| geneid | 10142 |
|---|---|
| ensemblid | ENSG00000127914.19 |
| hgncid | 379 |
| symbol | AKAP9 |
| name | A-kinase anchoring protein 9 |
| refseq_nuc | NM_005751.5 |
| refseq_prot | NP_005742.4 |
| ensembl_nuc | ENST00000356239.8 |
| ensembl_prot | ENSP00000348573.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 91940862 |
| end | 92110673 |
| strand | + |
| ver | v1.2 |
| region | chr7:91940862-92110673 |
| region5000 | chr7:91935862-92115673 |
| regionname0 | AKAP9_chr7_91940862_92110673 |
| regionname5000 | AKAP9_chr7_91935862_92115673 |
| 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 | 0/0 | 3907 | 170 | 27 | 24 | 107 | 2 | 10 | 83 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002 | 0/0 | 3908 | 72 | 16 | 16 | 28 | 2 | 10 | 23 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0003 | 0/0 | 3908 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0004 | 0/0 | 3908 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0005 | 0/1 | 3907 | 9 | 0 | 2 | 3 | 0 | 3 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0006 | 0/0 | 3908 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0007 | 0/0 | 3908 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0008 | 0/0 | 3908 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0009 | 0/0 | 3908 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0010 | 0/0 | 3908 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0011 | 0/0 | 3908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0012 | 0/0 | 3908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0013 | 0/0 | 3908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0014 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0015 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0016 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0017 | 0/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0018 | 0/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0019 | 1/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0020 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0021 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0022 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0023 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0024 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0025 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0026 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0027 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0028 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| 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 | 0/0 | 11724 | 163 | 24 | 24 | 103 | 2 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0002 | 0/0 | 11727 | 71 | 16 | 15 | 28 | 2 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0003 | 0/0 | 11727 | 12 | 11 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0004 | 0/0 | 11727 | 10 | 8 | 2 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0005 | 0/1 | 11724 | 9 | 0 | 2 | 3 | 0 | 3 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0006 | 0/0 | 11727 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0007 | 0/0 | 11727 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0008 | 0/0 | 11724 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0009 | 0/0 | 11727 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0010 | 0/0 | 11727 | 2 | 0 | 0 | 1 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0011 | 0/0 | 11724 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0012 | 0/0 | 11727 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0013 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0014 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0015 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0016 | 1/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0017 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0018 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0019 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0020 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0021 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0022 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0023 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0024 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0025 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0026 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0027 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0028 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0029 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0030 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0031 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0032 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| c0033 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 753 | 206 | 43 | 30 | 114 | 2 | 16 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| t0002 | 1/0 | 753 | 97 | 39 | 18 | 28 | 1 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| t0003 | 0/0 | 756 | 3 | 0 | 2 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| 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 | 0/0 | 11724 | 163 | 24 | 24 | 103 | 2 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0008 | 0/0 | 11724 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0011 | 0/0 | 11724 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0018 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0022 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002c0002 | 0/0 | 11727 | 71 | 16 | 15 | 28 | 2 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002c0033 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0003c0003 | 0/0 | 11727 | 12 | 11 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0004c0004 | 0/0 | 11727 | 10 | 8 | 2 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0005c0005 | 0/1 | 11724 | 9 | 0 | 2 | 3 | 0 | 3 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0006c0006 | 0/0 | 11727 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0007c0007 | 0/0 | 11727 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0008c0009 | 0/0 | 11727 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0009c0012 | 0/0 | 11727 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0010c0010 | 0/0 | 11727 | 2 | 0 | 0 | 1 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0011c0029 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0012c0030 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0013c0031 | 0/0 | 11727 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0014c0013 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0015c0032 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0016c0028 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0017c0025 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0018c0023 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0019c0016 | 1/0 | 11724 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0020c0019 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0021c0020 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0022c0021 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0023c0024 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0024c0017 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0025c0026 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0026c0015 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0027c0027 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0028c0014 | 0/0 | 11727 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12476 | 163 | 24 | 24 | 103 | 2 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0008t0001 | 0/0 | 12476 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0011t0001 | 0/0 | 12476 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0018t0001 | 0/0 | 12476 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0001c0022t0001 | 0/0 | 12476 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002c0002t0002 | 0/0 | 12479 | 68 | 16 | 13 | 28 | 1 | 10 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002c0002t0003 | 0/0 | 12482 | 3 | 0 | 2 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0002c0033t0002 | 0/0 | 12479 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0003c0003t0002 | 0/0 | 12479 | 12 | 11 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0004c0004t0001 | 0/0 | 12479 | 10 | 8 | 2 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0005c0005t0001 | 0/1 | 12476 | 9 | 0 | 2 | 3 | 0 | 3 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0006c0006t0001 | 0/0 | 12479 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0007c0007t0002 | 0/0 | 12479 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0008c0009t0002 | 0/0 | 12479 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0009c0012t0002 | 0/0 | 12479 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0010c0010t0001 | 0/0 | 12479 | 2 | 0 | 0 | 1 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0011c0029t0002 | 0/0 | 12479 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0012c0030t0002 | 0/0 | 12479 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0013c0031t0002 | 0/0 | 12479 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0014c0013t0002 | 0/0 | 12479 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0015c0032t0002 | 0/0 | 12479 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0016c0028t0001 | 0/0 | 12476 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0017c0025t0001 | 0/0 | 12476 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0018c0023t0001 | 0/0 | 12476 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0019c0016t0002 | 1/0 | 12476 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0020c0019t0001 | 0/0 | 12476 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0021c0020t0001 | 0/0 | 12476 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0022c0021t0001 | 0/0 | 12476 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0023c0024t0001 | 0/0 | 12476 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0024c0017t0001 | 0/0 | 12476 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0025c0026t0001 | 0/0 | 12476 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0026c0015t0001 | 0/0 | 12479 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0027c0027t0001 | 0/0 | 12476 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| a0028c0014t0002 | 0/0 | 12479 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | copy fasta | chr7 | 91935862 | 92115673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0008t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0008t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0011t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0011t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0018t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0001c0022t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0002c0033t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0003c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0005c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0006c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0006c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0006c0006t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0006c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0007c0007t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0007c0007t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0007c0007t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0007c0007t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0008c0009t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0008c0009t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0008c0009t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0009c0012t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0009c0012t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0010c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0010c0010t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0011c0029t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0012c0030t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0013c0031t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0014c0013t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0015c0032t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0016c0028t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0017c0025t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0018c0023t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0019c0016t0002g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0020c0019t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0021c0020t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0022c0021t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0023c0024t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0024c0017t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0025c0026t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0026c0015t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0027c0027t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| a0028c0014t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0266 | EUR | FIN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00639 | hp1 | a0004 | c0004 | t0001 | g0206 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00642 | hp1 | a0011 | c0029 | t0002 | g0283 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00642 | hp2 | a0005 | c0005 | t0001 | g0128 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0268 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00735 | hp2 | a0024 | c0017 | t0001 | g0149 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00738 | hp1 | a0003 | c0003 | t0002 | g0290 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01070 | hp1 | a0002 | c0033 | t0002 | g0275 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0286 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01106 | hp1 | a0021 | c0020 | t0001 | g0141 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01168 | hp2 | a0002 | c0002 | t0003 | g0258 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01169 | hp1 | a0002 | c0002 | t0003 | g0261 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01169 | hp2 | a0005 | c0005 | t0001 | g0153 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0194 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0276 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01361 | hp1 | a0013 | c0031 | t0002 | g0278 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0285 | EUR | IBS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01884 | hp1 | a0006 | c0006 | t0001 | g0203 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0228 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0234 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01978 | hp1 | a0012 | c0030 | t0002 | g0229 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0227 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02129 | hp1 | a0005 | c0005 | t0001 | g0148 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | CDX | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02257 | hp1 | a0007 | c0007 | t0002 | g0287 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02258 | hp1 | a0003 | c0003 | t0002 | g0288 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02258 | hp2 | a0025 | c0026 | t0001 | g0075 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02280 | hp2 | a0008 | c0009 | t0002 | g0210 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0214 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02451 | hp2 | a0028 | c0014 | t0002 | g0208 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02523 | hp1 | a0022 | c0021 | t0001 | g0166 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02572 | hp1 | a0007 | c0007 | t0002 | g0304 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02572 | hp2 | a0003 | c0003 | t0002 | g0240 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02602 | hp2 | a0005 | c0005 | t0001 | g0147 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0215 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02630 | hp2 | a0007 | c0007 | t0002 | g0302 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0193 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02647 | hp2 | a0003 | c0003 | t0002 | g0212 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0292 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02717 | hp2 | a0020 | c0019 | t0001 | g0123 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02809 | hp1 | a0007 | c0007 | t0002 | g0303 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0202 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02818 | hp1 | a0006 | c0006 | t0001 | g0200 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0216 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02886 | hp1 | a0009 | c0012 | t0002 | g0217 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0306 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02895 | hp2 | a0003 | c0003 | t0002 | g0289 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02896 | hp2 | a0004 | c0004 | t0001 | g0205 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0305 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02922 | hp1 | a0001 | c0022 | t0001 | g0126 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02922 | hp2 | a0006 | c0006 | t0001 | g0198 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0197 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02976 | hp2 | a0008 | c0009 | t0002 | g0207 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03098 | hp1 | a0004 | c0004 | t0001 | g0196 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03139 | hp2 | a0006 | c0006 | t0001 | g0204 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0201 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03225 | hp2 | a0008 | c0009 | t0002 | g0209 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03239 | hp1 | a0005 | c0005 | t0001 | g0129 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0262 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0296 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0199 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0213 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0284 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03516 | hp2 | a0009 | c0012 | t0002 | g0218 | AFR | ESN | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03540 | hp2 | a0003 | c0003 | t0002 | g0301 | AFR | GWD | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03579 | hp1 | a0003 | c0003 | t0002 | g0294 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03688 | hp1 | a0010 | c0010 | t0001 | g0195 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0282 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0253 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0271 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04199 | hp1 | a0017 | c0025 | t0001 | g0063 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04204 | hp1 | a0018 | c0023 | t0001 | g0182 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0270 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18522 | hp1 | a0003 | c0003 | t0002 | g0295 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18522 | hp2 | a0003 | c0003 | t0002 | g0293 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | CHB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | CHB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18747 | hp1 | a0001 | c0008 | t0001 | g0091 | EAS | CHB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18747 | hp2 | a0005 | c0005 | t0001 | g0155 | EAS | CHB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18906 | hp1 | a0026 | c0015 | t0001 | g0001 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0250 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18939 | hp1 | a0016 | c0028 | t0001 | g0003 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18956 | hp1 | a0023 | c0024 | t0001 | g0160 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18974 | hp2 | a0001 | c0018 | t0001 | g0010 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19030 | hp1 | a0001 | c0011 | t0001 | g0013 | AFR | LWK | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | LWK | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19068 | hp1 | a0005 | c0005 | t0001 | g0154 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19074 | hp2 | a0001 | c0008 | t0001 | g0188 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19086 | hp1 | a0010 | c0010 | t0001 | g0191 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19087 | hp2 | a0001 | c0008 | t0001 | g0189 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19240 | hp1 | a0004 | c0004 | t0001 | g0192 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0252 | SAS | GIH | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA20905 | hp2 | a0005 | c0005 | t0001 | g0127 | SAS | GIH | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02109 | hp2 | a0003 | c0003 | t0002 | g0291 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02559 | hp1 | a0015 | c0032 | t0002 | g0239 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | ACB | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG03471 | hp2 | a0014 | c0013 | t0002 | g0211 | AFR | MSL | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0280 | AFR | USA | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| HG06807 | hp2 | a0027 | c0027 | t0001 | g0150 | AFR | USA | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0245 | AFR | USA | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA21309 | hp1 | a0001 | c0011 | t0001 | g0011 | AFR | LWK | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0297 | AFR | LWK | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0005 | t0001 | g0152 | REF | REF | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| homoSapiens_grch38 | hp1 | a0019 | c0016 | t0002 | g0272 | REF | REF | AKAP9_chr7_91935862_92115673 | AKAP9 | chr7 | 91935862 | 92115673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:92001218
|
G | A | 1 | a0006 | 4 | HG01884.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.1301G>A | p.Arg434Gln | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1539/12476 | 1301/11724 | 434/3907 | chr7 | 92001218 | ||
