | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-841A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168272 | ||||||
| chr6:131168426
|
GA | G | 14 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(11): Show | 14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.429-686delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168426 | ||||||
| chr6:131168550
|
T | C | 128 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.429-563T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168550 | ||||||
| chr6:131168616
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.429-497G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168616 | ||||||
| chr6:131168875
|
C | CT | 4 | a0002c0002t0020g0149a0005c0005t0005g0097a0005c0005t0005g0098others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-235dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131168875 | |||||
| chr6:131169052
|
AT | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-58delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131169052 | |||||
| chr6:131169089
|
GA | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0164others(18): Show | 21 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.429-19delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131169089 | |||||
| chr6:131169332
|
T | C | 154 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.589+59T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169332 | ||||||
| chr6:131169391
|
T | G | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.589+118T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169391 | ||||||
| chr6:131169403
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.589+130G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169403 | ||||||
| chr6:131169407
|
C | A | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589+134C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169407 | ||||||
| chr6:131169440
|
A | C | 4 | a0001c0001t0007g0277a0002c0002t0015g0008a0002c0002t0015g0009others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+167A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169440 | ||||||
| chr6:131169447
|
T | A | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+174T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169447 | ||||||
| chr6:131169482
|
A | G | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+209A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169482 | ||||||
| chr6:131169806
|
T | TA | 4 | a0002c0002t0020g0149a0005c0005t0005g0097a0005c0005t0005g0098others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+534dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131169806 | |||||
| chr6:131169900
|
A | G | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.589+627A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169900 | ||||||
| chr6:131169904
|
G | A | 1 | a0001c0001t0010g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.589+631G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169904 | ||||||
| chr6:131170095
|
A | C | 1 | a0001c0001t0003g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.589+822A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170095 | ||||||
| chr6:131170152
|
T | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+879T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170152 | ||||||
| chr6:131170153
|
G | C | 38 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(35): Show | 38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+880G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170153 | ||||||
| chr6:131170183
|
A | T | 154 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.589+910A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170183 | ||||||
| chr6:131170290
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0178others(1): Show | 4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+1017A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170290 | ||||||
| chr6:131170300
|
A | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0153others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+1027A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170300 | ||||||
| chr6:131170308
|
AAG | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(17): Show | 20 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.589+1037_589+1038d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170308 | |||||
| chr6:131170310
|
GA | G | 206 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(203): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.589+1047delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170310 | |||||
| chr6:131170311
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(17): Show | 20 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.589+1038A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170311 | ||||||
| chr6:131170334
|
A | G | 38 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(35): Show | 38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+1061A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170334 | ||||||
| chr6:131170367
|
GA | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+1104delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170367 | |||||
| chr6:131170428
|
A | C | 1 | a0001c0001t0003g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.589+1155A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170428 | ||||||
| chr6:131170441
|
T | G | 2 | a0001c0001t0006g0002a0008c0008t0006g0002 | 2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.589+1168T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170441 | ||||||
| chr6:131170711
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0002g0267a0001c0001t0002g0275 | 3 | HG00544.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.589+1438T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170711 | ||||||
| chr6:131170963
|
G | A | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.589+1690G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170963 | ||||||
| chr6:131171177
|
G | T | 3 | a0002c0002t0001g0067a0002c0002t0001g0120a0002c0002t0002g0288 | 3 | HG03669.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.589+1904G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171177 | ||||||
| chr6:131171218
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.589+1945A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171218 | ||||||
| chr6:131171323
|
T | C | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+2050T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171323 | ||||||
| chr6:131171604
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0178others(1): Show | 4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+2331G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171604 | ||||||
| chr6:131171608
|
T | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+2335T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171608 | ||||||
| chr6:131171725
|
A | C | 50 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.589+2452A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171725 | ||||||
| chr6:131171823
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.589+2550T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171823 | ||||||
| chr6:131172063
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.589+2790G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172063 | ||||||
| chr6:131172078
|
A | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 56 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.589+2805A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172078 | ||||||
| chr6:131172109
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.589+2836C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172109 | ||||||
| chr6:131172206
|
A | G | 153 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.589+2933A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172206 | ||||||
| chr6:131172229
|
T | C | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+2956T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172229 | ||||||
| chr6:131172269
|
C | T | 11 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0088others(8): Show | 11 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+2996C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172269 | ||||||
| chr6:131172283
|
G | A | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.589+3010G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172283 | ||||||
| chr6:131172351
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0225a0001c0001t0005g0094others(3): Show | 6 | HG01952.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+3078T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172351 | ||||||
| chr6:131172510
|
A | C | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(152): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.589+3237A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172510 | ||||||
| chr6:131172638
|
T | C | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+3365T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172638 | ||||||
| chr6:131172654
|
A | C | 2 | a0003c0003t0008g0147a0003c0003t0008g0148 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.589+3381A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172654 | ||||||
| chr6:131172781
|
T | C | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+3508T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172781 | ||||||
| chr6:131172962
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.589+3689C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172962 | ||||||
| chr6:131173076
|
C | A | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+3803C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173076 | ||||||
| chr6:131173126
|
G | A | 8 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+3853G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173126 | ||||||
| chr6:131173133
|
G | A | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+3860G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173133 | ||||||
| chr6:131173155
|
C | T | 128 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.589+3882C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173155 | ||||||
| chr6:131173200
|
CA | C | 169 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.589+3943delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131173200 | |||||
| chr6:131173300
|
A | G | 2 | a0001c0001t0007g0251a0001c0001t0009g0101 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.589+4027A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173300 | ||||||
| chr6:131173301
|
T | A | 14 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(11): Show | 14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.589+4028T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173301 | ||||||
| chr6:131173326
|
T | C | 14 | a0001c0001t0002g0300a0001c0001t0003g0142a0001c0001t0003g0150others(11): Show | 14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.589+4053T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173326 | ||||||
| chr6:131173339
|
C | A | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.589+4066C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173339 | ||||||
| chr6:131173376
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.589+4103A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173376 | ||||||
| chr6:131173772
|
C | CTTAG | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+4500_589+4503d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131173772 | |||||
| chr6:131174028
|
T | C | 1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.589+4755T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174028 | ||||||
| chr6:131174175
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.589+4902T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174175 | ||||||
| chr6:131174360
|
T | C | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+5087T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174360 | ||||||
| chr6:131174432
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.589+5159A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174432 | ||||||
| chr6:131174457
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.589+5184C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174457 | ||||||
| chr6:131174466
|
G | A | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+5193G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174466 | ||||||
| chr6:131174469
|
G | T | 1 | a0001c0001t0004g0209 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.589+5196G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174469 | ||||||
| chr6:131174532
|
A | G | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+5259A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174532 | ||||||
| chr6:131174556
|
A | G | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+5283A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174556 | ||||||
| chr6:131174587
|
C | T | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5314C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174587 | ||||||
| chr6:131174713
|
C | T | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5440C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174713 | ||||||
| chr6:131174909
|
GAACCCTG others(24): Show |
G | 25 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0164others(22): Show | 25 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.589+5637_589+5667d others(33): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174909 | ||||||
| chr6:131174913
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0003g0073 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.589+5640C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174913 | ||||||
| chr6:131174979
|
AT | A | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5708delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131174979 | |||||
| chr6:131175109
|
C | T | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+5836C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175109 | ||||||
| chr6:131175220
|
T | C | 12 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+5947T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175220 | ||||||
| chr6:131175506
|
G | C | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589+6233G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175506 | ||||||
| chr6:131175511
|
G | T | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.589+6238G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175511 | ||||||
| chr6:131175579
|
A | G | 226 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(223): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.589+6306A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175579 | ||||||
| chr6:131175792
|
T | C | 2 | a0001c0001t0003g0142a0001c0001t0003g0150 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.589+6519T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175792 | ||||||
| chr6:131175912
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.589+6639G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175912 | ||||||
| chr6:131175936
|
G | T | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+6663G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175936 | ||||||
| chr6:131175941
|
T | C | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.589+6668T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175941 | ||||||
| chr6:131175961
|
T | C | 4 | a0002c0002t0001g0157a0006c0006t0014g0003a0006c0006t0016g0005others(1): Show | 4 | HG01123.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+6688T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175961 | ||||||
| chr6:131176079
|
A | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+6806A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176079 | ||||||
| chr6:131176285
|
G | GT | 8 | a0001c0001t0001g0161a0001c0001t0002g0271a0001c0001t0004g0033others(5): Show | 8 | HG03098.hp2 NA18955.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.589+7024dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131176285 | |||||
| chr6:131176285
|
GT | G | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+7024delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131176285 | |||||
| chr6:131176717
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.589+7444C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176717 | ||||||
| chr6:131176718
|
G | A | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+7445G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176718 | ||||||
| chr6:131176817
|
C | A | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+7544C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176817 | ||||||
| chr6:131176857
|
C | A | 2 | a0001c0001t0004g0208a0001c0001t0006g0296 | 2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.589+7584C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176857 | ||||||
| chr6:131176889
|
C | G | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+7616C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176889 | ||||||
| chr6:131177088
|
T | G | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+7815T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177088 | ||||||
| chr6:131177224
|
G | T | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+7951G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177224 | ||||||
| chr6:131177400
|
C | G | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+8127C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177400 | ||||||
| chr6:131177460
|
T | C | 1 | a0002c0002t0003g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589+8187T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177460 | ||||||
| chr6:131177463
|
G | A | 200 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.589+8190G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177463 | ||||||
| chr6:131177469
|
G | A | 51 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(48): Show | 51 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.589+8196G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177469 | ||||||
| chr6:131177663
|
G | A | 3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+8390G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177663 | ||||||
| chr6:131177758
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0153others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+8485C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177758 | ||||||
| chr6:131177823
|
C | T | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+8550C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177823 | ||||||
| chr6:131177850
|
ACCTCTTC others(3): Show |
A | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+8581_589+8590d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131177850 | |||||
| chr6:131178055
|
G | T | 38 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(35): Show | 38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+8782G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178055 | ||||||
| chr6:131178226
|
C | T | 8 | a0001c0001t0005g0156a0001c0001t0007g0282a0001c0001t0009g0221others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+8953C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178226 | ||||||
| chr6:131178237
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0105 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.589+8964T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178237 | ||||||
| chr6:131178302
|
G | A | 225 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(222): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.589+9029G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178302 | ||||||
| chr6:131178306
|
T | C | 1 | a0002c0002t0001g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589+9033T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178306 | ||||||
| chr6:131178379
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.589+9106G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178379 | ||||||
| chr6:131178499
|
A | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9226A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178499 | ||||||
| chr6:131178658
|
A | G | 1 | a0001c0001t0013g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.589+9385A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178658 | ||||||
| chr6:131178763
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9490C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178763 | ||||||
| chr6:131178812
|
G | A | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+9539G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178812 | ||||||
| chr6:131178876
|
A | G | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+9603A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178876 | ||||||
| chr6:131178973
|
A | G | 2 | a0001c0001t0006g0002a0008c0008t0006g0002 | 2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.589+9700A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178973 | ||||||
| chr6:131178990
|
G | T | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+9717G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178990 | ||||||
| chr6:131179041
|
C | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9768C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179041 | ||||||
| chr6:131179166
|
C | T | 131 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.589+9893C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179166 | ||||||
| chr6:131179168
|
GT | G | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(152): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.589+9905delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179168 | |||||
| chr6:131179187
|
G | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9914G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179187 | ||||||
| chr6:131179215
|
C | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+9942C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179215 | ||||||
| chr6:131179258
|
C | T | 43 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.589+9985C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179258 | ||||||
| chr6:131179463
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG01496.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.589+10190C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179463 | ||||||
| chr6:131179529
|
C | T | 1 | a0001c0001t0007g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.589+10256C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179529 | ||||||
| chr6:131179597
|
C | T | 4 | a0001c0001t0007g0277a0002c0002t0015g0008a0002c0002t0015g0009others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+10324C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179597 | ||||||
| chr6:131179602
|
AG | A | 38 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0211others(35): Show | 38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+10331delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179602 | |||||
| chr6:131179868
|
CAAAT | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0164others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.589+10622_589+1062 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179868 | |||||
| chr6:131179895
|
A | T | 190 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(187): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.589+10622A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179895 | ||||||
| chr6:131179896
|
T | A | 191 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(188): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.589+10623T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179896 | ||||||
| chr6:131179896
|
T | TAATA | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+10637_589+1064 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179896 | |||||
| chr6:131179899
|
T | A | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+10626T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179899 | ||||||
| chr6:131179900
|
A | T | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+10627A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179900 | ||||||
| chr6:131180025
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.589+10752G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180025 | ||||||
| chr6:131180072
|
C | T | 2 | a0006c0006t0016g0005a0006c0006t0035g0217 | 2 | HG01123.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.589+10799C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180072 | ||||||
| chr6:131180231
|
T | G | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.589+10958T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180231 | ||||||
| chr6:131180250
|
C | T | 2 | a0001c0001t0005g0224a0001c0001t0007g0281 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.589+10977C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180250 | ||||||
| chr6:131180463
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.589+11190C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180463 | ||||||
| chr6:131180493
|
C | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+11220C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180493 | ||||||
| chr6:131180664
|
C | T | 1 | a0009c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.589+11391C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180664 | ||||||
| chr6:131180694
|
A | G | 42 | a0001c0001t0001g0215a0001c0001t0002g0272a0001c0001t0004g0026others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+11421A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180694 | ||||||
| chr6:131180750
|
A | G | 20 | a0001c0001t0005g0074a0001c0001t0005g0156a0001c0001t0007g0243others(17): Show | 20 | HG01123.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.589+11477A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180750 | ||||||
| chr6:131180812
|
ACTTT | A | 22 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.589+11544_589+1154 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180812 | |||||
| chr6:131180832
|
TTG | T | 18 | a0001c0001t0005g0089a0002c0002t0001g0063a0002c0002t0001g0090others(15): Show | 18 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.589+11561_589+1156 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180832 | |||||
| chr6:131180834
|
G | T | 2 | a0002c0002t0017g0007a0002c0002t0036g0222 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.589+11561G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180834 | ||||||
| chr6:131180834
|
GT | G | 182 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(179): Show | 183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.589+11575delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180834 | |||||
| chr6:131180847
|
TTA | T | 30 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(27): Show | 30 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.589+11575_589+1157 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180847 | ||||||
| chr6:131180848
|
TA | T | 4 | a0001c0001t0021g0223a0001c0001t0022g0085a0001c0001t0022g0095others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+11577delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180848 | |||||
| chr6:131180849
|
A | T | 21 | a0001c0001t0005g0089a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.589+11576A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180849 | ||||||
| chr6:131180866
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0010g0086a0006c0006t0014g0004 | 3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.589+11593A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180866 | ||||||
| chr6:131180945
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.589+11672G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180945 | ||||||
| chr6:131181048
|
G | GC | 127 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.589+11777dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131181048 | |||||
| chr6:131181081
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0010g0086a0001c0001t0034g0219others(1): Show | 4 | HG02280.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+11808G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181081 | ||||||
| chr6:131181190
|
C | A | 6 | a0001c0001t0002g0232a0001c0001t0002g0279a0001c0001t0002g0298others(3): Show | 6 | HG00099.hp2 HG01978.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+11917C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181190 | ||||||
| chr6:131181199
|
A | G | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.589+11926A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181199 | ||||||
| chr6:131181388
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0002g0261 | 2 | NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.589+12115C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181388 | ||||||
| chr6:131181395
|
A | T | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.589+12122A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181395 | ||||||
| chr6:131181453
|
T | G | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+12180T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181453 | ||||||
| chr6:131181488
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+12215G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181488 | ||||||
| chr6:131181506
|
A | T | 16 | a0001c0001t0001g0091a0001c0001t0007g0286a0001c0001t0009g0141others(13): Show | 16 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.589+12233A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181506 | ||||||
| chr6:131181522
|
G | C | 17 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+12249G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181522 | ||||||
| chr6:131181538
|
T | C | 17 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+12265T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181538 | ||||||
| chr6:131181631
|
T | C | 91 | a0001c0001t0002g0248a0001c0001t0004g0026a0001c0001t0004g0033others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.589+12358T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181631 | ||||||
| chr6:131181728
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+12455C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181728 | ||||||
| chr6:131181759
|
T | C | 52 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.589+12486T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181759 | ||||||
| chr6:131181894
|
C | T | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+12621C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181894 | ||||||
| chr6:131182027
|
GA | G | 4 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0007g0277others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+12755delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182027 | ||||||
| chr6:131182125
|
G | GA | 46 | a0001c0001t0002g0248a0002c0002t0001g0027a0002c0002t0001g0063others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.589+12862dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131182125 | |||||
| chr6:131182160
|
A | G | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+12887A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182160 | ||||||
| chr6:131182243
|
A | G | 1 | a0001c0001t0003g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.589+12970A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182243 | ||||||
| chr6:131182509
|
C | T | 29 | a0001c0001t0002g0300a0001c0001t0005g0074a0001c0001t0005g0075others(26): Show | 29 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.589+13236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182509 | ||||||
| chr6:131182669
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+13396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182669 | ||||||
| chr6:131182758
|
C | A | 1 | a0001c0001t0004g0200 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.589+13485C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182758 | ||||||
| chr6:131182816
|
CT | C | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+13552delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131182816 | |||||
| chr6:131182817
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.589+13544T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182817 | ||||||
| chr6:131183147
|
A | G | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.589+13874A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183147 | ||||||
| chr6:131183163
|
CT | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0002g0280others(1): Show | 4 | NA18981.hp2 NA19006.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+13892delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131183163 | |||||
| chr6:131183235
|
A | G | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.589+13962A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183235 | ||||||
| chr6:131183261
|
T | C | 23 | a0001c0001t0002g0248a0001c0001t0034g0219a0002c0002t0001g0027others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.589+13988T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183261 | ||||||
| chr6:131183360
|
T | C | 51 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.589+14087T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183360 | ||||||
| chr6:131183436
|
G | A | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+14163G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183436 | ||||||
| chr6:131183711
|
T | C | 60 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.589+14438T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183711 | ||||||
| chr6:131184003
|
A | C | 1 | a0001c0001t0004g0026 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.589+14730A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184003 | ||||||
| chr6:131184091
|
G | T | 16 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(13): Show | 16 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.589+14818G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184091 | ||||||
| chr6:131184185
|
C | T | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589+14912C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184185 | ||||||
| chr6:131184293
|
T | G | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.589+15020T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184293 | ||||||
| chr6:131184310
|
A | AG | 55 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.589+15043dupG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131184310 | |||||
| chr6:131184313
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+15040G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184313 | ||||||
| chr6:131184315
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589+15042G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184315 | ||||||
| chr6:131184391
|
C | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.590-15070C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184391 | ||||||
| chr6:131184501
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0123 | 2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.590-14960G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184501 | ||||||
| chr6:131184605
|
A | G | 134 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.590-14856A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184605 | ||||||
| chr6:131184779
|
G | A | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.590-14682G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184779 | ||||||
| chr6:131184844
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.590-14617A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184844 | ||||||
| chr6:131184920
|
A | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.590-14541A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184920 | ||||||
| chr6:131185025
|
C | T | 50 | a0001c0001t0002g0248a0001c0001t0034g0219a0002c0002t0001g0027others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.590-14436C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185025 | ||||||
| chr6:131185157
|
A | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-14304A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185157 | ||||||
| chr6:131185533
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.590-13928A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185533 | ||||||
| chr6:131185738
|
C | G | 3 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0024g0160 | 3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.590-13723C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185738 | ||||||
| chr6:131185784
|
A | G | 50 | a0001c0001t0002g0248a0001c0001t0034g0219a0002c0002t0001g0027others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.590-13677A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185784 | ||||||
| chr6:131185814
|
A | C | 55 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.590-13647A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185814 | ||||||
| chr6:131186131
|
G | A | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-13330G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186131 | ||||||
| chr6:131186370
|
G | A | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-13091G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186370 | ||||||
| chr6:131186429
|
A | AT | 6 | a0002c0002t0037g0162a0005c0005t0005g0097a0005c0005t0005g0098others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-13022dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131186429 | |||||
| chr6:131186429
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-13032A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186429 | ||||||
| chr6:131186481
|
C | G | 22 | a0001c0001t0002g0248a0002c0002t0001g0027a0002c0002t0001g0067others(19): Show | 22 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.590-12980C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186481 | ||||||
| chr6:131186558
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.590-12903T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186558 | ||||||
| chr6:131186626
|
A | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-12835A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186626 | ||||||
| chr6:131186804
|
GA | G | 20 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-12655delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131186804 | |||||
| chr6:131187062
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.590-12399A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187062 | ||||||
| chr6:131187142
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.590-12319T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187142 | ||||||
| chr6:131187153
|
A | G | 3 | a0004c0004t0001g0001a0004c0004t0001g0216a0004c0004t0003g0167 | 4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-12308A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187153 | ||||||
| chr6:131187234
|
T | A | 245 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.590-12227T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187234 | ||||||
| chr6:131187255
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.590-12206A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187255 | ||||||
| chr6:131187304
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0010g0086a0006c0006t0014g0004 | 3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.590-12157A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187304 | ||||||
| chr6:131187749
|
A | G | 4 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-11712A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187749 | ||||||
| chr6:131187756
|
A | G | 20 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-11705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187756 | ||||||
| chr6:131187956
|
A | G | 55 | a0001c0001t0002g0248a0001c0001t0005g0074a0001c0001t0005g0075others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.590-11505A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187956 | ||||||
| chr6:131188128
|
A | G | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-11333A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188128 | ||||||
| chr6:131188166
|
A | G | 1 | a0006c0006t0014g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.590-11295A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188166 | ||||||
| chr6:131188237
|
C | CAT | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-11222_590-1122 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188237 | |||||
| chr6:131188494
|
TACTC | T | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-10965_590-1096 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188494 | |||||
| chr6:131188529
|
TTTG | T | 3 | a0001c0001t0007g0243a0001c0001t0041g0158a0002c0002t0027g0231 | 3 | HG02258.hp1 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.590-10917_590-1091 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188529 | |||||
| chr6:131188602
|
A | G | 6 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0224others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-10859A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188602 | ||||||
| chr6:131188710
|
T | C | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-10751T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188710 | ||||||
| chr6:131188717
|
C | CT | 52 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.590-10728dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188717 | |||||
| chr6:131188717
|
CT | C | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-10728delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188717 | |||||
| chr6:131189495
|
AAG | A | 133 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.590-9965_590-9964d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189495 | ||||||
| chr6:131189515
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.590-9946A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189515 | ||||||
| chr6:131189647
|
A | G | 1 | a0004c0004t0003g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.590-9814A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189647 | ||||||
| chr6:131189661
|
G | A | 1 | a0007c0011t0004g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.590-9800G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189661 | ||||||
| chr6:131190048
|
T | C | 1 | a0009c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.590-9413T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190048 | ||||||
| chr6:131190063
|
C | T | 92 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.590-9398C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190063 | ||||||
| chr6:131190107
|
T | C | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-9354T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190107 | ||||||
| chr6:131190127
|
C | G | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-9334C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190127 | ||||||
| chr6:131190149
|
A | G | 21 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(18): Show | 21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.590-9312A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190149 | ||||||
| chr6:131190232
|
T | G | 50 | a0001c0001t0034g0219a0002c0002t0001g0027a0002c0002t0001g0063others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.590-9229T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190232 | ||||||
| chr6:131190290
|
C | G | 10 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(7): Show | 10 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-9171C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190290 | ||||||
| chr6:131190365
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-9096G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190365 | ||||||
| chr6:131190413
|
C | T | 51 | a0001c0001t0034g0219a0001c0001t0041g0158a0002c0002t0001g0027others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.590-9048C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190413 | ||||||
| chr6:131190534
|
C | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-8927C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190534 | ||||||
| chr6:131190846
|
T | G | 1 | a0001c0001t0004g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.590-8615T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190846 | ||||||
| chr6:131190994
|
C | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-8467C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190994 | ||||||
| chr6:131191061
|
C | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0152others(5): Show | 8 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-8400C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191061 | ||||||
| chr6:131191066
|
G | A | 3 | a0001c0001t0007g0282a0001c0001t0028g0236a0006c0006t0016g0005 | 3 | HG01123.hp2 HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.590-8395G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191066 | ||||||
| chr6:131191105
|
A | G | 50 | a0001c0001t0034g0219a0002c0002t0001g0027a0002c0002t0001g0063others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.590-8356A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191105 | ||||||
| chr6:131191205
|
A | T | 2 | a0001c0001t0007g0243a0001c0001t0041g0158 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-8256A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191205 | ||||||
| chr6:131191233
|
A | G | 1 | a0003c0003t0008g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.590-8228A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191233 | ||||||
| chr6:131191618
|
A | C | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-7843A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191618 | ||||||
| chr6:131191749
|
C | T | 302 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.590-7712C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191749 | ||||||
| chr6:131191839
|
C | T | 1 | a0001c0001t0010g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.590-7622C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191839 | ||||||
| chr6:131191845
|
G | GT | 31 | a0001c0001t0002g0298a0001c0001t0003g0150a0002c0002t0001g0063others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.590-7599dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131191845 | |||||
| chr6:131191936
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.590-7525G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191936 | ||||||
| chr6:131192265
|
A | G | 2 | a0002c0002t0001g0120a0002c0002t0002g0288 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.590-7196A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192265 | ||||||
| chr6:131192342
|
G | A | 2 | a0001c0001t0023g0174a0001c0001t0023g0175 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.590-7119G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192342 | ||||||
| chr6:131192427
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-7034A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192427 | ||||||
| chr6:131192521
|
T | C | 297 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.590-6940T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192521 | ||||||
| chr6:131192545
|
A | G | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-6916A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192545 | ||||||
| chr6:131193194
|
A | G | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.590-6267A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193194 | ||||||
| chr6:131193218
|
T | C | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-6243T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193218 | ||||||
| chr6:131193306
|
T | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-6155T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193306 | ||||||
| chr6:131193328
|
A | G | 54 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(51): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.590-6133A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193328 | ||||||
| chr6:131193432
|
G | T | 23 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.590-6029G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193432 | ||||||
| chr6:131193615
|
G | A | 2 | a0001c0001t0005g0156a0001c0001t0007g0251 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.590-5846G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193615 | ||||||
| chr6:131193722
|
AT | A | 3 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0024g0160 | 3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.590-5738delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193722 | ||||||
| chr6:131193754
|
G | A | 134 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.590-5707G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193754 | ||||||
| chr6:131194092
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.590-5369C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194092 | ||||||
| chr6:131194106
|
G | A | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-5355G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194106 | ||||||
| chr6:131194149
|
C | CT | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-5304dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131194149 | |||||
| chr6:131194283
|
T | C | 49 | a0002c0002t0001g0027a0002c0002t0001g0063a0002c0002t0001g0067others(46): Show | 49 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.590-5178T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194283 | ||||||
| chr6:131194355
|
T | C | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-5106T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194355 | ||||||
| chr6:131194364
|
T | C | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-5097T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194364 | ||||||
| chr6:131194404
|
T | A | 4 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(1): Show | 4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-5057T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194404 | ||||||
| chr6:131194406
|
A | T | 4 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(1): Show | 4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-5055A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194406 | ||||||
| chr6:131194535
|
A | G | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-4926A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194535 | ||||||
| chr6:131194610
|
A | G | 109 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.590-4851A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194610 | ||||||
| chr6:131194614
|
C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-4847C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194614 | ||||||
| chr6:131194827
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0002g0288 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.590-4634G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194827 | ||||||
| chr6:131194901
|
T | A | 20 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-4560T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194901 | ||||||
| chr6:131195109
|
C | T | 254 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.590-4352C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195109 | ||||||
| chr6:131195300
|
C | T | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-4161C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195300 | ||||||
| chr6:131195469
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.590-3992A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195469 | ||||||
| chr6:131195521
|
C | G | 1 | a0001c0001t0005g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.590-3940C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195521 | ||||||
| chr6:131195895
|
C | T | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-3566C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195895 | ||||||
| chr6:131195954
|
A | G | 4 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-3507A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195954 | ||||||
| chr6:131196267
|
C | CT | 136 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.590-3178dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131196267 | |||||
| chr6:131196292
|
G | A | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-3169G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196292 | ||||||
| chr6:131196329
|
A | G | 1 | a0001c0001t0023g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.590-3132A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196329 | ||||||
| chr6:131196389
|
C | T | 2 | a0002c0002t0001g0135a0002c0002t0001g0136 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.590-3072C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196389 | ||||||
| chr6:131196405
|
A | G | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-3056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196405 | ||||||
| chr6:131196452
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-3009C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196452 | ||||||
| chr6:131196554
|
G | A | 21 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(18): Show | 21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.590-2907G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196554 | ||||||
| chr6:131196626
|
A | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2835A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196626 | ||||||
| chr6:131196678
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.590-2783A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196678 | ||||||
| chr6:131196687
|
T | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2774T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196687 | ||||||
| chr6:131196690
|
A | C | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.590-2771A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196690 | ||||||
| chr6:131196695
|
A | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-2766A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196695 | ||||||
| chr6:131196740
|
T | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2721T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196740 | ||||||
| chr6:131196761
|
A | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-2700A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196761 | ||||||
| chr6:131196955
|
T | C | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-2506T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196955 | ||||||
| chr6:131197097
|
T | C | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-2364T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197097 | ||||||
| chr6:131197140
|
C | G | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.590-2321C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197140 | ||||||
| chr6:131197459
|
A | G | 1 | a0001c0001t0006g0296 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.590-2002A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197459 | ||||||
| chr6:131197583
|
A | T | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.590-1878A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197583 | ||||||
| chr6:131197732