| chr7:92001289
|
G | C | 1 | a0028 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1372G>C | p.Ala458Pro | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1610/12476 | 1372/11724 | 458/3907 | chr7 | 92001289 | ||
| chr7:92001306
|
G | T | 11 | a0002a0003a0007others(8): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
missense_variant | MODERATE | c.1389G>T | p.Met463Ile | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1627/12476 | 1389/11724 | 463/3907 | chr7 | 92001306 | ||
| chr7:92001559
|
A | G | 1 | a0016 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1642A>G | p.Arg548Gly | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1880/12476 | 1642/11724 | 548/3907 | chr7 | 92001559 | ||
| chr7:92001568
|
A | G | 1 | a0015 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1651A>G | p.Ile551Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1889/12476 | 1651/11724 | 551/3907 | chr7 | 92001568 | ||
| chr7:92002342
|
A | G | 1 | a0027 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2425A>G | p.Ile809Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 2663/12476 | 2425/11724 | 809/3907 | chr7 | 92002342 | ||
| chr7:92017092
|
G | A | 1 | a0010 | 2 | HG03688.hp1 NA19086.hp1 |
missense_variant | MODERATE | c.3827G>A | p.Arg1276Gln | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/50 | 4065/12476 | 3827/11724 | 1276/3907 | chr7 | 92017092 | ||
| chr7:92022864
|
A | AAAC | 15 | a0002a0003a0004others(12): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
disruptive_inframe_insertion | MODERATE | c.4004_4006dupAAC | p.Lys1335_Leu1336ins others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/50 | 4245/12476 | 4007/11724 | 1336/3907 | INFO_REALIGN_3_PRIME | chr7 | 92022864 | |
| chr7:92029945
|
T | C | 3 | a0004a0006a0010 | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
missense_variant | MODERATE | c.4199T>C | p.Met1400Thr | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/50 | 4437/12476 | 4199/11724 | 1400/3907 | chr7 | 92029945 | ||
| chr7:92038599
|
G | C | 1 | a0014 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.4519G>C | p.Asp1507His | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/50 | 4757/12476 | 4519/11724 | 1507/3907 | chr7 | 92038599 | ||
| chr7:92040822
|
G | A | 1 | a0007 | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.4841G>A | p.Arg1614Gln | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/50 | 5079/12476 | 4841/11724 | 1614/3907 | chr7 | 92040822 | ||
| chr7:92052785
|
A | G | 1 | a0025 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.5428A>G | p.Met1810Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/50 | 5666/12476 | 5428/11724 | 1810/3907 | chr7 | 92052785 | ||
| chr7:92065387
|
A | G | 1 | a0009 | 2 | HG02886.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.6134A>G | p.Asn2045Ser | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 25/50 | 6372/12476 | 6134/11724 | 2045/3907 | chr7 | 92065387 | ||
| chr7:92079103
|
A | G | 1 | a0024 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.6970A>G | p.Ile2324Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/50 | 7208/12476 | 6970/11724 | 2324/3907 | chr7 | 92079103 | ||
| chr7:92079584
|
A | G | 2 | a0005a0024 | 10 | HG00642.hp2 HG00735.hp2 HG01169.hp2 others(7): Show |
missense_variant | MODERATE | c.7451A>G | p.Lys2484Arg | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/50 | 7689/12476 | 7451/11724 | 2484/3907 | chr7 | 92079584 | ||
| chr7:92079906
|
A | C | 1 | a0017 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.7773A>C | p.Gln2591His | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/50 | 8011/12476 | 7773/11724 | 2591/3907 | chr7 | 92079906 | ||
| chr7:92083198
|
A | G | 1 | a0023 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.8189A>G | p.Gln2730Arg | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/50 | 8427/12476 | 8189/11724 | 2730/3907 | chr7 | 92083198 | ||
| chr7:92083384
|
A | G | 4 | a0002a0011a0012others(1): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
missense_variant | MODERATE | c.8375A>G | p.Asn2792Ser | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/50 | 8613/12476 | 8375/11724 | 2792/3907 | chr7 | 92083384 | ||
| chr7:92085556
|
A | G | 1 | a0018 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.8894A>G | p.Tyr2965Cys | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 36/50 | 9132/12476 | 8894/11724 | 2965/3907 | chr7 | 92085556 | ||
| chr7:92085597
|
C | T | 27 | a0001a0002a0003others(24): Show | 305 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(302): Show |
missense_variant | MODERATE | c.8935C>T | p.Pro2979Ser | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 36/50 | 9173/12476 | 8935/11724 | 2979/3907 | chr7 | 92085597 | ||
| chr7:92096888
|
G | A | 1 | a0007 | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.9929G>A | p.Arg3310Gln | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 41/50 | 10167/12476 | 9929/11724 | 3310/3907 | chr7 | 92096888 | ||
| chr7:92097290
|
A | G | 2 | a0008a0026 | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.10331A>G | p.Gln3444Arg | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 41/50 | 10569/12476 | 10331/11724 | 3444/3907 | chr7 | 92097290 | ||
| chr7:92097734
|
G | A | 1 | a0011 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.10547G>A | p.Arg3516Lys | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/50 | 10785/12476 | 10547/11724 | 3516/3907 | chr7 | 92097734 | ||
| chr7:92099813
|
A | G | 1 | a0013 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.10840A>G | p.Met3614Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/50 | 11078/12476 | 10840/11724 | 3614/3907 | chr7 | 92099813 | ||
| chr7:92099831
|
A | G | 1 | a0009 | 2 | HG02886.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.10858A>G | p.Ile3620Val | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/50 | 11096/12476 | 10858/11724 | 3620/3907 | chr7 | 92099831 | ||
| chr7:92102730
|
G | A | 1 | a0020 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.11234G>A | p.Gly3745Glu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/50 | 11472/12476 | 11234/11724 | 3745/3907 | chr7 | 92102730 | ||
| chr7:92102769
|
G | A | 1 | a0021 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.11273G>A | p.Arg3758His | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/50 | 11511/12476 | 11273/11724 | 3758/3907 | chr7 | 92102769 | ||
| chr7:92108520
|
A | G | 1 | a0012 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.11573A>G | p.Asn3858Ser | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/50 | 11811/12476 | 11573/11724 | 3858/3907 | chr7 | 92108520 | ||
| chr7:92110149
|
T | C | 1 | a0022 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.11714T>C | p.Met3905Thr | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 50/50 | 11952/12476 | 11714/11724 | 3905/3907 | chr7 | 92110149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:91973743
|
G | A | 1 | a0014c0013 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.81G>A | p.Ser27Ser | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/50 | 319/12476 | 81/11724 | 27/3907 | chr7 | 91973743 | ||
| chr7:91995617
|
A | G | 1 | a0007c0007 | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.747A>G | p.Glu249Glu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/50 | 985/12476 | 747/11724 | 249/3907 | chr7 | 91995617 | ||
| chr7:92001453
|
C | T | 1 | a0002c0033 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.1536C>T | p.Leu512Leu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 1774/12476 | 1536/11724 | 512/3907 | chr7 | 92001453 | ||
| chr7:92002699
|
T | C | 2 | a0008c0009a0026c0015 | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.2782T>C | p.Leu928Leu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 3020/12476 | 2782/11724 | 928/3907 | chr7 | 92002699 | ||
| chr7:92002992
|
C | T | 30 | a0001c0001a0001c0008a0001c0011others(27): Show | 295 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(292): Show |
synonymous_variant | LOW | c.3075C>T | p.Thr1025Thr | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/50 | 3313/12476 | 3075/11724 | 1025/3907 | chr7 | 92002992 | ||
| chr7:92012614
|
A | G | 13 | a0002c0002a0002c0033a0003c0003others(10): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
synonymous_variant | LOW | c.3504A>G | p.Glu1168Glu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/50 | 3742/12476 | 3504/11724 | 1168/3907 | chr7 | 92012614 | ||
| chr7:92062287
|
C | T | 12 | a0002c0002a0002c0033a0003c0003others(9): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
synonymous_variant | LOW | c.5778C>T | p.Gly1926Gly | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/50 | 6016/12476 | 5778/11724 | 1926/3907 | chr7 | 92062287 | ||
| chr7:92084658
|
C | T | 13 | a0002c0002a0002c0033a0003c0003others(10): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
synonymous_variant | LOW | c.8665C>T | p.Leu2889Leu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 34/50 | 8903/12476 | 8665/11724 | 2889/3907 | chr7 | 92084658 | ||
| chr7:92086348
|
C | T | 5 | a0002c0002a0002c0033a0011c0029others(2): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
synonymous_variant | LOW | c.9145C>T | p.Leu3049Leu | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/50 | 9383/12476 | 9145/11724 | 3049/3907 | chr7 | 92086348 | ||
| chr7:92095092
|
A | G | 1 | a0001c0011 | 2 | NA19030.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.9648A>G | p.Lys3216Lys | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/50 | 9886/12476 | 9648/11724 | 3216/3907 | chr7 | 92095092 | ||
| chr7:92097613
|
A | C | 14 | a0001c0022a0002c0002a0002c0033others(11): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
synonymous_variant | LOW | c.10426A>C | p.Arg3476Arg | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/50 | 10664/12476 | 10426/11724 | 3476/3907 | chr7 | 92097613 | ||
| chr7:92099818
|
G | A | 1 | a0001c0008 | 3 | NA18747.hp1 NA19074.hp2 NA19087.hp2 |
synonymous_variant | LOW | c.10845G>A | p.Lys3615Lys | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/50 | 11083/12476 | 10845/11724 | 3615/3907 | chr7 | 92099818 | ||
| chr7:92100885
|
C | A | 1 | a0001c0018 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.10926C>A | p.Ala3642Ala | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/50 | 11164/12476 | 10926/11724 | 3642/3907 | chr7 | 92100885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:91940883
|
T | TGGC | 1 | a0002c0002t0003 | 3 | HG00280.hp2 HG01168.hp2 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-202_-200dupCGG | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/50 | 199 | INFO_REALIGN_3_PRIME | chr7 | 91940883 | ||||
| chr7:91940976
|
G | C | 20 | a0001c0001t0001a0001c0008t0001a0001c0011t0001others(17): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/50 | 124 | chr7 | 91940976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:91941198
|
C | T | 2 | a0002c0002t0002g0305a0002c0002t0002g0306 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.48+51C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941198 | ||||||
| chr7:91941301
|
C | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.48+154C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941301 | ||||||
| chr7:91941476
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.48+329T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941476 | ||||||
| chr7:91941760
|
A | G | 112 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.48+613A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941760 | ||||||
| chr7:91941882
|
T | TTG | 21 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(18): Show | 21 | HG00738.hp1 HG01109.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.48+764_48+765dupTG | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91941882 | |||||
| chr7:91941882
|
T | TTGTG | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 72 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.48+762_48+765dupTG others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91941882 | |||||
| chr7:91941882
|
T | TTGTGTG | 18 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00597.hp2 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.48+760_48+765dupTG others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91941882 | |||||
| chr7:91941882
|
T | TTGTGTGT others(1): Show |
83 | a0001c0001t0001g0078a0001c0001t0001g0094a0001c0001t0001g0095others(80): Show | 83 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.48+758_48+765dupTG others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91941882 | |||||
| chr7:91941882
|
T | TTGTGTGT others(3): Show |
27 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(24): Show | 27 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.48+756_48+765dupTG others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91941882 | |||||
| chr7:91941913
|
A | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+766A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941913 | ||||||
| chr7:91941914
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+767A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941914 | ||||||
| chr7:91941977
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48+830T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91941977 | ||||||
| chr7:91942073
|
C | G | 1 | a0003c0003t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.48+926C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91942073 | ||||||
| chr7:91942165
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.48+1018T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91942165 | ||||||
| chr7:91942231
|
G | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.48+1084G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91942231 | ||||||
| chr7:91942359
|
A | G | 19 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0157others(16): Show | 19 | HG00597.hp1 HG02523.hp1 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.48+1212A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91942359 | ||||||
| chr7:91943034
|
T | TA | 49 | a0001c0001t0001g0006a0001c0001t0001g0080a0001c0001t0001g0085others(46): Show | 49 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.48+1899dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91943034 | |||||
| chr7:91943252
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0187 | 2 | NA18955.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.48+2105G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943252 | ||||||
| chr7:91943430
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+2283A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943430 | ||||||
| chr7:91943435
|
T | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 256 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.48+2288T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943435 | ||||||
| chr7:91943437
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+2290T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943437 | ||||||
| chr7:91943548
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.48+2401A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943548 | ||||||
| chr7:91943579
|
G | A | 1 | a0020c0019t0001g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.48+2432G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943579 | ||||||
| chr7:91943768
|
C | T | 1 | a0002c0002t0002g0241 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.48+2621C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943768 | ||||||
| chr7:91943994
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.48+2847G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91943994 | ||||||
| chr7:91944152
|
A | G | 112 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.48+3005A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944152 | ||||||
| chr7:91944280
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+3133G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944280 | ||||||
| chr7:91944398
|
A | AT | 6 | a0001c0001t0001g0064a0001c0001t0001g0077a0001c0001t0001g0122others(3): Show | 6 | HG02074.hp2 HG02723.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+3265dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91944398 | |||||
| chr7:91944435
|
G | A | 265 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.48+3288G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944435 | ||||||
| chr7:91944474
|
C | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.48+3327C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944474 | ||||||
| chr7:91944617
|
C | T | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.48+3470C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944617 | ||||||
| chr7:91944796
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.48+3649T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944796 | ||||||
| chr7:91944814
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+3667G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944814 | ||||||
| chr7:91944952
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.48+3805G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91944952 | ||||||
| chr7:91945134
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.48+3987G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91945134 | ||||||
| chr7:91945203
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.48+4056A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91945203 | ||||||
| chr7:91945904
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+4757A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91945904 | ||||||
| chr7:91946048
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+4901A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946048 | ||||||
| chr7:91946073
|
C | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48+4926C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946073 | ||||||
| chr7:91946103
|
C | T | 112 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.48+4956C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946103 | ||||||
| chr7:91946284
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.48+5137G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946284 | ||||||
| chr7:91946308
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48+5161T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946308 | ||||||
| chr7:91946377
|
T | C | 1 | a0003c0003t0002g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.48+5230T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946377 | ||||||
| chr7:91946383
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+5236A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946383 | ||||||
| chr7:91946395
|
C | CT | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(220): Show | 223 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.48+5261dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91946395 | |||||
| chr7:91946474
|
T | C | 1 | a0018c0023t0001g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.48+5327T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946474 | ||||||
| chr7:91946708
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18940.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.48+5561T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946708 | ||||||
| chr7:91946901
|
A | G | 1 | a0003c0003t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.48+5754A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91946901 | ||||||
| chr7:91947157
|
GGT | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+6026_48+6027del others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91947157 | |||||
| chr7:91947159
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02056.hp2 HG03486.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+6012T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947159 | ||||||
| chr7:91947175
|
CGT | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+6048_48+6049del others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91947175 | |||||
| chr7:91947210
|
G | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18942.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.48+6063G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947210 | ||||||
| chr7:91947481
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.48+6334T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947481 | ||||||
| chr7:91947510
|
G | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(232): Show | 235 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.48+6363G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947510 | ||||||
| chr7:91947630
|
G | A | 2 | a0010c0010t0001g0191a0010c0010t0001g0195 | 2 | HG03688.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.48+6483G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947630 | ||||||
| chr7:91947644
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+6497A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947644 | ||||||
| chr7:91947931
|
T | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.48+6784T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91947931 | ||||||
| chr7:91948092
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+6945G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91948092 | ||||||
| chr7:91948605
|
CT | C | 76 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(73): Show | 76 | HG00280.hp2 HG00639.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.48+7481delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91948605 | |||||
| chr7:91948605
|
CTTTTTTT others(2): Show |
C | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.48+7473_48+7481del others(9): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91948605 | |||||
| chr7:91948605
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0098a0001c0018t0001g0010 | 2 | NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.48+7472_48+7481del others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91948605 | |||||
| chr7:91948800
|
GATGGGGT others(130): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+7659_48+7795del | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91948800 | |||||