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.590-1729A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197732 | ||||||
| chr6:131197754
|
T | C | 136 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.590-1707T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197754 | ||||||
| chr6:131198090
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.590-1371C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198090 | ||||||
| chr6:131198096
|
G | A | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-1365G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198096 | ||||||
| chr6:131198199
|
A | G | 8 | a0001c0001t0001g0045a0001c0001t0003g0040a0001c0001t0003g0041others(5): Show | 8 | NA18943.hp1 NA18951.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-1262A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198199 | ||||||
| chr6:131198229
|
T | C | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.590-1232T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198229 | ||||||
| chr6:131198523
|
A | G | 2 | a0001c0001t0007g0243a0001c0001t0041g0158 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-938A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198523 | ||||||
| chr6:131198555
|
T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-906T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198555 | ||||||
| chr6:131198560
|
A | G | 11 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-901A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198560 | ||||||
| chr6:131198592
|
G | A | 1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.590-869G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198592 | ||||||
| chr6:131198851
|
C | A | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.590-610C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198851 | ||||||
| chr6:131198895
|
TCTTA | T | 5 | a0001c0001t0005g0140a0001c0001t0009g0184a0001c0001t0021g0223others(2): Show | 5 | HG02922.hp1 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-562_590-559del others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131198895 | |||||
| chr6:131198980
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.590-481A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198980 | ||||||
| chr6:131198984
|
G | C | 254 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.590-477G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198984 | ||||||
| chr6:131199038
|
G | A | 2 | a0001c0001t0007g0243a0001c0001t0041g0158 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-423G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199038 | ||||||
| chr6:131199149
|
A | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-312A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199149 | ||||||
| chr6:131199298
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-163G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199298 | ||||||
| chr6:131199367
|
A | G | 20 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-94A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199367 | ||||||
| chr6:131199597
|
G | T | 1 | a0001c0001t0002g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.702+24G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199597 | ||||||
| chr6:131199754
|
T | C | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+181T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199754 | ||||||
| chr6:131199827
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.702+254C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199827 | ||||||
| chr6:131199854
|
C | A | 21 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(18): Show | 21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+281C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199854 | ||||||
| chr6:131199947
|
C | G | 1 | a0001c0001t0002g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.702+374C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199947 | ||||||
| chr6:131200234
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+661G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200234 | ||||||
| chr6:131200414
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+841C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200414 | ||||||
| chr6:131200564
|
G | A | 20 | a0002c0002t0001g0063a0002c0002t0001g0090a0002c0002t0001g0096others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+991G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200564 | ||||||
| chr6:131200688
|
T | C | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+1115T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200688 | ||||||
| chr6:131200690
|
A | G | 97 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.702+1117A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200690 | ||||||
| chr6:131200807
|
C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+1234C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200807 | ||||||
| chr6:131200821
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+1248A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200821 | ||||||
| chr6:131200853
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.702+1280G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200853 | ||||||
| chr6:131200881
|
T | C | 1 | a0001c0001t0002g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.702+1308T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200881 | ||||||
| chr6:131200969
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.702+1396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200969 | ||||||
| chr6:131201072
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+1499T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201072 | ||||||
| chr6:131201269
|
A | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.702+1696A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201269 | ||||||
| chr6:131201342
|
C | T | 21 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(18): Show | 21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1769C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201342 | ||||||
| chr6:131201352
|
A | G | 12 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0156others(9): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+1779A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201352 | ||||||
| chr6:131201372
|
A | G | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1799A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201372 | ||||||
| chr6:131201434
|
A | G | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1861A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201434 | ||||||
| chr6:131201472
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.702+1899C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201472 | ||||||
| chr6:131201659
|
T | C | 8 | a0001c0001t0002g0300a0001c0001t0005g0092a0001c0001t0005g0224others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+2086T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201659 | ||||||
| chr6:131201766
|
T | A | 1 | a0009c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+2193T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201766 | ||||||
| chr6:131201786
|
G | A | 3 | a0002c0002t0001g0181a0002c0002t0001g0182a0002c0002t0002g0235 | 3 | HG00140.hp2 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.702+2213G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201786 | ||||||
| chr6:131201835
|
T | C | 10 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(7): Show | 10 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+2262T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201835 | ||||||
| chr6:131201861
|
A | G | 136 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.702+2288A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201861 | ||||||
| chr6:131201932
|
T | C | 98 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.702+2359T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201932 | ||||||
| chr6:131201933
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+2360A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201933 | ||||||
| chr6:131202024
|
T | G | 1 | a0002c0002t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.702+2451T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202024 | ||||||
| chr6:131202046
|
C | A | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2473C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202046 | ||||||
| chr6:131202088
|
G | A | 92 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.702+2515G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202088 | ||||||
| chr6:131202303
|
G | A | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.702+2730G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202303 | ||||||
| chr6:131202394
|
A | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.702+2821A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202394 | ||||||
| chr6:131202526
|
T | C | 255 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.702+2953T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202526 | ||||||
| chr6:131202568
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.702+2995C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202568 | ||||||
| chr6:131202595
|
C | T | 124 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.702+3022C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202595 | ||||||
| chr6:131202689
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.702+3116G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202689 | ||||||
| chr6:131202733
|
C | T | 1 | a0001c0001t0009g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.702+3160C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202733 | ||||||
| chr6:131202762
|
TAATAA | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | NA18964.hp1 NA18982.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.702+3206_702+3210d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131202762 | |||||
| chr6:131203037
|
G | A | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.702+3464G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203037 | ||||||
| chr6:131203198
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+3625C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203198 | ||||||
| chr6:131203218
|
A | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.702+3645A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203218 | ||||||
| chr6:131203374
|
C | T | 10 | a0001c0001t0010g0081a0001c0001t0023g0174a0001c0001t0023g0175others(7): Show | 10 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3801C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203374 | ||||||
| chr6:131203478
|
G | A | 32 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(29): Show | 32 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.702+3905G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203478 | ||||||
| chr6:131203854
|
C | T | 12 | a0001c0001t0004g0033a0001c0001t0004g0035a0001c0001t0004g0036others(9): Show | 12 | NA18612.hp1 NA18942.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+4281C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203854 | ||||||
| chr6:131203859
|
A | G | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.702+4286A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203859 | ||||||
| chr6:131204108
|
C | T | 15 | a0001c0001t0001g0091a0001c0001t0007g0286a0001c0001t0010g0081others(12): Show | 15 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4535C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204108 | ||||||
| chr6:131204402
|
A | C | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.702+4829A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204402 | ||||||
| chr6:131204415
|
C | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+4842C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204415 | ||||||
| chr6:131204544
|
A | G | 55 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+4971A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204544 | ||||||
| chr6:131204749
|
G | A | 55 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+5176G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204749 | ||||||
| chr6:131204754
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.702+5181C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204754 | ||||||
| chr6:131204843
|
G | A | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.702+5270G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204843 | ||||||
| chr6:131205046
|
TA | T | 9 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(6): Show | 9 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.702+5478delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131205046 | |||||
| chr6:131205365
|
A | G | 120 | a0001c0001t0002g0300a0001c0001t0004g0026a0001c0001t0004g0033others(117): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.702+5792A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205365 | ||||||
| chr6:131205383
|
C | T | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.702+5810C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205383 | ||||||
| chr6:131205448
|
C | T | 2 | a0001c0001t0007g0282a0001c0001t0028g0236 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+5875C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205448 | ||||||
| chr6:131205449
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+5876C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205449 | ||||||
| chr6:131206197
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.702+6624A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206197 | ||||||
| chr6:131206332
|
A | G | 9 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+6759A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206332 | ||||||
| chr6:131206565
|
A | G | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.702+6992A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206565 | ||||||
| chr6:131206607
|
T | A | 2 | a0002c0002t0001g0177a0002c0002t0002g0265 | 2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.702+7034T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206607 | ||||||
| chr6:131206647
|
G | C | 1 | a0001c0001t0003g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.702+7074G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206647 | ||||||
| chr6:131206775
|
G | A | 187 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(184): Show | 187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.702+7202G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206775 | ||||||
| chr6:131206786
|
C | CATCT | 26 | a0001c0001t0003g0056a0001c0001t0005g0156a0001c0001t0007g0243others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.702+7234_702+7237d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131206786 | |||||
| chr6:131206790
|
T | C | 1 | a0003c0003t0032g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.702+7217T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206790 | ||||||
| chr6:131206809
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.702+7236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206809 | ||||||
| chr6:131207130
|
C | T | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+7557C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207130 | ||||||
| chr6:131207318
|
A | AT | 53 | a0001c0001t0001g0083a0001c0001t0001g0152a0001c0001t0001g0153others(50): Show | 53 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.702+7760dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207318 | |||||
| chr6:131207318
|
AT | A | 21 | a0001c0001t0002g0238a0001c0001t0003g0072a0001c0001t0004g0059others(18): Show | 21 | HG00323.hp2 HG01993.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.702+7760delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207318 | |||||
| chr6:131207421
|
A | G | 1 | a0002c0002t0039g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.702+7848A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207421 | ||||||
| chr6:131207491
|
A | AT | 11 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0179others(8): Show | 11 | HG01123.hp2 HG01943.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+7944dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATATATTT others(9): Show |
1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.702+7919_702+7920i others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0006g0253a0001c0001t0022g0085a0005c0005t0005g0097 | 3 | HG02451.hp2 HG02717.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.702+7935_702+7944d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(4): Show |
20 | a0001c0001t0004g0196a0001c0001t0004g0197a0001c0001t0004g0199others(17): Show | 20 | HG00408.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.702+7934_702+7944d others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(5): Show |
15 | a0001c0001t0004g0059a0001c0001t0004g0168a0001c0001t0004g0169others(12): Show | 15 | HG01993.hp2 HG02257.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+7933_702+7944d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(6): Show |
12 | a0001c0001t0004g0026a0001c0001t0004g0035a0001c0001t0004g0036others(9): Show | 12 | HG00597.hp1 HG01516.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+7932_702+7944d others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(7): Show |
5 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0186others(2): Show | 5 | NA18953.hp1 NA18965.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+7931_702+7944d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(8): Show |
3 | a0001c0001t0004g0178a0001c0001t0004g0191a0002c0002t0002g0265 | 3 | HG03017.hp2 NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.702+7930_702+7944d others(17): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0012g0057a0002c0002t0001g0133a0002c0002t0001g0157others(1): Show | 4 | HG01978.hp2 HG02074.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+7929_702+7944d others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(10): Show |
14 | a0001c0001t0001g0083a0001c0001t0001g0153a0002c0002t0001g0096others(11): Show | 14 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+7928_702+7944d others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(11): Show |
17 | a0002c0002t0001g0027a0002c0002t0001g0063a0002c0002t0001g0067others(14): Show | 17 | HG01109.hp2 HG01123.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.702+7927_702+7944d others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(12): Show |
2 | a0002c0002t0001g0159a0002c0002t0002g0245 | 2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.702+7926_702+7944d others(21): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+7925_702+7944d others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(14): Show |
1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.702+7924_702+7944d others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(15): Show |
1 | a0002c0002t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.702+7923_702+7944d others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
A | ATTTTTTT others(16): Show |
1 | a0002c0002t0039g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.702+7922_702+7944d others(25): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
AT | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0115others(13): Show | 16 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.702+7944delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
ATT | A | 6 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+7943_702+7944d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207491
|
ATTTT | A | 6 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(3): Show | 6 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+7941_702+7944d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | |||||
| chr6:131207493
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+7920T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207493 | ||||||
| chr6:131207517
|
T | TTTTTTTT others(4): Show |
1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.702+7944_702+7945i others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | ||||||
| chr6:131207517
|
T | TTTTTTTT others(5): Show |
3 | a0002c0002t0017g0007a0002c0002t0017g0010a0002c0002t0036g0222 | 3 | HG02257.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.702+7944_702+7945i others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | ||||||
| chr6:131207517
|
T | TTTTTTTT others(14): Show |
1 | a0002c0002t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+7944_702+7945i others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | ||||||
| chr6:131207728
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702+8155G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207728 | ||||||
| chr6:131207802
|
C | T | 3 | a0004c0004t0001g0001a0004c0004t0001g0216a0004c0004t0003g0167 | 4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+8229C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207802 | ||||||
| chr6:131207962
|
C | T | 12 | a0001c0001t0005g0094a0001c0001t0007g0286a0001c0001t0010g0081others(9): Show | 12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+8389C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207962 | ||||||
| chr6:131207963
|
G | A | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+8390G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207963 | ||||||
| chr6:131208500
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0002g0267a0001c0001t0002g0275 | 3 | HG00544.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.702+8927T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131208500 | ||||||
| chr6:131209010
|
C | T | 5 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+9437C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209010 | ||||||
| chr6:131209150
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.702+9577A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209150 | ||||||
| chr6:131209173
|
AT | A | 22 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(19): Show | 22 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+9611delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131209173 | |||||
| chr6:131209180
|
T | A | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+9607T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209180 | ||||||
| chr6:131209241
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702+9668A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209241 | ||||||
| chr6:131209257
|
T | G | 1 | a0009c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+9684T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209257 | ||||||
| chr6:131209293
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+9720C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209293 | ||||||
| chr6:131209388
|
C | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+9815C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209388 | ||||||
| chr6:131209441
|
G | A | 24 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.702+9868G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209441 | ||||||
| chr6:131209733
|
G | GT | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-9923dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131209733 | |||||
| chr6:131209740
|
G | C | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.703-9921G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209740 | ||||||
| chr6:131209811
|
A | G | 2 | a0006c0006t0014g0003a0006c0006t0014g0004 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.703-9850A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209811 | ||||||
| chr6:131209844
|
A | T | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-9817A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209844 | ||||||
| chr6:131209876
|
C | T | 62 | a0001c0001t0001g0083a0001c0001t0005g0074a0001c0001t0005g0075others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-9785C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209876 | ||||||
| chr6:131210046
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0003g0044 | 3 | NA19006.hp2 NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.703-9615A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210046 | ||||||
| chr6:131210097
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703-9564T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210097 | ||||||
| chr6:131210166
|
A | T | 62 | a0001c0001t0001g0083a0001c0001t0005g0074a0001c0001t0005g0075others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-9495A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210166 | ||||||
| chr6:131210172
|
C | T | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703-9489C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210172 | ||||||
| chr6:131210330
|
G | A | 2 | a0002c0002t0001g0177a0002c0002t0002g0265 | 2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.703-9331G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210330 | ||||||
| chr6:131210606
|
C | T | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-9055C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210606 | ||||||
| chr6:131210710
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.703-8951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210710 | ||||||
| chr6:131210928
|
T | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.703-8733T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210928 | ||||||
| chr6:131211505
|
C | T | 3 | a0002c0002t0001g0090a0002c0002t0003g0132a0002c0002t0003g0134 | 3 | HG01255.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.703-8156C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211505 | ||||||
| chr6:131211523
|
T | C | 62 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-8138T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211523 | ||||||
| chr6:131211547
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.703-8114C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211547 | ||||||
| chr6:131211601
|
T | TA | 15 | a0001c0001t0001g0045a0001c0001t0001g0213a0001c0001t0003g0040others(12): Show | 15 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.703-8047dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211601 | |||||
| chr6:131211646
|
A | G | 2 | a0001c0001t0005g0094a0001c0001t0007g0286 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.703-8015A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211646 | ||||||
| chr6:131211729
|
C | T | 3 | a0001c0001t0003g0046a0001c0001t0003g0047a0001c0001t0003g0072 | 3 | NA18980.hp2 NA19058.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.703-7932C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211729 | ||||||
| chr6:131211772
|
C | CA | 114 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0083others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.703-7868dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | |||||
| chr6:131211772
|
C | CAA | 11 | a0001c0001t0004g0168a0001c0001t0004g0196a0001c0001t0004g0208others(8): Show | 11 | HG00408.hp2 HG00597.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.703-7869_703-7868d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | |||||
| chr6:131211772
|
C | CAAAAA | 6 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-7872_703-7868d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | |||||
| chr6:131211772
|
CAAAAAAA | C | 44 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-7874_703-7868d others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | |||||
| chr6:131211819
|