| chr7:91948814
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+7667A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91948814 | ||||||
| chr7:91948861
|
G | A | 1 | a0002c0002t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+7714G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91948861 | ||||||
| chr7:91949133
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.48+7986T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91949133 | ||||||
| chr7:91949158
|
AAT | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0058others(4): Show | 7 | HG00423.hp1 NA18945.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+8022_48+8023del others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91949158 | |||||
| chr7:91949325
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.48+8178G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91949325 | ||||||
| chr7:91949429
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48+8282G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91949429 | ||||||
| chr7:91949759
|
A | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+8612A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91949759 | ||||||
| chr7:91950224
|
T | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.48+9077T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950224 | ||||||
| chr7:91950227
|
C | CT | 8 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0076others(5): Show | 8 | HG02572.hp2 HG03453.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+9100dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91950227 | |||||
| chr7:91950299
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48+9152G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950299 | ||||||
| chr7:91950402
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.48+9255C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950402 | ||||||
| chr7:91950466
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+9319A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950466 | ||||||
| chr7:91950538
|
C | T | 2 | a0005c0005t0001g0154a0005c0005t0001g0155 | 2 | NA18747.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.48+9391C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950538 | ||||||
| chr7:91950550
|
A | C | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.48+9403A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950550 | ||||||
| chr7:91950668
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48+9521G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950668 | ||||||
| chr7:91950716
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.48+9569G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950716 | ||||||
| chr7:91950858
|
A | G | 2 | a0005c0005t0001g0152a0005c0005t0001g0153 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.48+9711A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950858 | ||||||
| chr7:91950953
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | NA18952.hp2 NA18953.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.48+9806A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950953 | ||||||
| chr7:91950973
|
A | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.48+9826A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950973 | ||||||
| chr7:91950981
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.48+9834A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91950981 | ||||||
| chr7:91951022
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+9875G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951022 | ||||||
| chr7:91951023
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+9876A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951023 | ||||||
| chr7:91951102
|
T | C | 1 | a0002c0002t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.48+9955T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951102 | ||||||
| chr7:91951176
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.48+10029A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951176 | ||||||
| chr7:91951257
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.48+10110A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951257 | ||||||
| chr7:91951340
|
T | C | 2 | a0002c0002t0002g0252a0002c0002t0002g0253 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.48+10193T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951340 | ||||||
| chr7:91951807
|
C | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.48+10660C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951807 | ||||||
| chr7:91951836
|
C | G | 11 | a0003c0003t0002g0212a0003c0003t0002g0288a0003c0003t0002g0289others(8): Show | 11 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+10689C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91951836 | ||||||
| chr7:91951856
|
CAG | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 10 | HG00738.hp2 HG01256.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+10712_48+10713d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91951856 | |||||
| chr7:91952189
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.48+11042C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952189 | ||||||
| chr7:91952252
|
T | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+11105T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952252 | ||||||
| chr7:91952268
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.48+11121T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952268 | ||||||
| chr7:91952403
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+11256A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952403 | ||||||
| chr7:91952869
|
C | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+11722C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952869 | ||||||
| chr7:91952881
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.48+11734G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952881 | ||||||
| chr7:91952891
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+11744G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91952891 | ||||||
| chr7:91953511
|
A | G | 1 | a0002c0002t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+12364A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953511 | ||||||
| chr7:91953542
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.48+12395G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953542 | ||||||
| chr7:91953625
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48+12478A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953625 | ||||||
| chr7:91953812
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.48+12665G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953812 | ||||||
| chr7:91953813
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.48+12666C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953813 | ||||||
| chr7:91953818
|
CA | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 171 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.48+12672delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953818 | ||||||
| chr7:91953819
|
A | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(39): Show | 42 | HG00280.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+12672A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91953819 | ||||||
| chr7:91954020
|
C | T | 113 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0001g0080others(110): Show | 113 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.48+12873C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91954020 | ||||||
| chr7:91954458
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+13311T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91954458 | ||||||
| chr7:91954532
|
T | G | 1 | a0017c0025t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.48+13385T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91954532 | ||||||
| chr7:91954710
|
A | AT | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.48+13569dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91954710 | |||||
| chr7:91954901
|
A | G | 2 | a0002c0002t0002g0267a0002c0002t0002g0268 | 2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.48+13754A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91954901 | ||||||
| chr7:91954967
|
A | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.48+13820A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91954967 | ||||||
| chr7:91955040
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0167a0001c0001t0001g0187others(1): Show | 4 | HG00597.hp1 NA18955.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+13893A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955040 | ||||||
| chr7:91955041
|
C | T | 1 | a0007c0007t0002g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.48+13894C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955041 | ||||||
| chr7:91955042
|
A | G | 111 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(108): Show | 111 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.48+13895A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955042 | ||||||
| chr7:91955570
|
T | C | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48+14423T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955570 | ||||||
| chr7:91955572
|
T | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA19066.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.48+14425T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955572 | ||||||
| chr7:91955602
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.48+14455A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955602 | ||||||
| chr7:91955638
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+14491A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955638 | ||||||
| chr7:91955727
|
G | A | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+14580G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955727 | ||||||
| chr7:91955831
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+14684G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955831 | ||||||
| chr7:91955834
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.48+14687G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955834 | ||||||
| chr7:91955876
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.48+14729G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955876 | ||||||
| chr7:91955926
|
C | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.48+14779C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955926 | ||||||
| chr7:91955944
|
T | A | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.48+14797T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955944 | ||||||
| chr7:91955949
|
T | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.48+14802T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91955949 | ||||||
| chr7:91956139
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(8): Show | 11 | HG01081.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+14992G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956139 | ||||||
| chr7:91956171
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48+15024C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956171 | ||||||
| chr7:91956183
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48+15036G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956183 | ||||||
| chr7:91956316
|
C | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.48+15169C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956316 | ||||||
| chr7:91956368
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.48+15221C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956368 | ||||||
| chr7:91956379
|
AAC | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0077 | 3 | HG02486.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.48+15234_48+15235d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91956379 | |||||
| chr7:91956392
|
T | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+15245T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956392 | ||||||
| chr7:91956399
|
CA | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.48+15273delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91956399 | |||||
| chr7:91956399
|
CAAAAAA | C | 93 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.48+15268_48+15273d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91956399 | |||||
| chr7:91956621
|
A | G | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.48+15474A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956621 | ||||||
| chr7:91956912
|
G | A | 1 | a0001c0011t0001g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.48+15765G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91956912 | ||||||
| chr7:91957075
|
A | G | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.48+15928A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91957075 | ||||||
| chr7:91957265
|
TTAAATAA others(4): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.48+16119_48+16129d others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91957265 | ||||||
| chr7:91957510
|
G | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-16201G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91957510 | ||||||
| chr7:91957681
|
A | G | 1 | a0004c0004t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-16030A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91957681 | ||||||
| chr7:91957736
|
T | G | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-15975T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91957736 | ||||||
| chr7:91958163
|
G | C | 94 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(91): Show | 94 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.49-15548G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958163 | ||||||
| chr7:91958225
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-15486T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958225 | ||||||
| chr7:91958455
|
C | T | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.49-15256C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958455 | ||||||
| chr7:91958464
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49-15247C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958464 | ||||||
| chr7:91958512
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-15199G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958512 | ||||||
| chr7:91958642
|
C | T | 1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.49-15069C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958642 | ||||||
| chr7:91958722
|
G | A | 94 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(91): Show | 94 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.49-14989G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958722 | ||||||
| chr7:91958801
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.49-14910A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958801 | ||||||
| chr7:91958858
|
AT | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-14843delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91958858 | |||||
| chr7:91958877
|
C | CATT | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 60 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-14812_49-14810d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91958877 | |||||
| chr7:91958880
|
T | C | 95 | a0001c0001t0001g0064a0002c0002t0002g0213a0002c0002t0002g0214others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-14831T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958880 | ||||||
| chr7:91958883
|
T | C | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49-14828T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958883 | ||||||
| chr7:91958975
|
C | G | 1 | a0002c0002t0003g0266 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49-14736C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91958975 | ||||||
| chr7:91959046
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-14665G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959046 | ||||||
| chr7:91959328
|
T | C | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-14383T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959328 | ||||||
| chr7:91959331
|
C | T | 1 | a0002c0002t0002g0236 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.49-14380C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959331 | ||||||
| chr7:91959350
|
G | A | 100 | a0001c0001t0001g0172a0002c0002t0002g0213a0002c0002t0002g0214others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.49-14361G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959350 | ||||||
| chr7:91959459
|
AT | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-14249delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91959459 | |||||
| chr7:91959462
|
T | TA | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-14234dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91959462 | |||||
| chr7:91959462
|
TA | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(78): Show | 81 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.49-14234delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91959462 | |||||
| chr7:91959462
|
TAA | T | 93 | a0001c0001t0001g0164a0002c0002t0002g0213a0002c0002t0002g0214others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.49-14235_49-14234d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91959462 | |||||
| chr7:91959644
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.49-14067A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959644 | ||||||
| chr7:91959726
|
T | TAAAAAAA others(324): Show |
1 | a0002c0002t0002g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.49-13973_49-13972i others(333): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91959726 | |||||
| chr7:91959814
|
T | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-13897T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91959814 | ||||||
| chr7:91960044
|
G | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0184others(1): Show | 4 | HG03831.hp1 HG04204.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-13667G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91960044 | ||||||
| chr7:91961094
|
A | G | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-12617A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961094 | ||||||
| chr7:91961097
|
A | G | 2 | a0003c0003t0002g0212a0028c0014t0002g0208 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.49-12614A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961097 | ||||||
| chr7:91961182
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.49-12529C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961182 | ||||||
| chr7:91961185
|
A | C | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49-12526A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961185 | ||||||
| chr7:91961253
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.49-12458G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961253 | ||||||
| chr7:91961332
|
G | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-12379G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961332 | ||||||
| chr7:91961500
|
G | A | 3 | a0002c0002t0002g0273a0002c0002t0002g0274a0002c0002t0002g0276 | 3 | HG01256.hp1 HG01261.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.49-12211G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91961500 | ||||||
| chr7:91962134
|
A | G | 5 | a0002c0002t0002g0251a0002c0002t0002g0264a0002c0002t0002g0265others(2): Show | 5 | HG02155.hp1 NA18612.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-11577A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91962134 | ||||||
| chr7:91962389
|
T | A | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49-11322T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91962389 | ||||||
| chr7:91962474
|
T | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-11237T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91962474 | ||||||
| chr7:91962575
|
G | A | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49-11136G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91962575 | ||||||
| chr7:91962795
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-10916C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91962795 | ||||||
| chr7:91962836
|
CTG | C | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-10873_49-10872d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91962836 | |||||
| chr7:91963048
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49-10663A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963048 | ||||||
| chr7:91963088
|
ATCTTT | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-10616_49-10612d others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963088 | |||||
| chr7:91963158
|
A | G | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.49-10553A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963158 | ||||||
| chr7:91963183
|
T | A | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.49-10528T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963183 | ||||||
| chr7:91963441
|
T | C | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-10270T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963441 | ||||||
| chr7:91963481
|
G | GTC | 7 | a0002c0002t0002g0249a0002c0002t0002g0251a0002c0002t0002g0268others(4): Show | 7 | HG00639.hp2 HG00735.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10229_49-10228d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963481 | |||||
| chr7:91963482
|
T | TCA | 34 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0080others(31): Show | 34 | HG00423.hp2 HG00621.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.49-10184_49-10183d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCACA | 43 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-10186_49-10183d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCACACA | 20 | a0001c0001t0001g0019a0001c0001t0001g0079a0001c0001t0001g0102others(17): Show | 20 | HG00597.hp1 HG01081.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.49-10188_49-10183d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCACACAC others(1): Show |
10 | a0001c0001t0001g0101a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG00738.hp2 HG02071.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-10190_49-10183d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0181a0002c0002t0002g0238 | 3 | HG02074.hp2 NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.49-10192_49-10183d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0156 | 2 | NA18951.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.49-10194_49-10183d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCTCA | 12 | a0002c0002t0002g0242a0002c0002t0002g0246a0002c0002t0002g0247others(9): Show | 12 | HG00642.hp1 HG01192.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.49-10228_49-10227i others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCTCACA | 14 | a0002c0002t0002g0243a0002c0002t0002g0244a0002c0002t0002g0245others(11): Show | 14 | HG00280.hp2 HG01109.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-10228_49-10227i others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCTCACAC others(1): Show |
13 | a0001c0001t0001g0163a0001c0001t0001g0165a0002c0002t0002g0255others(10): Show | 13 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.49-10228_49-10227i others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCTCACAC others(3): Show |
2 | a0002c0002t0002g0254a0002c0002t0002g0300 | 2 | NA18979.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.49-10228_49-10227i others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
T | TCTCACAC others(5): Show |
1 | a0002c0002t0002g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49-10228_49-10227i others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCA | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01169.hp2 HG01516.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-10184_49-10183d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACA | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.49-10186_49-10183d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACA | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(40): Show | 43 | HG00423.hp1 HG00621.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.49-10188_49-10183d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(1): Show |
T | 12 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0049others(9): Show | 12 | HG00639.hp1 HG01109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-10190_49-10183d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(3): Show |
T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49-10192_49-10183d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(5): Show |
T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49-10194_49-10183d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(9): Show |
T | 1 | a0004c0004t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49-10198_49-10183d others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(11): Show |
T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-10200_49-10183d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963482
|
TCACACAC others(13): Show |
T | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49-10202_49-10183d others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91963482 | |||||
| chr7:91963484
|
A | T | 9 | a0002c0002t0002g0250a0002c0002t0002g0253a0002c0002t0002g0274others(6): Show | 9 | HG01256.hp1 HG01261.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.49-10227A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963484 | ||||||
| chr7:91963486
|
A | T | 1 | a0008c0009t0002g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49-10225A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963486 | ||||||
| chr7:91963488
|
A | T | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-10223A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963488 | ||||||
| chr7:91963490
|
A | T | 1 | a0003c0003t0002g0295 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49-10221A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963490 | ||||||
| chr7:91963492
|
A | T | 2 | a0003c0003t0002g0212a0028c0014t0002g0208 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.49-10219A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963492 | ||||||
| chr7:91963494
|
A | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49-10217A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963494 | ||||||
| chr7:91963496
|
A | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49-10215A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963496 | ||||||
| chr7:91963529
|
T | C | 1 | a0002c0002t0002g0277 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.49-10182T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963529 | ||||||
| chr7:91963532
|
T | A | 1 | a0002c0002t0002g0277 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.49-10179T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963532 | ||||||
| chr7:91963604
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-10107G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963604 | ||||||
| chr7:91963704
|
G | A | 1 | a0002c0002t0002g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.49-10007G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963704 | ||||||
| chr7:91963761
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-9950G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963761 | ||||||
| chr7:91963761
|
G | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.49-9950G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91963761 | ||||||
| chr7:91964914
|
T | A | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.49-8797T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91964914 | ||||||
| chr7:91964967
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-8744A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91964967 | ||||||
| chr7:91964972
|
GT | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-8738delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91964972 | ||||||
| chr7:91964986
|
A | C | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49-8725A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91964986 | ||||||
| chr7:91965196
|
T | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-8515T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965196 | ||||||
| chr7:91965281
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.49-8430T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965281 | ||||||
| chr7:91965423
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49-8288C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965423 | ||||||
| chr7:91965803
|
G | T | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-7908G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965803 | ||||||
| chr7:91965824
|
T | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-7887T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965824 | ||||||
| chr7:91965994
|
A | G | 4 | a0002c0002t0002g0267a0002c0002t0002g0268a0002c0002t0002g0305others(1): Show | 4 | HG00735.hp1 HG01192.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-7717A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91965994 | ||||||
| chr7:91966282
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.49-7429A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91966282 | ||||||
| chr7:91966661
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.49-7050A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91966661 | ||||||
| chr7:91966807
|
G | C | 94 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(91): Show | 94 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.49-6904G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91966807 | ||||||
| chr7:91967364
|
G | A | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.49-6347G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967364 | ||||||
| chr7:91967492
|
T | A | 1 | a0011c0029t0002g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.49-6219T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967492 | ||||||
| chr7:91967651
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-6060C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967651 | ||||||
| chr7:91967700
|
G | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-6011G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967700 | ||||||
| chr7:91967836
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-5875C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967836 | ||||||
| chr7:91967876
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.49-5835T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967876 | ||||||
| chr7:91967953
|
C | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-5758C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91967953 | ||||||
| chr7:91968255
|
T | C | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.49-5456T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968255 | ||||||
| chr7:91968606
|
G | T | 6 | a0002c0002t0002g0221a0002c0002t0002g0224a0002c0002t0002g0225others(3): Show | 6 | NA18991.hp2 NA18992.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-5105G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968606 | ||||||
| chr7:91968620
|
C | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-5091C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968620 | ||||||
| chr7:91968640
|
G | A | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.49-5071G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968640 | ||||||
| chr7:91968679
|
G | A | 2 | a0001c0001t0001g0047a0026c0015t0001g0001 | 2 | HG01361.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.49-5032G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968679 | ||||||
| chr7:91968732
|
T | C | 13 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(10): Show | 13 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.49-4979T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968732 | ||||||
| chr7:91968802
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.49-4909C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968802 | ||||||
| chr7:91968850
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.49-4861C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91968850 | ||||||
| chr7:91969129
|
T | A | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-4582T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969129 | ||||||
| chr7:91969170
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.49-4541A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969170 | ||||||
| chr7:91969431
|
C | T | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-4280C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969431 | ||||||
| chr7:91969503
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-4208G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969503 | ||||||
| chr7:91969513
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-4198T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969513 | ||||||
| chr7:91969564
|
C | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.49-4147C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969564 | ||||||
| chr7:91969715
|
G | A | 1 | a0004c0004t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49-3996G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969715 | ||||||
| chr7:91969729
|
G | A | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49-3982G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969729 | ||||||
| chr7:91969792
|
G | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.49-3919G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91969792 | ||||||
| chr7:91970399
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.49-3312C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970399 | ||||||
| chr7:91970459
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.49-3252T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970459 | ||||||
| chr7:91970511
|
A | C | 98 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(95): Show | 98 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.49-3200A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970511 | ||||||
| chr7:91970511
|
A | G | 1 | a0002c0002t0002g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.49-3200A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970511 | ||||||
| chr7:91970543
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.49-3168T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970543 | ||||||
| chr7:91970863
|
G | A | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49-2848G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970863 | ||||||
| chr7:91970869
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49-2842A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91970869 | ||||||
| chr7:91971092
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.49-2619A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971092 | ||||||
| chr7:91971162
|
C | A | 1 | a0005c0005t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.49-2549C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971162 | ||||||
| chr7:91971334
|
C | A | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.49-2377C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971334 | ||||||
| chr7:91971491
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.49-2220G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971491 | ||||||
| chr7:91971499
|
T | G | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-2212T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971499 | ||||||
| chr7:91971560
|
C | CT | 98 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0047others(95): Show | 98 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.49-2126dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971560 | |||||
| chr7:91971560
|
C | CTT | 10 | a0001c0001t0001g0002a0001c0001t0001g0089a0002c0002t0002g0213others(7): Show | 10 | HG00735.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-2127_49-2126dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971560 | |||||
| chr7:91971560
|
CT | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0110others(5): Show | 8 | NA18951.hp1 NA18956.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-2126delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971560 | |||||
| chr7:91971629
|
G | A | 2 | a0002c0002t0002g0264a0002c0002t0002g0269 | 2 | NA18612.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.49-2082G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971629 | ||||||
| chr7:91971696
|
T | G | 1 | a0002c0002t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.49-2015T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971696 | ||||||
| chr7:91971964
|
CTT | C | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-1744_49-1743del others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971964 | |||||
| chr7:91971980
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-1731C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971980 | ||||||
| chr7:91971981
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-1730T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971981 | ||||||
| chr7:91971982
|
C | CT | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.49-1709dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971982 | |||||
| chr7:91971982
|
C | CTT | 22 | a0002c0002t0002g0252a0002c0002t0002g0253a0002c0002t0002g0254others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-1710_49-1709dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971982 | |||||
| chr7:91971982
|
C | CTTT | 59 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(56): Show | 59 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.49-1711_49-1709dup others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971982 | |||||
| chr7:91971982
|
C | CTTTT | 12 | a0002c0002t0002g0221a0002c0002t0002g0241a0002c0002t0002g0242others(9): Show | 12 | HG00639.hp2 HG02071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.49-1712_49-1709dup others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91971982 | |||||
| chr7:91971982
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-1729C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91971982 | ||||||
| chr7:91972089
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-1622A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972089 | ||||||
| chr7:91972151
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-1560G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972151 | ||||||
| chr7:91972204
|
C | G | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49-1507C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972204 | ||||||
| chr7:91972219
|
G | A | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49-1492G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972219 | ||||||
| chr7:91972230
|
C | T | 13 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(10): Show | 13 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.49-1481C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972230 | ||||||
| chr7:91972259
|
T | A | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-1452T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972259 | ||||||
| chr7:91972260
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-1451A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972260 | ||||||
| chr7:91972292
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.49-1419C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972292 | ||||||
| chr7:91972295
|
G | A | 1 | a0005c0005t0001g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.49-1416G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972295 | ||||||
| chr7:91972349
|
G | C | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.49-1362G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972349 | ||||||
| chr7:91972442
|
G | T | 1 | a0002c0002t0002g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49-1269G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972442 | ||||||
| chr7:91972616
|
A | G | 83 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(80): Show | 83 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.49-1095A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972616 | ||||||
| chr7:91972664
|
A | G | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.49-1047A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972664 | ||||||
| chr7:91972713
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49-998A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972713 | ||||||
| chr7:91972719
|
G | GTTTTTTG others(8): Show |
1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.49-987_49-986insTG others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | INFO_REALIGN_3_PRIME | chr7 | 91972719 | |||||
| chr7:91972737
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49-974T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972737 | ||||||
| chr7:91972905
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.49-806C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91972905 | ||||||
| chr7:91973071
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0114others(1): Show | 4 | HG00423.hp2 NA18945.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-640A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91973071 | ||||||
| chr7:91973152
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 303 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.49-559A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91973152 | ||||||
| chr7:91973302
|
G | A | 2 | a0004c0004t0001g0197a0004c0004t0001g0201 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.49-409G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91973302 | ||||||
| chr7:91973331
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.49-380C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91973331 | ||||||
| chr7:91973690
|
G | A | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-21G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 1/49 | chr7 | 91973690 | ||||||
| chr7:91974031
|
T | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+63T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974031 | ||||||
| chr7:91974123
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.306+155T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974123 | ||||||
| chr7:91974142
|
G | C | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.306+174G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974142 | ||||||
| chr7:91974306
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.306+338A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974306 | ||||||
| chr7:91974319
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.306+351G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974319 | ||||||
| chr7:91974332
|
A | AT | 98 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(95): Show | 98 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.306+372dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91974332 | |||||
| chr7:91974570
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+602A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974570 | ||||||
| chr7:91974885
|
C | CT | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+918dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91974885 | |||||
| chr7:91974913
|
T | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.306+945T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91974913 | ||||||
| chr7:91975006
|
A | T | 6 | a0002c0002t0002g0221a0002c0002t0002g0224a0002c0002t0002g0225others(3): Show | 6 | NA18991.hp2 NA18992.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+1038A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975006 | ||||||
| chr7:91975142
|
G | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.306+1174G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975142 | ||||||
| chr7:91975751
|
A | G | 1 | a0002c0033t0002g0275 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.306+1783A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975751 | ||||||
| chr7:91975809
|
A | G | 1 | a0003c0003t0002g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.306+1841A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975809 | ||||||
| chr7:91975867