A | G | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.703-7842A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211819 | ||||||
| chr6:131211853
|
G | A | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.703-7808G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211853 | ||||||
| chr6:131212156
|
C | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.703-7505C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212156 | ||||||
| chr6:131212173
|
T | G | 16 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(13): Show | 16 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.703-7488T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212173 | ||||||
| chr6:131212216
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.703-7445T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212216 | ||||||
| chr6:131212248
|
G | T | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-7413G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212248 | ||||||
| chr6:131212257
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.703-7404C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212257 | ||||||
| chr6:131212357
|
T | C | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-7304T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212357 | ||||||
| chr6:131212454
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.703-7207T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212454 | ||||||
| chr6:131212466
|
T | C | 1 | a0002c0002t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.703-7195T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212466 | ||||||
| chr6:131212521
|
C | T | 2 | a0001c0001t0004g0208a0001c0001t0006g0296 | 2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.703-7140C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212521 | ||||||
| chr6:131212542
|
C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703-7119C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212542 | ||||||
| chr6:131212550
|
T | C | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-7111T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212550 | ||||||
| chr6:131212681
|
A | C | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-6980A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212681 | ||||||
| chr6:131212821
|
T | A | 2 | a0001c0001t0001g0171a0001c0001t0003g0058 | 2 | HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.703-6840T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212821 | ||||||
| chr6:131213163
|
T | G | 1 | a0001c0001t0004g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-6498T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213163 | ||||||
| chr6:131213234
|
T | C | 120 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0001g0225others(117): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.703-6427T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213234 | ||||||
| chr6:131213263
|
T | A | 58 | a0001c0001t0001g0083a0001c0001t0001g0225a0002c0002t0001g0027others(55): Show | 58 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.703-6398T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213263 | ||||||
| chr6:131213321
|
C | T | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-6340C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213321 | ||||||
| chr6:131213569
|
G | A | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-6092G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213569 | ||||||
| chr6:131213902
|
T | C | 200 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.703-5759T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213902 | ||||||
| chr6:131213973
|
G | A | 2 | a0001c0001t0006g0002a0008c0008t0006g0002 | 2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.703-5688G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213973 | ||||||
| chr6:131214118
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-5543G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214118 | ||||||
| chr6:131214201
|
G | C | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.703-5460G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214201 | ||||||
| chr6:131214356
|
C | A | 15 | a0001c0001t0001g0091a0001c0001t0005g0094a0001c0001t0007g0286others(12): Show | 15 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5305C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214356 | ||||||
| chr6:131214477
|
T | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0194others(7): Show | 10 | HG02155.hp1 NA18946.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-5184T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214477 | ||||||
| chr6:131214840
|
G | A | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-4821G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214840 | ||||||
| chr6:131214899
|
C | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-4762C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214899 | ||||||
| chr6:131215012
|
TG | T | 43 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.703-4647delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131215012 | |||||
| chr6:131215111
|
A | AT | 17 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(14): Show | 17 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.703-4541dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131215111 | |||||
| chr6:131215143
|
G | A | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.703-4518G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215143 | ||||||
| chr6:131215353
|
C | A | 3 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0024g0160 | 3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.703-4308C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215353 | ||||||
| chr6:131215935
|
T | C | 24 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.703-3726T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215935 | ||||||
| chr6:131215952
|
A | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-3709A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215952 | ||||||
| chr6:131216086
|
A | G | 10 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-3575A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216086 | ||||||
| chr6:131216468
|
T | C | 3 | a0001c0001t0001g0225a0002c0002t0020g0149a0006c0006t0035g0217 | 3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.703-3193T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216468 | ||||||
| chr6:131216666
|
G | C | 1 | a0001c0001t0003g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.703-2995G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216666 | ||||||
| chr6:131216747
|
C | T | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.703-2914C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216747 | ||||||
| chr6:131216828
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.703-2833T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216828 | ||||||
| chr6:131217045
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.703-2616A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217045 | ||||||
| chr6:131217237
|
T | G | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-2424T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217237 | ||||||
| chr6:131217332
|
G | A | 168 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.703-2329G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217332 | ||||||
| chr6:131217448
|
A | G | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2213A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217448 | ||||||
| chr6:131217474
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0010g0086a0006c0006t0014g0004 | 3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.703-2187A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217474 | ||||||
| chr6:131217520
|
A | G | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2141A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217520 | ||||||
| chr6:131217548
|
C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703-2113C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217548 | ||||||
| chr6:131217614
|
T | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-2047T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217614 | ||||||
| chr6:131217621
|
T | C | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-2040T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217621 | ||||||
| chr6:131217674
|
G | A | 2 | a0001c0001t0023g0174a0001c0001t0023g0175 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.703-1987G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217674 | ||||||
| chr6:131217788
|
C | T | 3 | a0004c0004t0001g0001a0004c0004t0001g0216a0004c0004t0003g0167 | 4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1873C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217788 | ||||||
| chr6:131217812
|
C | A | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-1849C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217812 | ||||||
| chr6:131217979
|
T | C | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-1682T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217979 | ||||||
| chr6:131218057
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.703-1604A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218057 | ||||||
| chr6:131218234
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.703-1427C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218234 | ||||||
| chr6:131218277
|
C | T | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.703-1384C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218277 | ||||||
| chr6:131218453
|
GA | G | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-1203delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131218453 | |||||
| chr6:131218478
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-1183G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218478 | ||||||
| chr6:131218520
|
A | T | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.703-1141A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218520 | ||||||
| chr6:131218561
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0016g0006a0001c0001t0033g0100 | 3 | HG02818.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.703-1100T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218561 | ||||||
| chr6:131218578
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-1083A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218578 | ||||||
| chr6:131218675
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.703-986C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218675 | ||||||
| chr6:131218711
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703-950T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218711 | ||||||
| chr6:131218834
|
G | A | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-827G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218834 | ||||||
| chr6:131218909
|
T | C | 4 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-752T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218909 | ||||||
| chr6:131218950
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.703-711A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218950 | ||||||
| chr6:131219289
|
C | CA | 6 | a0001c0001t0001g0018a0001c0001t0001g0104a0001c0001t0002g0237others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-353dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131219289 | |||||
| chr6:131219289
|
CA | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(54): Show |
intron_variant | MODIFIER | c.703-353delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131219289 | |||||
| chr6:131219586
|
A | T | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.703-75A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131219586 | ||||||
| chr6:131219826
|
A | G | 10 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+18A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131219826 | ||||||
| chr6:131219916
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.850+108A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131219916 | ||||||
| chr6:131220118
|
T | C | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+310T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220118 | ||||||
| chr6:131220172
|
T | C | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.850+364T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220172 | ||||||
| chr6:131220269
|
T | C | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850+461T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220269 | ||||||
| chr6:131220298
|
G | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+490G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220298 | ||||||
| chr6:131220473
|
A | T | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+665A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220473 | ||||||
| chr6:131220498
|
T | A | 3 | a0001c0001t0001g0226a0001c0001t0016g0006a0001c0001t0033g0100 | 3 | HG02818.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.850+690T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220498 | ||||||
| chr6:131221098
|
A | C | 62 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.850+1290A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221098 | ||||||
| chr6:131221361
|
A | T | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+1553A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221361 | ||||||
| chr6:131221397
|
A | G | 6 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+1589A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221397 | ||||||
| chr6:131221400
|
G | A | 2 | a0001c0001t0007g0243a0001c0001t0009g0221 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+1592G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221400 | ||||||
| chr6:131221448
|
C | A | 2 | a0005c0005t0011g0139a0005c0005t0011g0165 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.850+1640C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221448 | ||||||
| chr6:131221503
|
T | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.850+1695T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221503 | ||||||
| chr6:131221799
|
C | T | 2 | a0002c0002t0003g0048a0002c0002t0003g0050 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.850+1991C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221799 | ||||||
| chr6:131221942
|
A | G | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+2134A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221942 | ||||||
| chr6:131222297
|
G | A | 1 | a0009c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850+2489G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222297 | ||||||
| chr6:131222321
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.850+2513C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222321 | ||||||
| chr6:131222383
|
C | T | 5 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2575C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222383 | ||||||
| chr6:131222435
|
G | A | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+2627G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222435 | ||||||
| chr6:131222543
|
A | T | 5 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2735A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222543 | ||||||
| chr6:131222555
|
A | G | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850+2747A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222555 | ||||||
| chr6:131222624
|
A | G | 1 | a0003c0003t0019g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850+2816A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222624 | ||||||
| chr6:131222926
|
C | A | 2 | a0001c0001t0007g0243a0001c0001t0009g0221 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+3118C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222926 | ||||||
| chr6:131223207
|
A | G | 12 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+3399A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223207 | ||||||
| chr6:131223564
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0151others(2): Show | 5 | HG01074.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+3756C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223564 | ||||||
| chr6:131223620
|
A | G | 10 | a0001c0001t0010g0081a0001c0001t0023g0174a0001c0001t0023g0175others(7): Show | 10 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.850+3812A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223620 | ||||||
| chr6:131223864
|
A | G | 1 | a0001c0001t0020g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850+4056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223864 | ||||||
| chr6:131224118
|
C | T | 2 | a0006c0006t0014g0003a0006c0006t0014g0004 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+4310C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224118 | ||||||
| chr6:131224225
|
T | C | 1 | a0002c0002t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850+4417T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224225 | ||||||
| chr6:131224251
|
A | G | 1 | a0002c0002t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.850+4443A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224251 | ||||||
| chr6:131224414
|
C | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+4606C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224414 | ||||||
| chr6:131224418
|
G | A | 4 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(1): Show | 4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+4610G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224418 | ||||||
| chr6:131224464
|
A | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+4656A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224464 | ||||||
| chr6:131224598
|
A | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+4790A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224598 | ||||||
| chr6:131224708
|
T | A | 15 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(12): Show | 15 | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+4900T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224708 | ||||||
| chr6:131224709
|
GTAAAGTT others(7): Show |
G | 15 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(12): Show | 15 | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+4902_850+4915d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224709 | ||||||
| chr6:131224715
|
T | G | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4907T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224715 | ||||||
| chr6:131224716
|
T | A | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4908T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224716 | ||||||
| chr6:131224718
|
C | T | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4910C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224718 | ||||||
| chr6:131224721
|
G | C | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4913G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224721 | ||||||
| chr6:131224728
|
C | T | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4920C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224728 | ||||||
| chr6:131224729
|
A | T | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4921A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224729 | ||||||
| chr6:131224730
|
C | CT | 36 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0211others(33): Show | 36 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+4951dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | |||||
| chr6:131224730
|
C | T | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4922C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224730 | ||||||
| chr6:131224730
|
CT | C | 96 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 96 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.850+4951delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | |||||
| chr6:131224730
|
CTT | C | 36 | a0001c0001t0001g0083a0001c0001t0001g0172a0001c0001t0002g0289others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+4950_850+4951d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | |||||
| chr6:131224730
|
CTTTTT | C | 6 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(3): Show | 6 | HG02922.hp1 HG03139.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+4947_850+4951d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | |||||
| chr6:131224830
|
A | C | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+5022A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224830 | ||||||
| chr6:131225244
|
G | A | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+5436G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225244 | ||||||
| chr6:131225888
|
A | T | 81 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.850+6080A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225888 | ||||||
| chr6:131225991
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.850+6183A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225991 | ||||||
| chr6:131226119
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+6311G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226119 | ||||||
| chr6:131226201
|
A | G | 81 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.850+6393A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226201 | ||||||
| chr6:131226244
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.850+6436A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226244 | ||||||
| chr6:131226324
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.850+6516A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226324 | ||||||
| chr6:131226352
|
T | C | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+6544T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226352 | ||||||
| chr6:131226438
|
C | T | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+6630C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226438 | ||||||
| chr6:131226440
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.850+6632C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226440 | ||||||
| chr6:131226705
|
T | A | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+6897T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226705 | ||||||
| chr6:131226763
|
TTTTG | T | 6 | a0002c0002t0002g0244a0005c0005t0005g0097a0005c0005t0005g0098others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+6972_850+6975d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131226763 | |||||
| chr6:131226950
|
A | G | 1 | a0001c0001t0025g0066 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.850+7142A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226950 | ||||||
| chr6:131227163
|
G | A | 12 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+7355G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227163 | ||||||
| chr6:131227256
|
T | C | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+7448T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227256 | ||||||
| chr6:131227297
|
A | C | 1 | a0001c0001t0003g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.850+7489A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227297 | ||||||
| chr6:131227389
|
G | C | 2 | a0001c0001t0002g0269a0001c0001t0002g0270 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.850+7581G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227389 | ||||||
| chr6:131227539
|
A | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+7731A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227539 | ||||||
| chr6:131227731
|
A | G | 12 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+7923A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227731 | ||||||
| chr6:131227920
|
T | C | 105 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0004g0026others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.850+8112T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227920 | ||||||
| chr6:131227961
|
T | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+8153T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227961 | ||||||
| chr6:131228027
|
G | C | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+8219G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228027 | ||||||
| chr6:131228048
|
C | T | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+8240C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228048 | ||||||
| chr6:131228095
|
T | C | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.850+8287T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228095 | ||||||
| chr6:131228193
|
G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+8385G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228193 | ||||||
| chr6:131228707
|
C | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+8899C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228707 | ||||||
| chr6:131228729
|
T | G | 12 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+8921T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228729 | ||||||
| chr6:131228735
|
G | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+8927G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228735 | ||||||
| chr6:131229009
|
G | A | 7 | a0002c0002t0001g0090a0002c0002t0001g0096a0002c0002t0002g0244others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+9201G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229009 | ||||||
| chr6:131229057
|
C | T | 5 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+9249C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229057 | ||||||
| chr6:131229063
|
T | TAA | 10 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+9256_850+9257i others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131229063 | |||||
| chr6:131229107
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.850+9299C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229107 | ||||||
| chr6:131229439
|
C | T | 24 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.850+9631C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229439 | ||||||
| chr6:131229551
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+9743G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229551 | ||||||
| chr6:131229586
|
T | A | 6 | a0001c0001t0007g0251a0001c0001t0031g0285a0001c0001t0038g0166others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+9778T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229586 | ||||||
| chr6:131230098
|
C | T | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+10290C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230098 | ||||||
| chr6:131230104
|
G | A | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+10296G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230104 | ||||||
| chr6:131230303
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.850+10495A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230303 | ||||||
| chr6:131230455
|
G | A | 69 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.850+10647G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230455 | ||||||
| chr6:131230502
|
G | T | 12 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+10694G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230502 | ||||||
| chr6:131230635
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+10827G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230635 | ||||||
| chr6:131230950
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.850+11142T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230950 | ||||||
| chr6:131231230
|
T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+11422T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231230 | ||||||
| chr6:131231361
|