|
G | T | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.306+1899G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975867 | ||||||
| chr7:91975912
|
TG | T | 111 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(108): Show | 111 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.306+1945delG | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975912 | ||||||
| chr7:91975913
|
G | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1945G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975913 | ||||||
| chr7:91975917
|
G | T | 1 | a0004c0004t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.306+1949G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975917 | ||||||
| chr7:91975923
|
TTG | T | 78 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(75): Show | 78 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.306+1957_306+1958d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91975923 | |||||
| chr7:91975924
|
TG | T | 16 | a0002c0002t0002g0244a0003c0003t0002g0212a0003c0003t0002g0288others(13): Show | 16 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.306+1957delG | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975924 | ||||||
| chr7:91975925
|
G | GT | 9 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG00621.hp1 HG01081.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.306+1971dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91975925 | |||||
| chr7:91975925
|
G | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0117 | 3 | NA18940.hp2 NA18964.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.306+1957G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975925 | ||||||
| chr7:91975929
|
T | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.306+1961T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975929 | ||||||
| chr7:91975933
|
T | G | 2 | a0001c0001t0001g0046a0025c0026t0001g0075 | 2 | HG00673.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.306+1965T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91975933 | ||||||
| chr7:91976115
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.306+2147G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91976115 | ||||||
| chr7:91976411
|
C | T | 1 | a0016c0028t0001g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.306+2443C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91976411 | ||||||
| chr7:91976446
|
C | A | 1 | a0002c0002t0002g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.306+2478C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91976446 | ||||||
| chr7:91976470
|
G | A | 1 | a0002c0002t0002g0255 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.306+2502G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91976470 | ||||||
| chr7:91976690
|
C | T | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.306+2722C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91976690 | ||||||
| chr7:91976748
|
C | CTCT | 100 | a0001c0001t0001g0098a0002c0002t0002g0213a0002c0002t0002g0214others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.306+2783_306+2785d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91976748 | |||||
| chr7:91977047
|
C | T | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.306+3079C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977047 | ||||||
| chr7:91977188
|
A | T | 1 | a0005c0005t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.307-3101A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977188 | ||||||
| chr7:91977328
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.307-2961G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977328 | ||||||
| chr7:91977550
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.307-2739C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977550 | ||||||
| chr7:91977551
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.307-2738G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977551 | ||||||
| chr7:91977630
|
G | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 303 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.307-2659G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977630 | ||||||
| chr7:91977985
|
T | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-2304T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91977985 | ||||||
| chr7:91978163
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.307-2126A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978163 | ||||||
| chr7:91978223
|
CAG | C | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.307-2063_307-2062d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978223 | |||||
| chr7:91978241
|
C | CA | 6 | a0001c0001t0001g0102a0001c0001t0001g0104a0007c0007t0002g0287others(3): Show | 6 | HG02027.hp2 HG02040.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-2028dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978241 | |||||
| chr7:91978241
|
CA | C | 100 | a0001c0001t0001g0054a0001c0001t0001g0098a0001c0001t0001g0107others(97): Show | 100 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.307-2028delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978241 | |||||
| chr7:91978288
|
G | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-2001G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978288 | ||||||
| chr7:91978370
|
C | T | 1 | a0002c0002t0002g0220 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.307-1919C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978370 | ||||||
| chr7:91978538
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.307-1751C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978538 | ||||||
| chr7:91978647
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.307-1642A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978647 | ||||||
| chr7:91978840
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.307-1449T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978840 | ||||||
| chr7:91978875
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.307-1414G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978875 | ||||||
| chr7:91978929
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1360T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978929 | ||||||
| chr7:91978932
|
A | AT | 32 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0064others(29): Show | 32 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.307-1332dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978932 | |||||
| chr7:91978932
|
A | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG00673.hp2 HG02027.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.307-1357A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978932 | ||||||
| chr7:91978932
|
AT | A | 23 | a0001c0001t0001g0052a0001c0001t0001g0094a0001c0001t0001g0098others(20): Show | 23 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.307-1332delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978932 | |||||
| chr7:91978932
|
ATT | A | 81 | a0001c0001t0001g0121a0002c0002t0002g0213a0002c0002t0002g0214others(78): Show | 81 | HG00280.hp2 HG00639.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.307-1333_307-1332d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | INFO_REALIGN_3_PRIME | chr7 | 91978932 | |||||
| chr7:91978966
|
C | T | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.307-1323C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91978966 | ||||||
| chr7:91979095
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.307-1194G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979095 | ||||||
| chr7:91979104
|
G | A | 6 | a0002c0002t0002g0279a0002c0002t0002g0280a0002c0002t0002g0282others(3): Show | 6 | HG00642.hp1 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1185G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979104 | ||||||
| chr7:91979242
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.307-1047G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979242 | ||||||
| chr7:91979317
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.307-972A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979317 | ||||||
| chr7:91979483
|
A | G | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.307-806A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979483 | ||||||
| chr7:91979612
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-677G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979612 | ||||||
| chr7:91979716
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.307-573C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979716 | ||||||
| chr7:91979919
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-370C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 2/49 | chr7 | 91979919 | ||||||
| chr7:91980495
|
C | CTT | 12 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0001t0001g0137others(9): Show | 12 | HG00738.hp2 HG01256.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+184_351+185dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91980495 | |||||
| chr7:91980495
|
C | CTTT | 91 | a0001c0001t0001g0004a0001c0001t0001g0079a0001c0001t0001g0081others(88): Show | 91 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.351+183_351+185dup others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91980495 | |||||
| chr7:91980495
|
C | CTTTT | 40 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(37): Show | 40 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.351+182_351+185dup others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91980495 | |||||
| chr7:91980495
|
C | CTTTTT | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 126 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.351+181_351+185dup others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91980495 | |||||
| chr7:91980495
|
C | CTTTTTT | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0042others(29): Show | 32 | HG01081.hp1 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.351+180_351+185dup others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91980495 | |||||
| chr7:91980763
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.351+430A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91980763 | ||||||
| chr7:91980797
|
T | G | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.351+464T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91980797 | ||||||
| chr7:91981256
|
A | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0139 | 3 | NA18973.hp1 NA19070.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.351+923A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981256 | ||||||
| chr7:91981274
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.351+941C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981274 | ||||||
| chr7:91981444
|
T | C | 1 | a0002c0002t0002g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.351+1111T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981444 | ||||||
| chr7:91981603
|
CT | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 183 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.351+1290delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91981603 | |||||
| chr7:91981603
|
CTT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0085others(3): Show | 6 | HG01081.hp1 NA18942.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1289_351+1290d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91981603 | |||||
| chr7:91981648
|
T | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.351+1315T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981648 | ||||||
| chr7:91981810
|
T | C | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.351+1477T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981810 | ||||||
| chr7:91981840
|
A | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.351+1507A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981840 | ||||||
| chr7:91981987
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1654G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91981987 | ||||||
| chr7:91982150
|
C | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18942.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.351+1817C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982150 | ||||||
| chr7:91982166
|
C | CGTAT | 30 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00597.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.351+1871_351+1874d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91982166 | |||||
| chr7:91982166
|
C | CGTATGTA others(1): Show |
3 | a0001c0001t0001g0175a0002c0002t0003g0258a0002c0002t0003g0261 | 3 | HG01168.hp2 HG01169.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.351+1867_351+1874d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91982166 | |||||
| chr7:91982166
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+1833C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982166 | ||||||
| chr7:91982166
|
CGTAT | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0001g0090others(12): Show | 15 | HG00621.hp1 HG01081.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.351+1871_351+1874d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91982166 | |||||
| chr7:91982166
|
CGTATGTA others(9): Show |
C | 1 | a0001c0001t0001g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.351+1859_351+1874d others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91982166 | |||||
| chr7:91982166
|
CGTATGTA others(13): Show |
C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1855_351+1874d others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91982166 | |||||
| chr7:91982205
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.351+1872A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982205 | ||||||
| chr7:91982412
|
A | G | 1 | a0004c0004t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.351+2079A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982412 | ||||||
| chr7:91982428
|
G | A | 4 | a0002c0002t0002g0267a0002c0002t0002g0268a0002c0002t0002g0305others(1): Show | 4 | HG00735.hp1 HG01192.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2095G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982428 | ||||||
| chr7:91982437
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2104C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982437 | ||||||
| chr7:91982557
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.351+2224T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982557 | ||||||
| chr7:91982740
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.351+2407A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982740 | ||||||
| chr7:91982751
|
C | T | 1 | a0002c0002t0002g0273 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.351+2418C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982751 | ||||||
| chr7:91982937
|
C | T | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2604C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91982937 | ||||||
| chr7:91983255
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2922A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983255 | ||||||
| chr7:91983341
|
G | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.351+3008G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983341 | ||||||
| chr7:91983405
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.351+3072T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983405 | ||||||
| chr7:91983524
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+3191G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983524 | ||||||
| chr7:91983584
|
G | A | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.351+3251G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983584 | ||||||
| chr7:91983598
|
C | T | 1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.351+3265C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983598 | ||||||
| chr7:91983672
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.351+3339G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983672 | ||||||
| chr7:91983765
|
C | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.351+3432C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91983765 | ||||||
| chr7:91984038
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+3705G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984038 | ||||||
| chr7:91984095
|
G | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+3762G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984095 | ||||||
| chr7:91984129
|
A | C | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+3796A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984129 | ||||||
| chr7:91984139
|
C | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.351+3806C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984139 | ||||||
| chr7:91984191
|
C | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+3858C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984191 | ||||||
| chr7:91984207
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+3874A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984207 | ||||||
| chr7:91984499
|
T | C | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+4166T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984499 | ||||||
| chr7:91984678
|
A | G | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.351+4345A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984678 | ||||||
| chr7:91984694
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | NA18940.hp1 NA18999.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.351+4361G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91984694 | ||||||
| chr7:91984862
|
GATTCCTA others(8): Show |
G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+4534_351+4548d others(17): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91984862 | |||||
| chr7:91985043
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.351+4710A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985043 | ||||||
| chr7:91985065
|
A | C | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+4732A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985065 | ||||||
| chr7:91985077
|
C | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+4744C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985077 | ||||||
| chr7:91985098
|
C | T | 1 | a0005c0005t0001g0147 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.351+4765C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985098 | ||||||
| chr7:91985111
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.351+4778C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985111 | ||||||
| chr7:91985405
|
A | G | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+5072A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985405 | ||||||
| chr7:91985514
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.351+5181G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985514 | ||||||
| chr7:91985533
|
T | C | 1 | a0009c0012t0002g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.351+5200T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985533 | ||||||
| chr7:91985641
|
T | G | 1 | a0010c0010t0001g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.351+5308T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985641 | ||||||
| chr7:91985714
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.351+5381C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91985714 | ||||||
| chr7:91986014
|
T | C | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.351+5681T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986014 | ||||||
| chr7:91986086
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+5753A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986086 | ||||||
| chr7:91986105
|
G | T | 1 | a0002c0002t0002g0216 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.351+5772G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986105 | ||||||
| chr7:91986113
|
C | A | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.351+5780C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986113 | ||||||
| chr7:91986190
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+5857G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986190 | ||||||
| chr7:91986247
|
T | C | 1 | a0009c0012t0002g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-5911T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986247 | ||||||
| chr7:91986257
|
G | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-5901G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986257 | ||||||
| chr7:91986280
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.352-5878G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986280 | ||||||
| chr7:91986362
|
G | A | 1 | a0002c0002t0002g0220 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.352-5796G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986362 | ||||||
| chr7:91986467
|
G | A | 1 | a0002c0002t0002g0267 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.352-5691G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986467 | ||||||
| chr7:91986502
|
G | A | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.352-5656G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986502 | ||||||
| chr7:91986540
|
A | G | 1 | a0002c0002t0002g0253 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.352-5618A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986540 | ||||||
| chr7:91986615
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.352-5543A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986615 | ||||||
| chr7:91986871
|
C | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-5287C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986871 | ||||||
| chr7:91986921
|
T | C | 3 | a0001c0001t0001g0012a0001c0011t0001g0011a0001c0011t0001g0013 | 3 | HG03486.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.352-5237T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986921 | ||||||
| chr7:91986988
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.352-5170A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91986988 | ||||||
| chr7:91987108
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-5050A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987108 | ||||||
| chr7:91987260