G | GT | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+11562dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131231361 | |||||
| chr6:131231617
|
C | T | 1 | a0004c0004t0003g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.850+11809C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231617 | ||||||
| chr6:131231710
|
A | G | 20 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.850+11902A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231710 | ||||||
| chr6:131231731
|
A | G | 10 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+11923A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231731 | ||||||
| chr6:131231760
|
A | G | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+11952A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231760 | ||||||
| chr6:131231831
|
C | T | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.850+12023C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231831 | ||||||
| chr6:131231884
|
G | T | 5 | a0001c0001t0004g0201a0001c0001t0004g0203a0001c0001t0004g0204others(2): Show | 5 | HG01978.hp2 NA18941.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+12076G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231884 | ||||||
| chr6:131231984
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+12176C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231984 | ||||||
| chr6:131232062
|
A | T | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.850+12254A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232062 | ||||||
| chr6:131232066
|
G | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+12258G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232066 | ||||||
| chr6:131232078
|
A | G | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+12270A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232078 | ||||||
| chr6:131232123
|
G | A | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+12315G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232123 | ||||||
| chr6:131232132
|
A | G | 5 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+12324A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232132 | ||||||
| chr6:131232552
|
C | G | 56 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+12744C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232552 | ||||||
| chr6:131232682
|
A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+12874A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232682 | ||||||
| chr6:131232846
|
A | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+13038A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232846 | ||||||
| chr6:131232969
|
T | TAA | 170 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(167): Show | 170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.850+13162_850+1316 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131232969 | |||||
| chr6:131233018
|
A | G | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+13210A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233018 | ||||||
| chr6:131233044
|
C | T | 78 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.850+13236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233044 | ||||||
| chr6:131233142
|
T | TA | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+13341dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131233142 | |||||
| chr6:131233151
|
C | T | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.850+13343C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233151 | ||||||
| chr6:131233295
|
G | C | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+13487G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233295 | ||||||
| chr6:131233327
|
T | G | 1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.850+13519T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233327 | ||||||
| chr6:131233413
|
A | T | 194 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(191): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.850+13605A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233413 | ||||||
| chr6:131233422
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+13614G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233422 | ||||||
| chr6:131233428
|
A | G | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.850+13620A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233428 | ||||||
| chr6:131233604
|
A | T | 1 | a0001c0001t0010g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+13796A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233604 | ||||||
| chr6:131233769
|
A | G | 21 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+13961A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233769 | ||||||
| chr6:131234162
|
A | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+14354A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234162 | ||||||
| chr6:131234251
|
T | C | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+14443T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234251 | ||||||
| chr6:131234483
|
G | C | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+14675G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234483 | ||||||
| chr6:131234509
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.850+14701C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234509 | ||||||
| chr6:131234519
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0002g0288 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.850+14711G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234519 | ||||||
| chr6:131234533
|
G | C | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+14725G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234533 | ||||||
| chr6:131234710
|
A | G | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+14902A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234710 | ||||||
| chr6:131234804
|
C | T | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+14996C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234804 | ||||||
| chr6:131235055
|
C | G | 1 | a0001c0001t0003g0052 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850+15247C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235055 | ||||||
| chr6:131235240
|
T | C | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+15432T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235240 | ||||||
| chr6:131235255
|
A | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+15447A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235255 | ||||||
| chr6:131235319
|
T | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+15511T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235319 | ||||||
| chr6:131235377
|
A | G | 3 | a0001c0001t0001g0225a0002c0002t0020g0149a0006c0006t0035g0217 | 3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.850+15569A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235377 | ||||||
| chr6:131235398
|
T | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0191 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.850+15590T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235398 | ||||||
| chr6:131235616
|
T | C | 55 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.850+15808T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235616 | ||||||
| chr6:131235636
|
T | G | 1 | a0001c0001t0010g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+15828T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235636 | ||||||
| chr6:131235710
|
T | C | 2 | a0001c0001t0021g0223a0001c0001t0022g0095 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.850+15902T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235710 | ||||||
| chr6:131236063
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.850+16255A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236063 | ||||||
| chr6:131236065
|
T | G | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+16257T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236065 | ||||||
| chr6:131236117
|
A | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+16309A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236117 | ||||||
| chr6:131236165
|
G | C | 172 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(169): Show | 172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.850+16357G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236165 | ||||||
| chr6:131236249
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+16441G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236249 | ||||||
| chr6:131236287
|
A | G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.850+16479A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236287 | ||||||
| chr6:131236295
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.850+16487T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236295 | ||||||
| chr6:131236323
|
C | T | 65 | a0001c0001t0001g0083a0001c0001t0001g0115a0001c0001t0001g0118others(62): Show | 65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.850+16515C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236323 | ||||||
| chr6:131236324
|
G | A | 1 | a0001c0001t0005g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850+16516G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236324 | ||||||
| chr6:131236377
|
T | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850+16569T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236377 | ||||||
| chr6:131236431
|
G | A | 1 | a0003c0003t0008g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850+16623G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236431 | ||||||
| chr6:131236483
|
A | T | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+16675A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236483 | ||||||
| chr6:131236852
|
C | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+17044C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236852 | ||||||
| chr6:131236919
|
C | G | 50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.850+17111C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236919 | ||||||
| chr6:131236921
|
G | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+17113G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236921 | ||||||
| chr6:131236922
|
G | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+17114G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236922 | ||||||
| chr6:131236937
|
A | G | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+17129A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236937 | ||||||
| chr6:131236975
|
T | C | 3 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0055 | 3 | NA18943.hp1 NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.850+17167T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236975 | ||||||
| chr6:131237076
|
G | T | 1 | a0002c0002t0002g0273 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.850+17268G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237076 | ||||||
| chr6:131237104
|
T | G | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+17296T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237104 | ||||||
| chr6:131237117
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0170 | 3 | HG01074.hp1 HG01169.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.850+17309G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237117 | ||||||
| chr6:131237453
|
A | G | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+17645A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237453 | ||||||
| chr6:131237514
|
C | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+17706C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237514 | ||||||
| chr6:131237550
|
T | A | 1 | a0001c0001t0022g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850+17742T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237550 | ||||||
| chr6:131237584
|
G | A | 4 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0004g0205others(1): Show | 4 | NA18946.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+17776G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237584 | ||||||
| chr6:131237586
|
C | T | 4 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0004g0205others(1): Show | 4 | NA18946.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+17778C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237586 | ||||||
| chr6:131237612
|
A | G | 18 | a0001c0001t0004g0059a0001c0001t0004g0168a0001c0001t0004g0169others(15): Show | 18 | HG00408.hp2 HG01993.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.850+17804A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237612 | ||||||
| chr6:131237669
|
C | G | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+17861C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237669 | ||||||
| chr6:131237738
|
G | A | 2 | a0001c0001t0007g0243a0001c0001t0009g0221 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+17930G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237738 | ||||||
| chr6:131237759
|
C | T | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+17951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237759 | ||||||
| chr6:131237826
|
A | G | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.850+18018A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237826 | ||||||
| chr6:131237852
|
A | T | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18044A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237852 | ||||||
| chr6:131237926
|
G | A | 20 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.850+18118G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237926 | ||||||
| chr6:131237956
|
T | C | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850+18148T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237956 | ||||||
| chr6:131238302
|
T | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+18494T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238302 | ||||||
| chr6:131238327
|
T | C | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+18519T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238327 | ||||||
| chr6:131238431
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0123 | 2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.850+18623G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238431 | ||||||
| chr6:131238446
|
G | A | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+18638G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238446 | ||||||
| chr6:131238654
|
T | C | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18846T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238654 | ||||||
| chr6:131238661
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850+18853T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238661 | ||||||
| chr6:131238684
|
C | A | 1 | a0002c0002t0003g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.850+18876C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238684 | ||||||
| chr6:131238684
|
C | G | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+18876C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238684 | ||||||
| chr6:131238742
|
T | C | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18934T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238742 | ||||||
| chr6:131238842
|
A | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.850+19034A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238842 | ||||||
| chr6:131238844
|
G | A | 1 | a0002c0002t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.850+19036G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238844 | ||||||
| chr6:131238873
|
C | T | 2 | a0001c0001t0025g0066a0002c0002t0003g0108 | 2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.850+19065C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238873 | ||||||
| chr6:131239089
|
T | G | 2 | a0001c0001t0007g0282a0001c0001t0028g0236 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850+19281T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239089 | ||||||
| chr6:131239129
|
C | A | 1 | a0001c0001t0033g0100 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.850+19321C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239129 | ||||||
| chr6:131239233
|
G | A | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+19425G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239233 | ||||||
| chr6:131239266
|
C | T | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+19458C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239266 | ||||||
| chr6:131239314
|
A | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.850+19506A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239314 | ||||||
| chr6:131239358
|
A | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+19550A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239358 | ||||||
| chr6:131239419
|
C | T | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+19611C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239419 | ||||||
| chr6:131239420
|
G | A | 1 | a0001c0001t0007g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.850+19612G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239420 | ||||||
| chr6:131239449
|
T | G | 126 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0001g0225others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.850+19641T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239449 | ||||||
| chr6:131239463
|
G | T | 1 | a0001c0001t0003g0056 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.850+19655G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239463 | ||||||
| chr6:131239468
|
G | A | 43 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.850+19660G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239468 | ||||||
| chr6:131239513
|
G | T | 2 | a0001c0001t0007g0243a0001c0001t0009g0221 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+19705G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239513 | ||||||
| chr6:131239556
|
G | T | 2 | a0001c0001t0021g0223a0001c0001t0022g0095 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.850+19748G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239556 | ||||||
| chr6:131239588
|
T | C | 3 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184 | 3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.850+19780T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239588 | ||||||
| chr6:131239722
|
G | A | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+19914G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239722 | ||||||
| chr6:131239735
|
C | T | 1 | a0001c0001t0004g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.850+19927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239735 | ||||||
| chr6:131239738
|
G | T | 2 | a0006c0006t0014g0003a0006c0006t0014g0004 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+19930G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239738 | ||||||
| chr6:131239876
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.850+20068T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239876 | ||||||
| chr6:131239907
|
T | C | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+20099T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239907 | ||||||
| chr6:131239927
|
C | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0133 | 2 | HG02004.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.850+20119C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239927 | ||||||
| chr6:131239979
|
C | T | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+20171C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239979 | ||||||
| chr6:131240068
|
C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850+20260C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240068 | ||||||
| chr6:131240141
|
T | C | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+20333T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240141 | ||||||
| chr6:131240204
|
G | A | 2 | a0001c0001t0004g0203a0001c0001t0004g0204 | 2 | NA18941.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.850+20396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240204 | ||||||
| chr6:131240221
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0151others(2): Show | 5 | HG01074.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+20413G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240221 | ||||||
| chr6:131240233
|
A | C | 2 | a0001c0001t0007g0282a0001c0001t0028g0236 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850+20425A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240233 | ||||||
| chr6:131240300
|
G | A | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+20492G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240300 | ||||||
| chr6:131240491
|
C | A | 2 | a0002c0002t0001g0135a0002c0002t0001g0136 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.850+20683C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240491 | ||||||
| chr6:131240514
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.850+20706A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240514 | ||||||
| chr6:131240522
|
A | T | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.850+20714A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240522 | ||||||
| chr6:131240699
|
G | A | 1 | a0002c0002t0036g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850+20891G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240699 | ||||||
| chr6:131240702
|
G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+20894G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240702 | ||||||
| chr6:131240799
|
G | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0077 | 2 | HG02486.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.850+20991G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240799 | ||||||
| chr6:131240856
|
G | A | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+21048G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240856 | ||||||
| chr6:131240889
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850+21081C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240889 | ||||||
| chr6:131240890
|
G | A | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+21082G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240890 | ||||||
| chr6:131240942
|
C | T | 5 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+21134C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240942 | ||||||
| chr6:131241161
|
T | C | 1 | a0001c0001t0003g0043 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.850+21353T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241161 | ||||||
| chr6:131241382
|
A | T | 1 | a0006c0006t0014g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850+21574A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241382 | ||||||
| chr6:131241437
|
C | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+21629C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241437 | ||||||
| chr6:131241451
|
A | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.850+21643A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241451 | ||||||
| chr6:131241525
|
G | C | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+21717G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241525 | ||||||
| chr6:131241569
|
T | TTA | 3 | a0004c0004t0001g0001a0004c0004t0001g0216a0004c0004t0003g0167 | 4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21769_850+2177 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | |||||
| chr6:131241569
|
T | TTATA | 16 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(13): Show | 16 | HG01175.hp2 HG01192.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.850+21767_850+2177 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | |||||
| chr6:131241569
|
T | TTATATA | 4 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0003g0048others(1): Show | 4 | HG00323.hp1 HG01981.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21765_850+2177 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | |||||
| chr6:131241577
|
A | ATG | 21 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(18): Show | 21 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.850+21819_850+2182 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
A | ATGTG | 14 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0138others(11): Show | 14 | HG01169.hp1 HG01952.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+21817_850+2182 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
A | ATGTGTG | 8 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0087others(5): Show | 8 | HG02145.hp1 HG02486.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.850+21815_850+2182 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.850+21811_850+2182 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
A | G | 6 | a0001c0001t0003g0064a0001c0001t0041g0158a0005c0005t0005g0097others(3): Show | 6 | HG00558.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21769A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241577 | ||||||
| chr6:131241577
|
ATG | A | 32 | a0001c0001t0001g0078a0001c0001t0001g0112a0001c0001t0001g0125others(29): Show | 32 | HG00544.hp2 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.850+21819_850+2182 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
ATGTG | A | 6 | a0001c0001t0001g0104a0001c0001t0002g0234a0001c0001t0002g0279others(3): Show | 6 | HG00099.hp2 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21817_850+2182 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241577
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+21809_850+2182 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | |||||
| chr6:131241579
|
G | A | 40 | a0001c0001t0001g0083a0001c0001t0002g0248a0001c0001t0003g0072others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.850+21771G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241579 | ||||||
| chr6:131241581
|
G | A | 4 | a0002c0002t0001g0121a0002c0002t0001g0177a0002c0002t0002g0265others(1): Show | 4 | HG01109.hp2 HG02074.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21773G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241581 | ||||||
| chr6:131241599
|
G | GTGTGTGT others(29): Show |
1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.850+21814_850+2181 others(40): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | |||||
| chr6:131241599
|
G | GTGTGTGT others(31): Show |
4 | a0001c0001t0004g0204a0001c0001t0006g0002a0001c0001t0011g0163others(1): Show | 4 | HG02572.hp1 NA18941.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21816_850+2181 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | |||||
| chr6:131241599
|
G | GTGTGTGT others(33): Show |
2 | a0001c0001t0005g0092a0001c0001t0007g0277 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.850+21818_850+2181 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | |||||
| chr6:131241601
|
G | GTGTGTGT others(49): Show |
1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+21808_850+2180 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241601 | |||||
| chr6:131241601
|
G | GTGTGTGT others(55): Show |
2 | a0006c0006t0014g0003a0006c0006t0014g0004 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+21814_850+2181 others(66): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241601 | |||||
| chr6:131241607
|
G | GTATATAT others(15): Show |
21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+21800_850+2180 others(26): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241607 | |||||
| chr6:131241607
|
G | GTGTGTGT others(17): Show |
1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+21808_850+2180 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241607 | |||||
| chr6:131241609
|
GTGTGTGT others(13): Show |
G | 4 | a0001c0001t0021g0220a0001c0001t0021g0223a0001c0001t0022g0085others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21803_850+2182 others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241609 | |||||
| chr6:131241611
|
GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184 | 3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.850+21805_850+2182 others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241611 | |||||
| chr6:131241616
|
TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.850+21809_850+2181 others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241616 | ||||||
| chr6:131241623
|
G | GTATATAT others(3): Show |
19 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.850+21816_850+2181 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241623 | |||||
| chr6:131241623
|
G | GTATATAT others(5): Show |
1 | a0002c0002t0002g0235 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.850+21816_850+2181 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241623 | |||||
| chr6:131241625
|
G | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0004g0204others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.850+21817G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241625 | ||||||
| chr6:131241625
|
G | GTATACGT others(31): Show |
1 | a0002c0002t0024g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+21818_850+2181 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | |||||
| chr6:131241625
|
G | GTATACGT others(33): Show |
6 | a0001c0001t0001g0045a0001c0001t0002g0261a0001c0001t0002g0275others(3): Show | 6 | HG02155.hp2 HG02293.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21818_850+2181 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | |||||
| chr6:131241625
|
G | GTATACGT others(59): Show |
1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+21818_850+2181 others(70): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | |||||
| chr6:131241625
|
G | GTATATAC others(61): Show |
1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+21818_850+2181 others(72): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | |||||
| chr6:131241625
|
G | GTATATAT others(41): Show |
1 | a0005c0005t0011g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.850+21818_850+2181 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | |||||
| chr6:131241627
|
G | A | 58 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0083others(55): Show | 58 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.850+21819G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241627 | ||||||
| chr6:131241627
|
G | GTATACGT others(31): Show |
2 | a0001c0001t0007g0243a0001c0001t0009g0221 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+21823_850+2182 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATACGT others(33): Show |
2 | a0001c0001t0005g0156a0001c0001t0005g0224 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+21823_850+2182 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATACGT others(35): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0003g0040others(7): Show | 10 | HG00280.hp1 HG01993.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+21823_850+2182 others(46): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATACGT others(61): Show |
1 | a0003c0003t0032g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.850+21823_850+2182 others(72): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATATAC others(41): Show |
1 | a0002c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.850+21825_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATATAT others(43): Show |
5 | a0002c0002t0001g0121a0002c0002t0001g0177a0002c0002t0002g0265others(2): Show | 5 | HG01109.hp2 HG02074.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+21827_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTATATAT others(43): Show |
3 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099 | 3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.850+21827_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTATAC others(35): Show |
2 | a0002c0002t0015g0008a0002c0002t0015g0009 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(46): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTATAC others(37): Show |
27 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0028others(24): Show | 27 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(48): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTATAT others(45): Show |
6 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0109others(3): Show | 6 | HG01192.hp2 HG01981.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(37): Show |
1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(48): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(39): Show |
23 | a0001c0001t0001g0013a0001c0001t0001g0123a0001c0001t0001g0126others(20): Show | 23 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(50): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(41): Show |
1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(45): Show |
1 | a0002c0002t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(47): Show |
4 | a0002c0002t0001g0106a0002c0002t0001g0120a0002c0002t0002g0273others(1): Show | 4 | HG00323.hp1 HG01175.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTAT others(47): Show |
1 | a0005c0005t0011g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(39): Show |
2 | a0001c0001t0007g0281a0001c0001t0040g0080 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(50): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(41): Show |
10 | a0001c0001t0001g0031a0001c0001t0002g0267a0001c0001t0003g0047others(7): Show | 10 | HG00544.hp1 HG01943.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(47): Show |
1 | a0001c0001t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0002c0002t0001g0114 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(53): Show |
1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(43): Show |
3 | a0001c0001t0001g0012a0001c0001t0004g0201a0001c0001t0006g0291 | 3 | HG01433.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0006c0006t0035g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0002c0002t0017g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(45): Show |
1 | a0001c0001t0005g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(51): Show |
1 | a0002c0002t0002g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(62): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(47): Show |
1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(43): Show |
1 | a0001c0001t0007g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(45): Show |
4 | a0001c0001t0001g0018a0001c0001t0004g0033a0001c0001t0004g0178others(1): Show | 4 | HG01099.hp1 NA18970.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(53): Show |
1 | a0002c0002t0036g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0002c0002t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(47): Show |
1 | a0007c0011t0004g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(53): Show |
1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
2 | a0001c0001t0005g0076a0001c0001t0009g0101 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(55): Show |
1 | a0002c0002t0001g0229 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(66): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(47): Show |
1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(49): Show |
1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(57): Show |
1 | a0002c0002t0017g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(68): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241627
|
G | GTGTGTGT others(51): Show |
1 | a0001c0001t0005g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(62): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | |||||
| chr6:131241629
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0003g0142a0001c0001t0003g0150others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21821A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241629 | ||||||
| chr6:131241836
|
A | T | 2 | a0001c0001t0005g0156a0001c0001t0007g0251 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+22028A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241836 | ||||||
| chr6:131242137
|
A | G | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+22329A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242137 | ||||||
| chr6:131242152
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.850+22344A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242152 | ||||||
| chr6:131242226
|
G | A | 2 | a0001c0001t0005g0156a0001c0001t0007g0251 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+22418G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242226 | ||||||
| chr6:131242376
|
A | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+22568A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242376 | ||||||
| chr6:131242437
|
G | A | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+22629G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242437 | ||||||
| chr6:131242648
|
C | T | 56 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+22840C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242648 | ||||||
| chr6:131242672
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.850+22864C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242672 | ||||||
| chr6:131242810
|
A | G | 5 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+23002A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242810 | ||||||
| chr6:131242982
|
ATTTAGAG others(17): Show |
A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+23180_850+2320 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131242982 | |||||
| chr6:131243225
|
C | T | 2 | a0002c0002t0001g0229a0002c0002t0002g0302 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.850+23417C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243225 | ||||||
| chr6:131243451
|
A | T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+23643A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243451 | ||||||
| chr6:131243511
|
A | T | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.850+23703A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243511 | ||||||
| chr6:131243653
|
C | T | 1 | a0003c0003t0008g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850+23845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243653 | ||||||
| chr6:131243726
|
T | C | 12 | a0001c0001t0008g0218a0001c0001t0010g0081a0001c0001t0010g0185others(9): Show | 12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.850+23918T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243726 | ||||||
| chr6:131243958
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.850+24150A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243958 | ||||||
| chr6:131243970
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.850+24162C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243970 | ||||||
| chr6:131243999
|
C | CT | 83 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0002g0238others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.850+24204dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131243999 | |||||
| chr6:131243999
|
CT | C | 8 | a0002c0002t0015g0008a0002c0002t0015g0009a0002c0002t0024g0160others(5): Show | 9 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+24204delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131243999 | |||||
| chr6:131244011
|
T | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.850+24203T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244011 | ||||||
| chr6:131244013
|
C | T | 61 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.850+24205C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244013 | ||||||
| chr6:131244323
|
G | A | 4 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+24515G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244323 | ||||||
| chr6:131244327
|
A | G | 1 | a0001c0001t0022g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.850+24519A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244327 | ||||||
| chr6:131244620
|
A | G | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+24812A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244620 | ||||||
| chr6:131244657
|
G | C | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.850+24849G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244657 | ||||||
| chr6:131244708
|
G | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+24900G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244708 | ||||||
| chr6:131244743
|
T | C | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.850+24935T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244743 | ||||||
| chr6:131244777
|
T | A | 17 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(14): Show | 17 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.850+24969T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244777 | ||||||
| chr6:131244822
|
G | T | 63 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+25014G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244822 | ||||||
| chr6:131244836
|
GA | G | 9 | a0001c0001t0005g0156a0001c0001t0007g0251a0002c0002t0001g0090others(6): Show | 9 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.850+25037delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131244836 | |||||
| chr6:131245402
|
G | T | 2 | a0001c0001t0023g0174a0001c0001t0023g0175 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.850+25594G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245402 | ||||||
| chr6:131245412
|
G | GT | 11 | a0001c0001t0001g0019a0001c0001t0002g0258a0001c0001t0002g0272others(8): Show | 11 | HG00609.hp2 HG01081.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+25615dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245412 | |||||
| chr6:131245412
|
GT | G | 55 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0031g0285others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.850+25615delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245412 | |||||
| chr6:131245423
|
T | G | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+25615T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245423 | ||||||
| chr6:131245424
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+25616G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245424 | ||||||
| chr6:131245439
|
G | GT | 7 | a0001c0001t0002g0247a0003c0003t0010g0082a0005c0005t0005g0097others(4): Show | 7 | HG00597.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+25642dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245439 | |||||
| chr6:131245440
|
T | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+25632T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245440 | ||||||
| chr6:131245458
|
T | C | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+25650T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245458 | ||||||
| chr6:131245468
|
G | A | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+25660G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245468 | ||||||
| chr6:131245523
|
C | T | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+25715C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245523 | ||||||
| chr6:131245591
|
G | A | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.850+25783G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245591 | ||||||
| chr6:131245631
|
C | T | 6 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(3): Show | 6 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+25823C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245631 | ||||||
| chr6:131245644
|
A | T | 3 | a0001c0001t0013g0202a0001c0001t0013g0210a0001c0001t0030g0294 | 3 | NA18969.hp1 NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.850+25836A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245644 | ||||||
| chr6:131245747
|
G | A | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.850+25939G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245747 | ||||||
| chr6:131245859
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850+26051C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245859 | ||||||
| chr6:131245883
|
T | C | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+26075T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245883 | ||||||
| chr6:131245905
|
C | T | 1 | a0002c0002t0039g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.850+26097C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245905 | ||||||
| chr6:131245934
|
A | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+26126A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245934 | ||||||
| chr6:131246009
|
C | T | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+26201C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246009 | ||||||
| chr6:131246056
|
A | T | 56 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+26248A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246056 | ||||||
| chr6:131246074
|
T | G | 23 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+26266T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246074 | ||||||
| chr6:131246094
|
A | AAT | 22 | a0001c0001t0001g0024a0001c0001t0001g0104a0001c0001t0001g0107others(19): Show | 22 | HG00558.hp1 HG01109.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.850+26309_850+2631 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | |||||
| chr6:131246094
|
A | AATAT | 6 | a0001c0001t0004g0036a0001c0001t0004g0207a0002c0002t0001g0093others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+26307_850+2631 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | |||||
| chr6:131246094
|
AAT | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0087a0001c0001t0001g0088others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.850+26309_850+2631 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | |||||
| chr6:131246101
|
A | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.850+26293A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246101 | ||||||
| chr6:131246525
|
T | C | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.850+26717T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246525 | ||||||
| chr6:131246648
|
G | A | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+26840G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246648 | ||||||
| chr6:131246962
|
A | AC | 82 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.850+27154_850+2715 others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246962 | ||||||
| chr6:131247269
|
G | GTA | 11 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0107others(8): Show | 12 | HG01071.hp2 HG01109.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+27505_850+2750 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTATA | 5 | a0001c0001t0001g0103a0001c0001t0002g0287a0001c0001t0003g0062others(2): Show | 5 | HG01106.hp1 HG01255.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+27503_850+2750 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTATATA | 4 | a0001c0001t0001g0031a0001c0001t0002g0248a0001c0001t0004g0197others(1): Show | 4 | HG00140.hp1 NA18963.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27501_850+2750 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0019a0001c0001t0002g0264a0001c0001t0026g0122others(2): Show | 5 | HG00099.hp1 HG00609.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+27499_850+2750 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0034a0001c0001t0001g0118a0001c0001t0002g0268 | 3 | HG03704.hp1 NA18942.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.850+27497_850+2750 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850+27493_850+2750 others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850+27462_850+2746 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTA | G | 27 | a0001c0001t0001g0129a0001c0001t0001g0151a0001c0001t0001g0192others(24): Show | 27 | HG00323.hp2 HG00609.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.850+27505_850+2750 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATA | G | 31 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0032others(28): Show | 31 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.850+27503_850+2750 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATA | G | 33 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.850+27501_850+2750 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(1): Show |
G | 17 | a0001c0001t0001g0025a0001c0001t0001g0170a0001c0001t0002g0238others(14): Show | 17 | HG01074.hp1 HG01169.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.850+27499_850+2750 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0014a0001c0001t0005g0094a0001c0001t0007g0286others(2): Show | 5 | HG02004.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+27497_850+2750 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(5): Show |
G | 7 | a0001c0001t0003g0058a0001c0001t0023g0174a0001c0001t0023g0175others(4): Show | 7 | HG01071.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+27495_850+2750 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(7): Show |
G | 34 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0131others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.850+27493_850+2750 others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(9): Show |
G | 39 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.850+27491_850+2750 others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(11): Show |
G | 10 | a0001c0001t0002g0234a0001c0001t0005g0092a0001c0001t0005g0224others(7): Show | 10 | HG01884.hp2 HG02074.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+27489_850+2750 others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(13): Show |
G | 18 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(15): Show | 18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850+27487_850+2750 others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(15): Show |
G | 4 | a0001c0001t0001g0225a0002c0002t0020g0149a0002c0002t0037g0162others(1): Show | 4 | HG03209.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27485_850+2750 others(26): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(17): Show |
G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+27483_850+2750 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(19): Show |
G | 7 | a0003c0003t0008g0143a0003c0003t0008g0144a0003c0003t0008g0145others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+27481_850+2750 others(30): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0020g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850+27479_850+2750 others(32): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247269
|
GTATATAT others(23): Show |
G | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.850+27477_850+2750 others(34): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | |||||
| chr6:131247271
|
A | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(5): Show | 8 | HG01981.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+27463A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247271 | ||||||
| chr6:131247275
|
A | G | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.850+27467A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247275 | ||||||
| chr6:131247277
|
A | G | 2 | a0001c0001t0004g0195a0005c0005t0011g0139 | 2 | HG02109.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.850+27469A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247277 | ||||||
| chr6:131247279
|
A | G | 6 | a0001c0001t0002g0256a0001c0001t0005g0074a0001c0001t0005g0075others(3): Show | 6 | HG01496.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+27471A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247279 | ||||||
| chr6:131247281
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.850+27473A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247281 | ||||||
| chr6:131247283
|
A | G | 4 | a0001c0001t0003g0058a0002c0002t0001g0096a0002c0002t0002g0245others(1): Show | 4 | HG01071.hp1 HG01081.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+27475A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247283 | ||||||
| chr6:131247285
|
A | G | 29 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0131others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.850+27477A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247285 | ||||||
| chr6:131247287
|
A | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 34 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.850+27479A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247287 | ||||||
| chr6:131247289
|
A | G | 3 | a0001c0001t0003g0105a0002c0002t0001g0177a0002c0002t0002g0265 | 3 | HG02074.hp2 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.850+27481A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247289 | ||||||
| chr6:131247291
|
A | G | 18 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(15): Show | 18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850+27483A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247291 | ||||||
| chr6:131247292
|
TATATATA others(16): Show |
T | 5 | a0001c0001t0031g0285a0003c0003t0032g0301a0006c0006t0014g0003others(2): Show | 5 | HG01891.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+27485_850+2750 others(27): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247292 | ||||||
| chr6:131247293
|
A | G | 4 | a0001c0001t0001g0225a0002c0002t0020g0149a0002c0002t0037g0162others(1): Show | 4 | HG03209.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27485A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247293 | ||||||
| chr6:131247294
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+27487_850+2750 others(25): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247294 | ||||||
| chr6:131247316
|
T | G | 7 | a0001c0001t0009g0184a0001c0001t0031g0285a0001c0001t0038g0166others(4): Show | 7 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+27508T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247316 | ||||||
| chr6:131247344
|
G | T | 2 | a0006c0006t0014g0003a0006c0006t0014g0004 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+27536G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247344 | ||||||
| chr6:131247453
|
G | C | 10 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+27645G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247453 | ||||||
| chr6:131247515
|
G | A | 1 | a0001c0001t0022g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850+27707G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247515 | ||||||
| chr6:131247558
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.850+27750G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247558 | ||||||
| chr6:131247653
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.850+27845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247653 | ||||||
| chr6:131247698
|
A | G | 25 | a0001c0001t0001g0083a0001c0001t0005g0074a0001c0001t0005g0075others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.850+27890A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247698 | ||||||
| chr6:131247784
|
T | C | 179 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.850+27976T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247784 | ||||||
| chr6:131248596
|
A | G | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+28788A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248596 | ||||||
| chr6:131248698
|
T | C | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+28890T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248698 | ||||||
| chr6:131248938
|