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0041 | 2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.352-4898A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987260 | ||||||
| chr7:91987310
|
T | C | 1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.352-4848T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987310 | ||||||
| chr7:91987368
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352-4790G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987368 | ||||||
| chr7:91987420
|
G | A | 5 | a0002c0002t0002g0244a0002c0002t0002g0245a0002c0002t0002g0248others(2): Show | 5 | HG00639.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-4738G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987420 | ||||||
| chr7:91987577
|
G | A | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-4581G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987577 | ||||||
| chr7:91987608
|
T | C | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.352-4550T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987608 | ||||||
| chr7:91987777
|
C | G | 39 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(36): Show | 39 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.352-4381C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987777 | ||||||
| chr7:91987801
|
C | T | 14 | a0002c0002t0002g0273a0002c0002t0002g0274a0002c0002t0002g0276others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.352-4357C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91987801 | ||||||
| chr7:91988107
|
C | G | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.352-4051C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988107 | ||||||
| chr7:91988293
|
C | A | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.352-3865C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988293 | ||||||
| chr7:91988297
|
C | CA | 59 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0028others(56): Show | 59 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.352-3833dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91988297 | |||||
| chr7:91988297
|
CA | C | 82 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0121others(79): Show | 82 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.352-3833delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91988297 | |||||
| chr7:91988297
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.352-3843_352-3833d others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91988297 | |||||
| chr7:91988297
|
CAAAAAAA others(5): Show |
C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.352-3844_352-3833d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91988297 | |||||
| chr7:91988329
|
A | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.352-3829A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988329 | ||||||
| chr7:91988354
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.352-3804C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988354 | ||||||
| chr7:91988449
|
T | C | 1 | a0005c0005t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.352-3709T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988449 | ||||||
| chr7:91988520
|
C | T | 3 | a0001c0008t0001g0091a0001c0008t0001g0188a0001c0008t0001g0189 | 3 | NA18747.hp1 NA19074.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.352-3638C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988520 | ||||||
| chr7:91988852
|
G | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-3306G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988852 | ||||||
| chr7:91988894
|
T | C | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-3264T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91988894 | ||||||
| chr7:91989140
|
TAATA | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.352-3014_352-3011d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91989140 | |||||
| chr7:91989433
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-2725G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91989433 | ||||||
| chr7:91989474
|
T | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-2684T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91989474 | ||||||
| chr7:91989476
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.352-2682T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91989476 | ||||||
| chr7:91990205
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.352-1953A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990205 | ||||||
| chr7:91990402
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.352-1756G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990402 | ||||||
| chr7:91990487
|
T | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.352-1671T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990487 | ||||||
| chr7:91990655
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1503A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990655 | ||||||
| chr7:91990782
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.352-1376G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990782 | ||||||
| chr7:91990978
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1180A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91990978 | ||||||
| chr7:91991297
|
C | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-861C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991297 | ||||||
| chr7:91991305
|
T | TA | 99 | a0001c0001t0001g0047a0002c0002t0002g0213a0002c0002t0002g0214others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.352-846dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91991305 | |||||
| chr7:91991472
|
C | CT | 8 | a0001c0001t0001g0142a0003c0003t0002g0293a0007c0007t0002g0287others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-669dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | INFO_REALIGN_3_PRIME | chr7 | 91991472 | |||||
| chr7:91991511
|
G | T | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.352-647G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991511 | ||||||
| chr7:91991557
|
C | T | 94 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(91): Show | 94 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.352-601C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991557 | ||||||
| chr7:91991633
|
G | A | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-525G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991633 | ||||||
| chr7:91991673
|
G | A | 1 | a0002c0002t0002g0236 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.352-485G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991673 | ||||||
| chr7:91991693
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.352-465G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991693 | ||||||
| chr7:91991842
|
T | C | 1 | a0004c0004t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.352-316T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991842 | ||||||
| chr7:91991952
|
A | T | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.352-206A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91991952 | ||||||
| chr7:91992003
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-155A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 3/49 | chr7 | 91992003 | ||||||
| chr7:91992461
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405+250C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | chr7 | 91992461 | ||||||
| chr7:91992534
|
G | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+323G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | chr7 | 91992534 | ||||||
| chr7:91992620
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.406-265C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | chr7 | 91992620 | ||||||
| chr7:91992661
|
C | CA | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(75): Show | 78 | HG00558.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.406-200dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | INFO_REALIGN_3_PRIME | chr7 | 91992661 | |||||
| chr7:91992661
|
C | CAA | 14 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(11): Show | 14 | HG00423.hp1 HG00673.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.406-201_406-200dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | INFO_REALIGN_3_PRIME | chr7 | 91992661 | |||||
| chr7:91992678
|
A | AAC | 9 | a0002c0002t0002g0213a0002c0002t0002g0227a0002c0002t0002g0230others(6): Show | 9 | HG01981.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.406-206_406-205ins others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | INFO_REALIGN_3_PRIME | chr7 | 91992678 | |||||
| chr7:91992678
|
A | AC | 84 | a0002c0002t0002g0214a0002c0002t0002g0215a0002c0002t0002g0216others(81): Show | 84 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.406-207_406-206ins others(1): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | chr7 | 91992678 | ||||||
| chr7:91992678
|
A | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.406-207A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 4/49 | chr7 | 91992678 | ||||||
| chr7:91993151
|
T | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.576+96T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993151 | ||||||
| chr7:91993176
|
TTTC | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0011t0001g0011others(2): Show | 5 | HG03486.hp1 HG03834.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+139_576+141del others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | INFO_REALIGN_3_PRIME | chr7 | 91993176 | |||||
| chr7:91993362
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.576+307G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993362 | ||||||
| chr7:91993476
|
C | T | 1 | a0016c0028t0001g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.576+421C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993476 | ||||||
| chr7:91993570
|
G | A | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+515G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993570 | ||||||
| chr7:91993683
|
ATTTCATT others(3): Show |
A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.576+629_576+638del others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993683 | ||||||
| chr7:91993730
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.576+675G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91993730 | ||||||
| chr7:91994498
|
G | T | 1 | a0001c0011t0001g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.577-123G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 5/49 | chr7 | 91994498 | ||||||
| chr7:91994863
|
A | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0045 | 2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.732+87A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 6/49 | chr7 | 91994863 | ||||||
| chr7:91994923
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.732+147A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 6/49 | chr7 | 91994923 | ||||||
| chr7:91995116
|
A | G | 2 | a0001c0001t0001g0042a0001c0018t0001g0010 | 2 | NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.732+340A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 6/49 | chr7 | 91995116 | ||||||
| chr7:91995488
|
G | A | 1 | a0002c0002t0002g0219 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.733-115G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 6/49 | chr7 | 91995488 | ||||||
| chr7:91995576
|
C | T | 1 | a0004c0004t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733-27C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 6/49 | chr7 | 91995576 | ||||||
| chr7:91995954
|
G | GTAATGTA others(3): Show |
1 | a0013c0031t0002g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.930+156_930+165dup others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91995954 | |||||
| chr7:91995977
|
G | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.930+177G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91995977 | ||||||
| chr7:91996113
|
A | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.930+313A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996113 | ||||||
| chr7:91996295
|
G | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0021others(9): Show | 12 | HG00621.hp2 HG02056.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.930+495G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996295 | ||||||
| chr7:91996317
|
T | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.930+517T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996317 | ||||||
| chr7:91996458
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.930+658C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996458 | ||||||
| chr7:91996649
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+849C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996649 | ||||||
| chr7:91996740
|
A | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.930+940A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996740 | ||||||
| chr7:91996770
|
C | T | 1 | a0002c0002t0002g0263 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.930+970C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91996770 | ||||||
| chr7:91997087
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.930+1287G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997087 | ||||||
| chr7:91997307
|
C | T | 1 | a0002c0002t0002g0238 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.930+1507C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997307 | ||||||
| chr7:91997385
|
T | G | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.930+1585T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997385 | ||||||
| chr7:91997538
|
G | A | 1 | a0002c0002t0002g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.930+1738G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997538 | ||||||
| chr7:91997601
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.930+1801A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997601 | ||||||
| chr7:91997639
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.930+1839A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997639 | ||||||
| chr7:91997853
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.930+2053A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997853 | ||||||
| chr7:91997920
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 303 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.930+2120T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997920 | ||||||
| chr7:91997983
|
T | A | 2 | a0002c0002t0002g0245a0002c0002t0002g0248 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.930+2183T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91997983 | ||||||
| chr7:91998154
|
A | C | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.930+2354A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998154 | ||||||
| chr7:91998186
|
C | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.930+2386C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998186 | ||||||
| chr7:91998187
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+2387G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998187 | ||||||
| chr7:91998375
|
C | T | 1 | a0005c0005t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.931-2473C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998375 | ||||||
| chr7:91998418
|
C | CT | 23 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0086others(20): Show | 23 | HG00423.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.931-2393dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
C | CTT | 41 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0096others(38): Show | 41 | HG00280.hp1 HG00621.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.931-2394_931-2393d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
C | CTTT | 31 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0084others(28): Show | 31 | HG00558.hp1 HG00735.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.931-2395_931-2393d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
C | CTTTT | 9 | a0001c0001t0001g0089a0001c0001t0001g0125a0001c0001t0001g0132others(6): Show | 9 | HG00597.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.931-2396_931-2393d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTT | C | 15 | a0002c0002t0002g0215a0002c0002t0002g0219a0002c0002t0002g0228others(12): Show | 15 | HG00738.hp1 HG01928.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.931-2398_931-2393d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT | C | 64 | a0002c0002t0002g0213a0002c0002t0002g0216a0002c0002t0002g0220others(61): Show | 64 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.931-2399_931-2393d others(9): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(1): Show |
C | 15 | a0002c0002t0002g0214a0002c0002t0002g0231a0002c0002t0002g0234others(12): Show | 15 | HG01070.hp1 HG01074.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.931-2400_931-2393d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(5): Show |
C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-2404_931-2393d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(8): Show |
C | 15 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(12): Show | 15 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.931-2407_931-2393d others(17): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(9): Show |
C | 1 | a0004c0004t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.931-2408_931-2393d others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0056 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.931-2409_931-2393d others(19): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998418
|
CTTTTTTT others(11): Show |
C | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.931-2410_931-2393d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91998418 | |||||
| chr7:91998638
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.931-2210C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998638 | ||||||
| chr7:91998735
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0032others(6): Show | 9 | HG00558.hp2 HG02083.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.931-2113A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998735 | ||||||
| chr7:91998798
|
T | A | 1 | a0002c0002t0002g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.931-2050T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91998798 | ||||||
| chr7:91999091
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.931-1757T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999091 | ||||||
| chr7:91999161
|
T | C | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-1687T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999161 | ||||||
| chr7:91999166
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.931-1682T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999166 | ||||||
| chr7:91999224
|
T | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.931-1624T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999224 | ||||||
| chr7:91999256
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.931-1592C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999256 | ||||||
| chr7:91999279
|
G | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.931-1569G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999279 | ||||||
| chr7:91999436
|
T | C | 5 | a0002c0002t0002g0244a0002c0002t0002g0245a0002c0002t0002g0248others(2): Show | 5 | HG00639.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-1412T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999436 | ||||||
| chr7:91999837
|
A | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.931-1011A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 91999837 | ||||||
| chr7:91999854
|
G | GTTCA | 93 | a0001c0001t0001g0083a0002c0002t0002g0213a0002c0002t0002g0214others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.931-969_931-966dup others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91999854 | |||||
| chr7:91999854
|
GTTCA | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0109others(1): Show | 4 | HG01109.hp2 NA18939.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-969_931-966del others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | INFO_REALIGN_3_PRIME | chr7 | 91999854 | |||||
| chr7:92000209
|
A | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.931-639A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000209 | ||||||
| chr7:92000448
|
C | T | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.931-400C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000448 | ||||||
| chr7:92000670
|
T | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.931-178T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000670 | ||||||
| chr7:92000680
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0044 | 2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.931-168T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000680 | ||||||
| chr7:92000687
|
G | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.931-161G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000687 | ||||||
| chr7:92000692
|
T | C | 1 | a0018c0023t0001g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.931-156T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000692 | ||||||
| chr7:92000832
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.931-16A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 7/49 | chr7 | 92000832 | ||||||
| chr7:92003248
|
C | A | 11 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(8): Show | 11 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.3318+13C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92003248 | ||||||
| chr7:92003345
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3318+110A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92003345 | ||||||
| chr7:92003599
|
G | C | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3318+364G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92003599 | ||||||
| chr7:92003646
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3318+411A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92003646 | ||||||
| chr7:92003899
|
T | G | 97 | a0001c0001t0001g0124a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.3318+664T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92003899 | ||||||
| chr7:92004073
|
T | G | 4 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+838T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004073 | ||||||
| chr7:92004330
|
ATTCTGTG others(11): Show |
A | 2 | a0010c0010t0001g0191a0010c0010t0001g0195 | 2 | HG03688.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.3318+1115_3318+113 others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92004330 | |||||
| chr7:92004417
|
A | G | 1 | a0002c0002t0002g0255 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3318+1182A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004417 | ||||||
| chr7:92004501
|
C | G | 8 | a0001c0001t0001g0124a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3318+1266C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004501 | ||||||
| chr7:92004525
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3318+1290C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004525 | ||||||
| chr7:92004728
|
G | A | 9 | a0001c0001t0001g0124a0003c0003t0002g0288a0003c0003t0002g0289others(6): Show | 9 | HG00738.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3318+1493G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004728 | ||||||
| chr7:92004761
|
A | G | 2 | a0002c0002t0002g0277a0002c0002t0002g0281 | 2 | HG01346.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3318+1526A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004761 | ||||||
| chr7:92004812
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3318+1577T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004812 | ||||||
| chr7:92004828
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3318+1593T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004828 | ||||||
| chr7:92004918
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3318+1683G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92004918 | ||||||
| chr7:92005045
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3318+1810C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005045 | ||||||
| chr7:92005046
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3318+1811C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005046 | ||||||
| chr7:92005138
|
T | G | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3318+1903T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005138 | ||||||
| chr7:92005649
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3318+2414G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005649 | ||||||
| chr7:92005709
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3318+2474G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005709 | ||||||
| chr7:92005746
|
A | G | 1 | a0005c0005t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3318+2511A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005746 | ||||||
| chr7:92005813
|
GCAC | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3318+2588_3318+259 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92005813 | |||||
| chr7:92005844
|
T | A | 13 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(10): Show | 13 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.3318+2609T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005844 | ||||||
| chr7:92005852
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3318+2617A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92005852 | ||||||
| chr7:92006203
|
T | C | 4 | a0002c0002t0002g0254a0002c0002t0002g0255a0002c0002t0002g0256others(1): Show | 4 | HG00673.hp1 NA19064.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+2968T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006203 | ||||||
| chr7:92006211
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3318+2976C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006211 | ||||||
| chr7:92006305
|
A | T | 1 | a0002c0033t0002g0275 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3318+3070A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006305 | ||||||
| chr7:92006506
|
A | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3318+3271A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006506 | ||||||
| chr7:92006754
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0076 | 2 | HG01109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3318+3519C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006754 | ||||||
| chr7:92006762
|
T | G | 1 | a0016c0028t0001g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3318+3527T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006762 | ||||||
| chr7:92006768
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+3533G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006768 | ||||||
| chr7:92006876
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3318+3641A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92006876 | ||||||
| chr7:92007050
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+3815G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007050 | ||||||
| chr7:92007094
|
T | C | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3318+3859T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007094 | ||||||
| chr7:92007169
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+3934C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007169 | ||||||
| chr7:92007281
|
C | CT | 7 | a0001c0001t0001g0168a0004c0004t0001g0196a0004c0004t0001g0199others(4): Show | 7 | HG02129.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3318+4075dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92007281 | |||||
| chr7:92007281
|
CT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.3318+4075delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92007281 | |||||
| chr7:92007281
|
CTTTTTTT others(2): Show |
C | 90 | a0002c0002t0002g0214a0002c0002t0002g0215a0002c0002t0002g0216others(87): Show | 90 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.3318+4067_3318+407 others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92007281 | |||||
| chr7:92007281
|
CTTTTTTT others(3): Show |
C | 4 | a0002c0002t0002g0213a0002c0002t0002g0273a0002c0033t0002g0275others(1): Show | 4 | HG01070.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+4066_3318+407 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92007281 | |||||
| chr7:92007281
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0039 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3318+4063_3318+407 others(17): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92007281 | |||||
| chr7:92007282
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3318+4047T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007282 | ||||||
| chr7:92007347
|
G | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3318+4112G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007347 | ||||||
| chr7:92007696
|
G | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3318+4461G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007696 | ||||||
| chr7:92007710
|
T | A | 2 | a0003c0003t0002g0212a0028c0014t0002g0208 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3318+4475T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92007710 | ||||||
| chr7:92008224
|
G | A | 1 | a0026c0015t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3319-4205G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008224 | ||||||
| chr7:92008346
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3319-4083G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008346 | ||||||
| chr7:92008421
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3319-4008C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008421 | ||||||
| chr7:92008542
|
C | G | 1 | a0005c0005t0001g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3319-3887C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008542 | ||||||
| chr7:92008862
|
T | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3319-3567T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008862 | ||||||
| chr7:92008912
|
G | A | 1 | a0017c0025t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3319-3517G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008912 | ||||||
| chr7:92008939
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3319-3490T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92008939 | ||||||
| chr7:92008983
|
T | TA | 93 | a0001c0001t0001g0021a0001c0001t0001g0023a0002c0002t0002g0213others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3319-3429dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92008983 | |||||
| chr7:92008983
|
T | TAA | 6 | a0002c0002t0002g0227a0002c0002t0002g0237a0007c0007t0002g0287others(3): Show | 6 | HG01981.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3319-3430_3319-342 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | INFO_REALIGN_3_PRIME | chr7 | 92008983 | |||||
| chr7:92009061
|
A | G | 1 | a0002c0002t0002g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3319-3368A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009061 | ||||||
| chr7:92009137
|
A | G | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3319-3292A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009137 | ||||||
| chr7:92009306
|
G | C | 56 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.3319-3123G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009306 | ||||||
| chr7:92009578
|
G | A | 1 | a0026c0015t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3319-2851G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009578 | ||||||
| chr7:92009728
|
T | C | 1 | a0001c0008t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3319-2701T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009728 | ||||||
| chr7:92009805
|
T | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3319-2624T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009805 | ||||||
| chr7:92009999
|
C | T | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3319-2430C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92009999 | ||||||
| chr7:92010088
|
G | A | 1 | a0005c0005t0001g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3319-2341G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010088 | ||||||
| chr7:92010105
|
G | A | 1 | a0002c0002t0002g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3319-2324G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010105 | ||||||
| chr7:92010128
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3319-2301C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010128 | ||||||
| chr7:92010278
|
G | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3319-2151G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010278 | ||||||
| chr7:92010367
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3319-2062A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010367 | ||||||
| chr7:92010481
|
G | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3319-1948G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010481 | ||||||
| chr7:92010528
|
C | T | 2 | a0005c0005t0001g0129a0024c0017t0001g0149 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3319-1901C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010528 | ||||||
| chr7:92010855
|
G | C | 1 | a0027c0027t0001g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3319-1574G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010855 | ||||||
| chr7:92010954
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3319-1475A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010954 | ||||||
| chr7:92010959
|
G | A | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.3319-1470G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010959 | ||||||
| chr7:92010989
|
A | G | 1 | a0010c0010t0001g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3319-1440A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92010989 | ||||||
| chr7:92011058
|
C | T | 1 | a0004c0004t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3319-1371C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92011058 | ||||||
| chr7:92011082
|
A | G | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3319-1347A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92011082 | ||||||
| chr7:92011459
|
A | T | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3319-970A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92011459 | ||||||
| chr7:92011666
|
C | T | 1 | a0002c0002t0002g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3319-763C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92011666 | ||||||
| chr7:92012215
|
A | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3319-214A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92012215 | ||||||
| chr7:92012281
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3319-148A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92012281 | ||||||
| chr7:92012375
|
T | C | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3319-54T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 8/49 | chr7 | 92012375 | ||||||
| chr7:92012663
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3532+21T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012663 | ||||||
| chr7:92012664
|
A | G | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3532+22A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012664 | ||||||
| chr7:92012680
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3532+38A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012680 | ||||||
| chr7:92012794
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0036others(7): Show | 10 | NA18952.hp1 NA18962.hp2 NA18972.hp2 others(7): Show |
intron_variant | MODIFIER | c.3532+152C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012794 | ||||||
| chr7:92012942
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3532+300G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012942 | ||||||
| chr7:92012966
|
G | A | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3532+324G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92012966 | ||||||
| chr7:92012973
|
A | AT | 69 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0064others(66): Show | 69 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.3532+367dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATT | 45 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(42): Show | 45 | HG01261.hp2 HG01358.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.3532+366_3532+367d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTT | 23 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(20): Show | 23 | HG00423.hp1 HG00558.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.3532+365_3532+367d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTT | 11 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0040others(8): Show | 11 | HG00673.hp2 HG02027.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.3532+364_3532+367d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTTT | 6 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0037others(3): Show | 6 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3532+363_3532+367d others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0009a0028c0014t0002g0208 | 2 | HG02056.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3532+358_3532+367d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0067a0003c0003t0002g0212 | 2 | HG02647.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3532+357_3532+367d others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTTTTT others(6): Show |
1 | a0005c0005t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3532+355_3532+367d others(15): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3532+346_3532+367d others(24): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
AT | A | 36 | a0001c0001t0001g0119a0002c0002t0002g0221a0002c0002t0002g0231others(33): Show | 36 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.3532+367delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
ATTTTTTT others(7): Show |
A | 1 | a0002c0002t0002g0220 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3532+354_3532+367d others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0001g0029a0001c0001t0001g0170 | 2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3532+351_3532+367d others(19): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
ATTTTTTT others(11): Show |
A | 2 | a0001c0001t0001g0118a0005c0005t0001g0154 | 2 | HG00621.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3532+350_3532+367d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
ATTTTTTT others(12): Show |
A | 1 | a0005c0005t0001g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3532+349_3532+367d others(21): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92012973
|
ATTTTTTT others(14): Show |
A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3532+347_3532+367d others(23): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92012973 | |||||
| chr7:92013188
|
T | C | 1 | a0004c0004t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3532+546T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013188 | ||||||
| chr7:92013400
|
T | C | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3532+758T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013400 | ||||||
| chr7:92013441
|
A | T | 1 | a0013c0031t0002g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3532+799A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013441 | ||||||
| chr7:92013588
|
G | A | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3533-661G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013588 | ||||||
| chr7:92013873
|
AT | A | 93 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3533-371delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92013873 | |||||
| chr7:92013873
|
ATT | A | 3 | a0002c0002t0002g0244a0002c0002t0002g0263a0003c0003t0002g0289 | 3 | HG02559.hp2 HG02895.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.3533-372_3533-371d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | INFO_REALIGN_3_PRIME | chr7 | 92013873 | |||||
| chr7:92013878
|
T | A | 96 | a0001c0001t0001g0060a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3533-371T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013878 | ||||||
| chr7:92013890
|
C | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3533-359C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013890 | ||||||
| chr7:92013905
|
G | A | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.3533-344G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013905 | ||||||
| chr7:92013937
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3533-312A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92013937 | ||||||
| chr7:92014088
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.3533-161G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92014088 | ||||||
| chr7:92014101
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3533-148T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 9/49 | chr7 | 92014101 | ||||||
| chr7:92014379
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3612+51T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92014379 | ||||||
| chr7:92014444
|
G | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3612+116G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92014444 | ||||||
| chr7:92014453
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3612+125C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92014453 | ||||||
| chr7:92014531
|
AGGCATTG others(5): Show |
A | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3612+205_3612+216d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | INFO_REALIGN_3_PRIME | chr7 | 92014531 | |||||
| chr7:92014756
|
C | T | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.3612+428C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92014756 | ||||||
| chr7:92015027
|
C | G | 75 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(72): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.3612+699C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015027 | ||||||
| chr7:92015239
|
A | G | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.3613-890A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015239 | ||||||
| chr7:92015299
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.3613-830C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015299 | ||||||
| chr7:92015302
|
G | A | 2 | a0003c0003t0002g0212a0028c0014t0002g0208 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3613-827G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015302 | ||||||
| chr7:92015366
|
A | AT | 50 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0057others(47): Show | 50 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.3613-745dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | INFO_REALIGN_3_PRIME | chr7 | 92015366 | |||||
| chr7:92015366
|
AT | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(105): Show | 108 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.3613-745delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | INFO_REALIGN_3_PRIME | chr7 | 92015366 | |||||
| chr7:92015520
|
C | T | 9 | a0002c0002t0002g0220a0002c0002t0002g0223a0002c0002t0002g0226others(6): Show | 9 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3613-609C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015520 | ||||||
| chr7:92015521
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3613-608G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015521 | ||||||
| chr7:92015767
|
C | A | 1 | a0002c0002t0002g0219 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3613-362C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015767 | ||||||
| chr7:92015838
|
G | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3613-291G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015838 | ||||||
| chr7:92015933
|
A | G | 1 | a0002c0002t0002g0267 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3613-196A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015933 | ||||||
| chr7:92015951
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3613-178A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92015951 | ||||||
| chr7:92016001
|
G | A | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3613-128G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 10/49 | chr7 | 92016001 | ||||||
| chr7:92016479
|