C | G | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+29130C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248938 | ||||||
| chr6:131248968
|
A | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+29160A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248968 | ||||||
| chr6:131249113
|
A | C | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+29305A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249113 | ||||||
| chr6:131249130
|
A | G | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+29322A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249130 | ||||||
| chr6:131249364
|
A | T | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+29556A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249364 | ||||||
| chr6:131249556
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0003g0071 | 2 | HG01943.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.850+29748G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249556 | ||||||
| chr6:131249601
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.850+29793A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249601 | ||||||
| chr6:131249924
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30116G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249924 | ||||||
| chr6:131250008
|
A | G | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+30200A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250008 | ||||||
| chr6:131250129
|
G | T | 45 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0004g0168others(42): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.850+30321G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250129 | ||||||
| chr6:131250245
|
G | A | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30437G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250245 | ||||||
| chr6:131250270
|
A | T | 1 | a0001c0001t0003g0056 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.850+30462A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250270 | ||||||
| chr6:131250276
|
T | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+30468T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250276 | ||||||
| chr6:131250418
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.850+30610G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250418 | ||||||
| chr6:131250548
|
A | G | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30740A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250548 | ||||||
| chr6:131250591
|
T | C | 1 | a0001c0001t0010g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+30783T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250591 | ||||||
| chr6:131251028
|
T | C | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-30502T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251028 | ||||||
| chr6:131251107
|
A | G | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.851-30423A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251107 | ||||||
| chr6:131251207
|
G | T | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-30323G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251207 | ||||||
| chr6:131251270
|
G | T | 2 | a0001c0001t0006g0002a0008c0008t0006g0002 | 2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.851-30260G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251270 | ||||||
| chr6:131251498
|
G | A | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851-30032G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251498 | ||||||
| chr6:131251568
|
T | TA | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(160): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.851-29952dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131251568 | |||||
| chr6:131251637
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.851-29893G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251637 | ||||||
| chr6:131251738
|
T | C | 3 | a0001c0001t0005g0094a0001c0001t0007g0286a0009c0009t0005g0230 | 3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-29792T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251738 | ||||||
| chr6:131251959
|
G | A | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-29571G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251959 | ||||||
| chr6:131252024
|
C | T | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-29506C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252024 | ||||||
| chr6:131252156
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.851-29374T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252156 | ||||||
| chr6:131252293
|
A | G | 196 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(193): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.851-29237A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252293 | ||||||
| chr6:131252601
|
G | A | 1 | a0001c0001t0003g0051 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.851-28929G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252601 | ||||||
| chr6:131252732
|
A | T | 60 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.851-28798A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252732 | ||||||
| chr6:131252770
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.851-28760T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252770 | ||||||
| chr6:131252822
|
G | A | 1 | a0002c0002t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.851-28708G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252822 | ||||||
| chr6:131253135
|
T | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.851-28395T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253135 | ||||||
| chr6:131253246
|
A | AT | 14 | a0001c0001t0005g0156a0001c0001t0005g0224a0001c0001t0007g0243others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-28277dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253246 | |||||
| chr6:131253347
|
G | A | 48 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 48 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.851-28183G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253347 | ||||||
| chr6:131253351
|
T | C | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851-28179T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253351 | ||||||
| chr6:131253357
|
T | C | 2 | a0001c0001t0023g0174a0001c0001t0023g0175 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851-28173T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253357 | ||||||
| chr6:131253586
|
T | G | 1 | a0001c0001t0003g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.851-27944T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253586 | ||||||
| chr6:131253659
|
C | CTTAT | 43 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0078others(40): Show | 43 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-27838_851-2783 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | |||||
| chr6:131253659
|
C | CTTATTTA others(1): Show |
9 | a0001c0001t0002g0293a0001c0001t0002g0297a0001c0001t0004g0026others(6): Show | 9 | HG00544.hp2 HG01943.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-27842_851-2783 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | |||||
| chr6:131253659
|
CTTATTTA others(1): Show |
C | 95 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.851-27842_851-2783 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | |||||
| chr6:131253659
|
CTTATTTA others(5): Show |
C | 14 | a0001c0001t0005g0092a0001c0001t0005g0156a0001c0001t0005g0224others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-27846_851-2783 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | |||||
| chr6:131253659
|
CTTATTTA others(9): Show |
C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-27850_851-2783 others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | |||||
| chr6:131253929
|
G | A | 50 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-27601G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253929 | ||||||
| chr6:131254052
|
T | A | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-27478T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254052 | ||||||
| chr6:131254128
|
CTG | C | 11 | a0001c0001t0008g0218a0001c0001t0010g0185a0001c0001t0023g0174others(8): Show | 11 | HG02559.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.851-27400_851-2739 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131254128 | |||||
| chr6:131254210
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0125a0001c0001t0001g0176others(5): Show | 8 | HG00408.hp1 HG02074.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-27320C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254210 | ||||||
| chr6:131254471
|
A | T | 3 | a0001c0001t0005g0094a0001c0001t0007g0286a0009c0009t0005g0230 | 3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-27059A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254471 | ||||||
| chr6:131254492
|
C | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-27038C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254492 | ||||||
| chr6:131254506
|
A | G | 1 | a0002c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851-27024A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254506 | ||||||
| chr6:131255088
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-26442A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255088 | ||||||
| chr6:131255487
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.851-26043C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255487 | ||||||
| chr6:131255498
|
A | C | 1 | a0001c0001t0041g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851-26032A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255498 | ||||||
| chr6:131255539
|
T | G | 55 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.851-25991T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255539 | ||||||
| chr6:131255844
|
C | T | 1 | a0001c0001t0040g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.851-25686C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255844 | ||||||
| chr6:131256047
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.851-25483G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256047 | ||||||
| chr6:131256061
|
C | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-25469C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256061 | ||||||
| chr6:131256162
|
A | G | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(159): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.851-25368A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256162 | ||||||
| chr6:131256191
|
G | A | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-25339G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256191 | ||||||
| chr6:131256551
|
T | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-24979T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256551 | ||||||
| chr6:131256624
|
T | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0125others(6): Show | 9 | HG00408.hp1 HG02074.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.851-24906T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256624 | ||||||
| chr6:131256629
|
G | A | 7 | a0002c0002t0001g0090a0002c0002t0001g0096a0002c0002t0002g0244others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-24901G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256629 | ||||||
| chr6:131256640
|
ACT | A | 46 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.851-24887_851-2488 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256640 | |||||
| chr6:131256649
|
T | C | 3 | a0001c0001t0001g0225a0002c0002t0020g0149a0006c0006t0035g0217 | 3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.851-24881T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256649 | ||||||
| chr6:131256653
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.851-24877G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256653 | ||||||
| chr6:131256708
|
C | CATT | 22 | a0001c0001t0001g0029a0001c0001t0001g0087a0001c0001t0001g0088others(19): Show | 22 | HG00408.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.851-24796_851-2479 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | |||||
| chr6:131256708
|
C | CATTATTA others(2): Show |
27 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.851-24802_851-2479 others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | |||||
| chr6:131256708
|
C | CATTATTA others(5): Show |
18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 18 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.851-24805_851-2479 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | |||||
| chr6:131256708
|
C | CATTATTA others(8): Show |
1 | a0001c0001t0003g0046 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.851-24808_851-2479 others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | |||||
| chr6:131256708
|
CATT | C | 95 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0004g0026others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.851-24796_851-2479 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | |||||
| chr6:131256752
|
CAGG | C | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24777_851-2477 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256752 | ||||||
| chr6:131256756
|
T | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24774T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256756 | ||||||
| chr6:131256780
|
T | G | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24750T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256780 | ||||||
| chr6:131256781
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24749C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256781 | ||||||
| chr6:131256782
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24748C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256782 | ||||||
| chr6:131256783
|
T | TGAGC | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24747_851-2474 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256783 | ||||||
| chr6:131256784
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24746C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256784 | ||||||
| chr6:131256786
|
C | A | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24744C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256786 | ||||||
| chr6:131256810
|
G | T | 2 | a0002c0002t0001g0120a0002c0002t0002g0288 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.851-24720G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256810 | ||||||
| chr6:131256945
|
C | CTTGAAAC others(10): Show |
44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24585_851-2458 others(21): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256945 | ||||||
| chr6:131256946
|
C | G | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24584C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256946 | ||||||
| chr6:131256947
|
C | A | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24583C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256947 | ||||||
| chr6:131257201
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.851-24329G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257201 | ||||||
| chr6:131257367
|
C | CA | 61 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(58): Show | 61 | HG00280.hp1 HG00558.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.851-24141dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | |||||
| chr6:131257367
|
C | CAA | 41 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0002g0267others(38): Show | 41 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.851-24142_851-2414 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | |||||
| chr6:131257367
|
CA | C | 49 | a0001c0001t0001g0019a0001c0001t0001g0083a0001c0001t0001g0225others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.851-24141delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | |||||
| chr6:131257367
|
CAA | C | 9 | a0001c0001t0005g0089a0002c0002t0001g0114a0002c0002t0001g0135others(6): Show | 9 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.851-24142_851-2414 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | |||||
| chr6:131257537
|
C | T | 50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.851-23993C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257537 | ||||||
| chr6:131257541
|
C | T | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-23989C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257541 | ||||||
| chr6:131257545
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.851-23985T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257545 | ||||||
| chr6:131257764
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0003g0056 | 3 | NA18962.hp2 NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.851-23766G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257764 | ||||||
| chr6:131258294
|
G | A | 44 | a0001c0001t0001g0031a0001c0001t0004g0026a0001c0001t0004g0033others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-23236G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131258294 | ||||||
| chr6:131258663
|
G | C | 4 | a0001c0001t0001g0045a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-22867G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131258663 | ||||||
| chr6:131259160
|
A | G | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-22370A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259160 | ||||||
| chr6:131259483
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.851-22047G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259483 | ||||||
| chr6:131259794
|
A | C | 1 | a0001c0001t0019g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.851-21736A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259794 | ||||||
| chr6:131259802
|
T | A | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-21728T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259802 | ||||||
| chr6:131259818
|
T | C | 2 | a0001c0001t0008g0218a0001c0001t0010g0185 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.851-21712T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259818 | ||||||
| chr6:131259828
|
C | A | 7 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184others(4): Show | 7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-21702C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259828 | ||||||
| chr6:131259920
|
G | A | 7 | a0001c0001t0002g0272a0001c0001t0031g0285a0001c0001t0038g0166others(4): Show | 7 | HG00741.hp1 HG01891.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-21610G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259920 | ||||||
| chr6:131259933
|
A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-21597A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259933 | ||||||
| chr6:131259949
|
G | GC | 61 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.851-21577dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131259949 | |||||
| chr6:131260000
|
A | C | 172 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(169): Show | 172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.851-21530A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260000 | ||||||
| chr6:131260072
|
G | A | 50 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-21458G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260072 | ||||||
| chr6:131260072
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-21458G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260072 | ||||||
| chr6:131260267
|
G | A | 3 | a0001c0001t0005g0156a0001c0001t0007g0251a0002c0002t0037g0162 | 3 | HG02486.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.851-21263G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260267 | ||||||
| chr6:131260488
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.851-21042C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260488 | ||||||
| chr6:131260577
|
A | C | 1 | a0001c0001t0016g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.851-20953A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260577 | ||||||
| chr6:131260729
|
A | T | 5 | a0002c0002t0001g0093a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-20801A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260729 | ||||||
| chr6:131260882
|
A | C | 57 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(54): Show | 57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-20648A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260882 | ||||||
| chr6:131260919
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-20611C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260919 | ||||||
| chr6:131260956
|
G | A | 6 | a0001c0001t0031g0285a0001c0001t0038g0166a0003c0003t0032g0301others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-20574G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260956 | ||||||
| chr6:131260994
|
T | C | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.851-20536T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260994 | ||||||
| chr6:131261042
|
CAA | C | 3 | a0001c0001t0005g0094a0001c0001t0007g0286a0009c0009t0005g0230 | 3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-20486_851-2048 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261042 | |||||
| chr6:131261057
|
G | A | 47 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-20473G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261057 | ||||||
| chr6:131261078
|
C | T | 3 | a0001c0001t0013g0202a0001c0001t0013g0210a0001c0001t0030g0294 | 3 | NA18969.hp1 NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.851-20452C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261078 | ||||||
| chr6:131261209
|
C | CA | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.851-20305dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261209 | |||||
| chr6:131261209
|
CA | C | 21 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(18): Show | 21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-20305delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261209 | |||||
| chr6:131261230
|
A | G | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-20300A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261230 | ||||||
| chr6:131261249
|
A | C | 1 | a0001c0001t0022g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.851-20281A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261249 | ||||||
| chr6:131261306
|
C | T | 12 | a0001c0001t0008g0218a0001c0001t0010g0081a0001c0001t0010g0185others(9): Show | 12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.851-20224C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261306 | ||||||
| chr6:131261317
|
CACTT | C | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-20210_851-2020 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261317 | |||||
| chr6:131261541
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.851-19989T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261541 | ||||||
| chr6:131261689
|
C | T | 43 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-19841C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261689 | ||||||
| chr6:131261690
|
G | A | 1 | a0004c0004t0003g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.851-19840G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261690 | ||||||
| chr6:131261761
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851-19769A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261761 | ||||||
| chr6:131261796
|
G | A | 46 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.851-19734G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261796 | ||||||
| chr6:131262330
|
G | C | 13 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0224others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.851-19200G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262330 | ||||||
| chr6:131262559
|
A | T | 1 | a0001c0001t0002g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.851-18971A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262559 | ||||||
| chr6:131262611
|
T | A | 47 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(44): Show | 47 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-18919T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262611 | ||||||
| chr6:131262612
|
T | A | 47 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(44): Show | 47 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-18918T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262612 | ||||||
| chr6:131262613
|
A | T | 2 | a0001c0001t0001g0153a0004c0004t0003g0167 | 2 | HG01099.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.851-18917A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262613 | ||||||
| chr6:131262616
|
A | AAT | 4 | a0001c0001t0031g0285a0001c0001t0038g0166a0006c0006t0014g0003others(1): Show | 4 | HG00741.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-18913_851-1891 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131262616 | |||||
| chr6:131262618
|
A | T | 108 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0004g0026others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.851-18912A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262618 | ||||||
| chr6:131262804
|
T | C | 2 | a0002c0002t0001g0135a0002c0002t0001g0136 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.851-18726T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262804 | ||||||
| chr6:131263192
|
A | G | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-18338A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263192 | ||||||
| chr6:131263325
|
G | A | 1 | a0002c0002t0003g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.851-18205G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263325 | ||||||
| chr6:131263508
|
T | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-18022T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263508 | ||||||
| chr6:131263670
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0041g0158a0002c0002t0001g0027others(22): Show | 25 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.851-17860G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263670 | ||||||
| chr6:131263776
|
A | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-17754A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263776 | ||||||
| chr6:131263832
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.851-17698C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263832 | ||||||
| chr6:131263833
|
G | A | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.851-17697G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263833 | ||||||
| chr6:131263986
|
T | G | 57 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(54): Show | 57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-17544T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263986 | ||||||
| chr6:131264009
|
A | G | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-17521A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264009 | ||||||
| chr6:131264102
|
G | A | 2 | a0002c0002t0017g0007a0002c0002t0036g0222 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.851-17428G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264102 | ||||||
| chr6:131264111
|
C | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-17419C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264111 | ||||||
| chr6:131264159
|
G | A | 57 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0089others(54): Show | 57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-17371G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264159 | ||||||
| chr6:131264361
|
A | G | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.851-17169A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264361 | ||||||
| chr6:131264515
|
A | G | 1 | a0001c0001t0010g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.851-17015A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264515 | ||||||
| chr6:131264571
|
CATAA | C | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-16951_851-1694 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131264571 | |||||
| chr6:131264587
|
T | G | 2 | a0001c0001t0001g0032a0001c0001t0002g0252 | 2 | NA18953.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.851-16943T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264587 | ||||||
| chr6:131264763
|
C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851-16767C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264763 | ||||||
| chr6:131265004
|
G | A | 5 | a0001c0001t0007g0243a0001c0001t0009g0221a0002c0002t0015g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-16526G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265004 | ||||||
| chr6:131265160
|
A | G | 18 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(15): Show | 18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.851-16370A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265160 | ||||||
| chr6:131265161
|
G | T | 18 | a0002c0002t0001g0027a0002c0002t0001g0067a0002c0002t0001g0106others(15): Show | 18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.851-16369G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265161 | ||||||
| chr6:131265403
|
G | A | 1 | a0001c0001t0010g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.851-16127G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265403 | ||||||
| chr6:131265694
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.851-15836A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265694 | ||||||
| chr6:131265795
|
A | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.851-15735A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265795 | ||||||
| chr6:131265847
|
C | T | 2 | a0002c0002t0003g0132a0002c0002t0003g0134 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.851-15683C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265847 | ||||||
| chr6:131265962
|
C | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-15568C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265962 | ||||||
| chr6:131266017
|
A | G | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.851-15513A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266017 | ||||||
| chr6:131266099
|
G | A | 1 | a0001c0001t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.851-15431G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266099 | ||||||
| chr6:131266173
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.851-15357T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266173 | ||||||
| chr6:131266684
|
TTTG | T | 4 | a0001c0001t0021g0220a0001c0001t0021g0223a0001c0001t0022g0085others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-14822_851-1482 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131266684 | |||||
| chr6:131266704
|
TG | T | 84 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.851-14825delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266704 | ||||||
| chr6:131266705
|
G | T | 59 | a0001c0001t0001g0023a0001c0001t0001g0083a0001c0001t0001g0225others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.851-14825G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266705 | ||||||
| chr6:131266708
|
G | T | 146 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.851-14822G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266708 | ||||||
| chr6:131266717
|
C | T | 4 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-14813C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266717 | ||||||
| chr6:131267064
|
C | CA | 61 | a0001c0001t0001g0083a0001c0001t0001g0225a0001c0001t0005g0074others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.851-14461dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131267064 | |||||
| chr6:131267442
|
G | A | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-14088G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267442 | ||||||
| chr6:131267573
|
A | C | 194 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(191): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.851-13957A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267573 | ||||||
| chr6:131267603
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-13927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267603 | ||||||
| chr6:131267936
|
A | G | 3 | a0001c0001t0002g0246a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.851-13594A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267936 | ||||||
| chr6:131267988
|
A | T | 1 | a0002c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.851-13542A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267988 | ||||||
| chr6:131268013
|
G | A | 4 | a0001c0001t0004g0059a0001c0001t0006g0254a0001c0001t0012g0060others(1): Show | 4 | HG01993.hp2 HG02293.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-13517G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268013 | ||||||
| chr6:131268032
|
G | T | 3 | a0001c0001t0002g0257a0001c0001t0002g0262a0001c0001t0002g0263 | 3 | NA18946.hp2 NA18955.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.851-13498G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268032 | ||||||
| chr6:131268097
|
G | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.851-13433G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268097 | ||||||
| chr6:131268102
|
T | A | 3 | a0002c0002t0017g0007a0002c0002t0017g0010a0002c0002t0036g0222 | 3 | HG02257.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.851-13428T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268102 | ||||||
| chr6:131268154
|
A | G | 16 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0156others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-13376A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268154 | ||||||
| chr6:131268155
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-13375A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268155 | ||||||
| chr6:131268173
|
T | C | 4 | a0001c0001t0034g0219a0002c0002t0015g0008a0002c0002t0015g0009others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-13357T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268173 | ||||||
| chr6:131268174
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.851-13356T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268174 | ||||||
| chr6:131268197
|
G | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0297 | 2 | NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.851-13333G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268197 | ||||||
| chr6:131268263
|
A | C | 1 | a0001c0001t0018g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.851-13267A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268263 | ||||||
| chr6:131268299
|
T | G | 21 | a0001c0001t0001g0083a0002c0002t0001g0063a0002c0002t0001g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-13231T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268299 | ||||||
| chr6:131268366
|
G | A | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.851-13164G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268366 | ||||||
| chr6:131268382
|
T | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0194others(3): Show | 6 | HG02155.hp1 NA18952.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-13148T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268382 | ||||||
| chr6:131268471
|
T | G | 3 | a0001c0001t0001g0225a0002c0002t0020g0149a0006c0006t0035g0217 | 3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.851-13059T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268471 | ||||||
| chr6:131268475
|
A | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-13055A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268475 | ||||||
| chr6:131268503
|
G | C | 4 | a0001c0001t0021g0220a0001c0001t0021g0223a0001c0001t0022g0085others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-13027G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268503 | ||||||
| chr6:131268572
|
A | G | 1 | a0001c0001t0004g0026 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.851-12958A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268572 | ||||||
| chr6:131268647
|
G | A | 15 | a0001c0001t0001g0129a0001c0001t0008g0218a0001c0001t0010g0081others(12): Show | 15 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.851-12883G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268647 | ||||||
| chr6:131268711
|
A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-12819A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268711 | ||||||
| chr6:131269247
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0003g0058 | 2 | HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.851-12283G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269247 | ||||||
| chr6:131269305
|
C | T | 7 | a0001c0001t0005g0089a0001c0001t0005g0092a0001c0001t0005g0224others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-12225C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269305 | ||||||
| chr6:131269327
|
C | T | 1 | a0001c0001t0010g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.851-12203C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269327 | ||||||
| chr6:131269588
|
A | G | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-11942A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269588 | ||||||
| chr6:131269626
|
G | A | 76 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(73): Show | 76 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-11904G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269626 | ||||||
| chr6:131269746
|
G | A | 4 | a0001c0001t0005g0092a0001c0001t0007g0277a0001c0001t0011g0163others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-11784G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269746 | ||||||
| chr6:131269789
|
A | G | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-11741A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269789 | ||||||
| chr6:131269817
|
A | T | 104 | a0001c0001t0001g0225a0001c0001t0003g0124a0001c0001t0004g0026others(101): Show | 104 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.851-11713A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269817 | ||||||
| chr6:131270053
|
C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-11477C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270053 | ||||||
| chr6:131270217
|
C | A | 1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.851-11313C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270217 | ||||||
| chr6:131270359
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851-11171C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270359 | ||||||
| chr6:131270360
|
G | A | 8 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-11170G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270360 | ||||||
| chr6:131270491
|
A | T | 1 | a0002c0002t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.851-11039A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270491 | ||||||
| chr6:131270845
|
A | G | 1 | a0002c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.851-10685A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270845 | ||||||
| chr6:131270967
|
A | G | 4 | a0001c0001t0038g0166a0006c0006t0014g0003a0006c0006t0014g0004others(1): Show | 4 | HG00741.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-10563A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270967 | ||||||
| chr6:131271227
|
T | A | 1 | a0001c0001t0004g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.851-10303T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271227 | ||||||
| chr6:131271255
|
GTTCT | G | 4 | a0001c0001t0021g0220a0001c0001t0021g0223a0001c0001t0022g0085others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-10272_851-1026 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131271255 | |||||
| chr6:131271379
|
C | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0194others(2): Show | 5 | HG02155.hp1 NA18952.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-10151C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271379 | ||||||
| chr6:131271386
|
T | G | 17 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0156others(14): Show | 17 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.851-10144T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271386 | ||||||
| chr6:131271423
|
T | C | 5 | a0004c0004t0001g0001a0004c0004t0001g0128a0004c0004t0001g0130others(2): Show | 6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-10107T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271423 | ||||||
| chr6:131271722
|
T | C | 24 | a0001c0001t0001g0225a0002c0002t0001g0027a0002c0002t0001g0067others(21): Show | 24 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.851-9808T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271722 | ||||||
| chr6:131271816
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.851-9714A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271816 | ||||||
| chr6:131271838
|
C | A | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-9692C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271838 | ||||||
| chr6:131271907
|
C | G | 66 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.851-9623C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271907 | ||||||
| chr6:131272010
|
A | G | 50 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-9520A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272010 | ||||||
| chr6:131272027
|
G | A | 1 | a0001c0001t0021g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.851-9503G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272027 | ||||||
| chr6:131272079
|
T | C | 22 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0156others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.851-9451T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272079 | ||||||
| chr6:131272277
|
A | G | 3 | a0002c0002t0001g0093a0002c0002t0001g0229a0002c0002t0002g0302 | 3 | HG02055.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.851-9253A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272277 | ||||||
| chr6:131272324
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.851-9206T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272324 | ||||||
| chr6:131272367
|
A | C | 4 | a0001c0001t0038g0166a0006c0006t0014g0003a0006c0006t0014g0004others(1): Show | 4 | HG00741.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-9163A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272367 | ||||||
| chr6:131272449
|
G | T | 2 | a0002c0002t0001g0177a0002c0002t0002g0265 | 2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.851-9081G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272449 | ||||||
| chr6:131272730
|
A | C | 1 | a0011c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-8800A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272730 | ||||||
| chr6:131272841
|
G | T | 1 | a0001c0001t0012g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.851-8689G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272841 | ||||||
| chr6:131272852
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8678T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272852 | ||||||
| chr6:131272864
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8666G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272864 | ||||||
| chr6:131273027
|
T | C | 4 | a0001c0001t0005g0156a0001c0001t0007g0251a0001c0001t0007g0282others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-8503T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273027 | ||||||
| chr6:131273096
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8434G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273096 | ||||||
| chr6:131273182
|
G | A | 9 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(6): Show | 9 | HG01978.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-8348G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273182 | ||||||
| chr6:131273239
|
C | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.851-8291C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273239 | ||||||
| chr6:131273488
|
T | G | 51 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(48): Show | 51 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(48): Show |
intron_variant | MODIFIER | c.851-8042T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273488 | ||||||
| chr6:131273606
|
C | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-7924C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273606 | ||||||
| chr6:131273722
|
C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-7808C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273722 | ||||||
| chr6:131273782
|
T | C | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-7748T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273782 | ||||||
| chr6:131273833
|
T | G | 1 | a0002c0002t0001g0114 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.851-7697T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273833 | ||||||
| chr6:131273940
|
CT | C | 45 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(42): Show | 45 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.851-7573delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131273940 | |||||
| chr6:131273988
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-7542G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273988 | ||||||
| chr6:131274168
|
C | G | 16 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0156others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-7362C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274168 | ||||||
| chr6:131274369
|
TCTTC | T | 4 | a0001c0001t0034g0219a0002c0002t0015g0008a0002c0002t0015g0009others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-7155_851-7152d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131274369 | |||||
| chr6:131274459
|
C | G | 50 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-7071C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274459 | ||||||
| chr6:131274496
|
T | G | 3 | a0001c0001t0005g0140a0001c0001t0009g0141a0001c0001t0009g0184 | 3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.851-7034T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274496 | ||||||
| chr6:131274498
|
T | C | 52 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(49): Show | 52 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(49): Show |
intron_variant | MODIFIER | c.851-7032T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274498 | ||||||
| chr6:131274897
|
ACT | A | 6 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-6630_851-6629d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131274897 | |||||
| chr6:131274912
|
G | A | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851-6618G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274912 | ||||||
| chr6:131275663
|
C | T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-5867C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131275663 | ||||||
| chr6:131275767
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.851-5763G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131275767 | ||||||
| chr6:131276014
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.851-5516C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276014 | ||||||
| chr6:131276180
|
A | G | 5 | a0005c0005t0005g0097a0005c0005t0005g0098a0005c0005t0005g0099others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-5350A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276180 | ||||||
| chr6:131276229
|
T | C | 41 | a0001c0001t0001g0225a0001c0001t0005g0092a0001c0001t0005g0140others(38): Show | 41 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.851-5301T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276229 | ||||||
| chr6:131276236
|
G | A | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.851-5294G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276236 | ||||||
| chr6:131276350
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.851-5180A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276350 | ||||||
| chr6:131276357
|
T | C | 50 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-5173T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276357 | ||||||
| chr6:131276534
|
A | G | 2 | a0001c0001t0006g0002a0008c0008t0006g0002 | 2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.851-4996A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276534 | ||||||
| chr6:131276539
|
A | G | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-4991A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276539 | ||||||
| chr6:131276753
|
C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-4777C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276753 | ||||||
| chr6:131276829
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.851-4701G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276829 | ||||||
| chr6:131276849
|
C | T | 72 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(69): Show | 72 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(69): Show |
intron_variant | MODIFIER | c.851-4681C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276849 | ||||||
| chr6:131276890
|
A | G | 2 | a0001c0001t0031g0285a0003c0003t0032g0301 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.851-4640A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276890 | ||||||
| chr6:131276976
|
A | G | 1 | a0002c0002t0001g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.851-4554A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276976 | ||||||
| chr6:131277048
|
T | A | 1 | a0001c0001t0005g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-4482T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277048 | ||||||
| chr6:131277151
|
G | A | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-4379G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277151 | ||||||
| chr6:131277543
|
G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-3987G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277543 | ||||||
| chr6:131277919
|
C | G | 14 | a0001c0001t0008g0218a0001c0001t0010g0081a0001c0001t0010g0185others(11): Show | 14 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.851-3611C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277919 | ||||||
| chr6:131278031
|
G | C | 10 | a0001c0001t0005g0089a0001c0001t0005g0094a0001c0001t0007g0286others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-3499G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278031 | ||||||
| chr6:131278046
|
G | A | 50 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-3484G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278046 | ||||||
| chr6:131278081
|
T | C | 10 | a0001c0001t0005g0089a0001c0001t0005g0094a0001c0001t0007g0286others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-3449T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278081 | ||||||
| chr6:131278181
|
G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-3349G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278181 | ||||||
| chr6:131278364
|
C | G | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.851-3166C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278364 | ||||||
| chr6:131278490
|
G | A | 76 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(73): Show | 76 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-3040G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278490 | ||||||
| chr6:131278546
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.851-2984T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278546 | ||||||
| chr6:131278582
|
A | G | 60 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(57): Show | 60 | HG00408.hp2 HG00597.hp1 HG01891.hp1 others(57): Show |
intron_variant | MODIFIER | c.851-2948A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278582 | ||||||
| chr6:131278912
|
G | A | 5 | a0001c0001t0005g0089a0001c0001t0005g0094a0001c0001t0007g0286others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-2618G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278912 | ||||||
| chr6:131279033
|
GT | G | 4 | a0001c0001t0021g0220a0001c0001t0021g0223a0001c0001t0022g0085others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-2494delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131279033 | |||||
| chr6:131279048
|
A | G | 169 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.851-2482A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279048 | ||||||
| chr6:131279100
|
A | G | 300 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.851-2430A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279100 | ||||||
| chr6:131279321
|
T | G | 8 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-2209T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279321 | ||||||
| chr6:131279546
|
C | T | 5 | a0001c0001t0005g0089a0001c0001t0005g0094a0001c0001t0007g0286others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-1984C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279546 | ||||||
| chr6:131280082
|
C | G | 10 | a0001c0001t0005g0089a0001c0001t0005g0094a0001c0001t0007g0286others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-1448C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280082 | ||||||
| chr6:131280206
|
T | C | 3 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-1324T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280206 | ||||||
| chr6:131280573
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-957C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280573 | ||||||
| chr6:131280650
|
C | T | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.851-880C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280650 | ||||||
| chr6:131280656
|
C | T | 3 | a0001c0001t0038g0166a0006c0006t0014g0003a0006c0006t0014g0004 | 3 | HG00741.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851-874C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280656 | ||||||
| chr6:131280685
|
C | T | 42 | a0001c0001t0004g0026a0001c0001t0004g0033a0001c0001t0004g0035others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280685 | ||||||
| chr6:131280697
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.851-833T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280697 | ||||||
| chr6:131280927
|
A | T | 16 | a0001c0001t0005g0092a0001c0001t0005g0140a0001c0001t0005g0156others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-603A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280927 | ||||||
| chr6:131280974
|
AT | A | 5 | a0001c0001t0041g0158a0002c0002t0017g0007a0002c0002t0017g0010others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-555delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280974 | ||||||
| chr6:131281073
|
G | C | 1 | a0002c0002t0020g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851-457G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281073 | ||||||
| chr6:131281396
|
A | G | 3 | a0001c0001t0038g0166a0006c0006t0014g0003a0006c0006t0014g0004 | 3 | HG00741.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851-134A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281396 | ||||||
| chr6:131281460
|
C | T | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.851-70C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281460 | ||||||
| chr6:131281462
|
G | T | 6 | a0001c0001t0005g0092a0001c0001t0005g0224a0001c0001t0007g0277others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-68G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281462 |