G | T | 9 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0002g0244others(6): Show | 9 | HG00639.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3751+212G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 11/49 | chr7 | 92016479 | ||||||
| chr7:92016579
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3751+312T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 11/49 | chr7 | 92016579 | ||||||
| chr7:92016884
|
C | T | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.3752-133C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 11/49 | chr7 | 92016884 | ||||||
| chr7:92016889
|
A | G | 26 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(23): Show | 26 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.3752-128A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 11/49 | chr7 | 92016889 | ||||||
| chr7:92017222
|
A | G | 1 | a0003c0003t0002g0295 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3837+120A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017222 | ||||||
| chr7:92017262
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3837+160A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017262 | ||||||
| chr7:92017285
|
G | A | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.3837+183G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017285 | ||||||
| chr7:92017439
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3837+337T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017439 | ||||||
| chr7:92017657
|
A | G | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3837+555A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017657 | ||||||
| chr7:92017727
|
A | T | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3837+625A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017727 | ||||||
| chr7:92017823
|
C | T | 56 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.3837+721C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017823 | ||||||
| chr7:92017995
|
G | A | 1 | a0002c0002t0002g0284 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3837+893G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92017995 | ||||||
| chr7:92018001
|
G | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02155.hp2 NA19001.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.3837+899G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018001 | ||||||
| chr7:92018076
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3837+974A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018076 | ||||||
| chr7:92018284
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3837+1182C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018284 | ||||||
| chr7:92018331
|
C | T | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3837+1229C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018331 | ||||||
| chr7:92018395
|
A | AAC | 11 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0124others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3837+1339_3837+134 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACAC | 6 | a0001c0001t0001g0089a0001c0001t0001g0133a0001c0001t0001g0136others(3): Show | 6 | HG01081.hp2 HG02602.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.3837+1337_3837+134 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACAC | 9 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG00642.hp2 HG01168.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3837+1335_3837+134 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACACA others(1): Show |
13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG01070.hp2 HG01106.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3837+1333_3837+134 others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACACA others(3): Show |
10 | a0001c0001t0001g0096a0001c0001t0001g0131a0001c0001t0001g0137others(7): Show | 10 | HG00280.hp1 HG00597.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3837+1331_3837+134 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACACA others(5): Show |
6 | a0001c0001t0001g0079a0001c0001t0001g0097a0001c0001t0001g0138others(3): Show | 6 | HG02717.hp2 HG02723.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.3837+1329_3837+134 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACACA others(7): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0162a0001c0008t0001g0189 | 3 | NA18977.hp2 NA19003.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3837+1327_3837+134 others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3837+1325_3837+134 others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AAC | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(26): Show | 29 | HG00597.hp2 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.3837+1339_3837+134 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AACAC | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 43 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.3837+1337_3837+134 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AACACAC | A | 3 | a0001c0001t0001g0095a0004c0004t0001g0192a0010c0010t0001g0191 | 3 | HG04228.hp2 NA19086.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3837+1335_3837+134 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AACACACA others(1): Show |
A | 13 | a0001c0001t0001g0073a0004c0004t0001g0196a0004c0004t0001g0197others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.3837+1333_3837+134 others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AACACACA others(3): Show |
A | 2 | a0004c0004t0001g0194a0025c0026t0001g0075 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3837+1331_3837+134 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018395
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3837+1329_3837+134 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018395 | |||||
| chr7:92018433
|
CACACACA others(3): Show |
C | 5 | a0002c0002t0002g0256a0007c0007t0002g0287a0007c0007t0002g0302others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3837+1333_3837+134 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018433 | |||||
| chr7:92018435
|
C | CACAT | 41 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.3837+1336_3837+133 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018435 | |||||
| chr7:92018435
|
CACACACA others(1): Show |
C | 60 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(57): Show | 60 | HG00642.hp1 HG00673.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.3837+1335_3837+134 others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018435 | |||||
| chr7:92018437
|
CACACAG | C | 19 | a0002c0002t0002g0220a0002c0002t0002g0223a0002c0002t0002g0225others(16): Show | 19 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.3837+1337_3837+134 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018437 | |||||
| chr7:92018439
|
CACAG | C | 4 | a0002c0002t0002g0221a0002c0002t0002g0249a0003c0003t0002g0295others(1): Show | 4 | HG00639.hp2 HG02559.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3837+1339_3837+134 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018439 | |||||
| chr7:92018441
|
CAG | C | 7 | a0003c0003t0002g0290a0003c0003t0002g0291a0003c0003t0002g0294others(4): Show | 7 | HG00738.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3837+1343_3837+134 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | INFO_REALIGN_3_PRIME | chr7 | 92018441 | |||||
| chr7:92018443
|
G | C | 4 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0292others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3837+1341G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018443 | ||||||
| chr7:92018451
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3837+1349T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018451 | ||||||
| chr7:92018474
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3837+1372A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018474 | ||||||
| chr7:92018913
|
A | G | 1 | a0002c0033t0002g0275 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3837+1811A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92018913 | ||||||
| chr7:92019027
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3837+1925G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019027 | ||||||
| chr7:92019109
|
A | G | 1 | a0004c0004t0001g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3837+2007A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019109 | ||||||
| chr7:92019271
|
A | G | 1 | a0002c0002t0002g0299 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3837+2169A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019271 | ||||||
| chr7:92019301
|
C | A | 1 | a0010c0010t0001g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3837+2199C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019301 | ||||||
| chr7:92019335
|
T | A | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3837+2233T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019335 | ||||||
| chr7:92019414
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3837+2312A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019414 | ||||||
| chr7:92019430
|
A | G | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3837+2328A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019430 | ||||||
| chr7:92019625
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.3837+2523A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019625 | ||||||
| chr7:92019687
|
T | G | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3838-2551T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019687 | ||||||
| chr7:92019921
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.3838-2317A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019921 | ||||||
| chr7:92019948
|
A | T | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3838-2290A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92019948 | ||||||
| chr7:92020183
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3838-2055G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020183 | ||||||
| chr7:92020394
|
G | A | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3838-1844G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020394 | ||||||
| chr7:92020459
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3838-1779C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020459 | ||||||
| chr7:92020528
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3838-1710T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020528 | ||||||
| chr7:92020594
|
A | G | 4 | a0001c0001t0001g0012a0001c0011t0001g0011a0001c0011t0001g0013others(1): Show | 4 | HG02258.hp2 HG03486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3838-1644A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020594 | ||||||
| chr7:92020773
|
C | T | 1 | a0002c0002t0002g0255 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3838-1465C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92020773 | ||||||
| chr7:92021247
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3838-991G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92021247 | ||||||
| chr7:92021862
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01081.hp1 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3838-376G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92021862 | ||||||
| chr7:92022069
|
T | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3838-169T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 12/49 | chr7 | 92022069 | ||||||
| chr7:92022401
|
G | T | 1 | a0005c0005t0001g0147 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3952+49G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 13/49 | chr7 | 92022401 | ||||||
| chr7:92022459
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3952+107C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 13/49 | chr7 | 92022459 | ||||||
| chr7:92023260
|
G | A | 2 | a0005c0005t0001g0154a0005c0005t0001g0155 | 2 | NA18747.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.4148+251G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92023260 | ||||||
| chr7:92023449
|
T | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4148+440T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92023449 | ||||||
| chr7:92023486
|
G | A | 1 | a0003c0003t0002g0295 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4148+477G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92023486 | ||||||
| chr7:92024184
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4148+1175G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024184 | ||||||
| chr7:92024417
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4148+1408T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024417 | ||||||
| chr7:92024429
|
A | ATG | 6 | a0003c0003t0002g0212a0007c0007t0002g0287a0007c0007t0002g0302others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4148+1430_4148+143 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92024429 | |||||
| chr7:92024429
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4148+1420A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024429 | ||||||
| chr7:92024439
|
G | GTA | 35 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(32): Show | 35 | HG00639.hp2 HG01358.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.4148+1444_4148+144 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92024439 | |||||
| chr7:92024439
|
G | GTATA | 37 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0253others(34): Show | 37 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.4148+1442_4148+144 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92024439 | |||||
| chr7:92024439
|
G | GTATATA | 3 | a0002c0002t0002g0255a0002c0002t0002g0300a0002c0033t0002g0275 | 3 | HG00673.hp1 HG01070.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.4148+1440_4148+144 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92024439 | |||||
| chr7:92024453
|
A | T | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4148+1444A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024453 | ||||||
| chr7:92024493
|
A | G | 3 | a0006c0006t0001g0200a0006c0006t0001g0203a0006c0006t0001g0204 | 3 | HG01884.hp1 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4148+1484A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024493 | ||||||
| chr7:92024537
|
T | G | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.4148+1528T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024537 | ||||||
| chr7:92024814
|
C | G | 1 | a0002c0002t0002g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4148+1805C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024814 | ||||||
| chr7:92024814
|
C | T | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4148+1805C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024814 | ||||||
| chr7:92024943
|
A | G | 2 | a0002c0002t0002g0251a0002c0002t0002g0299 | 2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.4148+1934A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92024943 | ||||||
| chr7:92025111
|
A | G | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4148+2102A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025111 | ||||||
| chr7:92025150
|
T | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4148+2141T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025150 | ||||||
| chr7:92025151
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4148+2142G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025151 | ||||||
| chr7:92025203
|
G | A | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.4148+2194G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025203 | ||||||
| chr7:92025303
|
C | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.4148+2294C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025303 | ||||||
| chr7:92025304
|
A | G | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.4148+2295A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025304 | ||||||
| chr7:92025324
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4148+2315G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025324 | ||||||
| chr7:92025458
|
A | G | 2 | a0002c0002t0002g0251a0002c0002t0002g0299 | 2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.4148+2449A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025458 | ||||||
| chr7:92025465
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4148+2456T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025465 | ||||||
| chr7:92025490
|
G | C | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4148+2481G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025490 | ||||||
| chr7:92025817
|
G | A | 1 | a0005c0005t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4148+2808G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025817 | ||||||
| chr7:92025985
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4148+2976G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92025985 | ||||||
| chr7:92026015
|
A | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4148+3006A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026015 | ||||||
| chr7:92026032
|
A | C | 1 | a0002c0002t0002g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4148+3023A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026032 | ||||||
| chr7:92026299
|
A | G | 1 | a0002c0002t0002g0260 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4148+3290A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026299 | ||||||
| chr7:92026358
|
A | G | 22 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0096others(19): Show | 22 | HG00597.hp1 HG02523.hp1 NA18747.hp1 others(19): Show |
intron_variant | MODIFIER | c.4148+3349A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026358 | ||||||
| chr7:92026377
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4148+3368G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026377 | ||||||
| chr7:92026408
|
C | T | 11 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(8): Show | 11 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.4148+3399C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026408 | ||||||
| chr7:92026487
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4149-3408G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026487 | ||||||
| chr7:92026524
|
G | A | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4149-3371G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026524 | ||||||
| chr7:92026639
|
A | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4149-3256A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026639 | ||||||
| chr7:92026646
|
C | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4149-3249C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026646 | ||||||
| chr7:92026659
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4149-3236C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026659 | ||||||
| chr7:92026798
|
C | G | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4149-3097C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026798 | ||||||
| chr7:92026872
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4149-3023C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026872 | ||||||
| chr7:92026891
|
A | C | 1 | a0002c0002t0002g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4149-3004A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026891 | ||||||
| chr7:92026955
|
G | C | 1 | a0005c0005t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4149-2940G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92026955 | ||||||
| chr7:92027043
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4149-2852G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027043 | ||||||
| chr7:92027157
|
G | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4149-2738G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027157 | ||||||
| chr7:92027193
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.4149-2702T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027193 | ||||||
| chr7:92027201
|
C | T | 1 | a0001c0011t0001g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4149-2694C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027201 | ||||||
| chr7:92027269
|
T | C | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4149-2626T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027269 | ||||||
| chr7:92027286
|
G | A | 11 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(8): Show | 11 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.4149-2609G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027286 | ||||||
| chr7:92027321
|
A | AC | 5 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0089others(2): Show | 5 | HG01109.hp2 HG04115.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.4149-2570dupC | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92027321 | |||||
| chr7:92027326
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4149-2569G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027326 | ||||||
| chr7:92027362
|
CGTCTGGG others(30): Show |
C | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4149-2526_4149-249 others(41): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92027362 | |||||
| chr7:92027390
|
C | T | 1 | a0005c0005t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4149-2505C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027390 | ||||||
| chr7:92027431
|
C | T | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4149-2464C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027431 | ||||||
| chr7:92027515
|
G | A | 1 | a0001c0008t0001g0188 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4149-2380G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027515 | ||||||
| chr7:92027532
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4149-2363C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027532 | ||||||
| chr7:92027552
|
G | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4149-2343G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027552 | ||||||
| chr7:92027583
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4149-2312T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027583 | ||||||
| chr7:92027597
|
AGTGAGGA others(30): Show |
A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4149-2198_4149-216 others(41): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92027597 | |||||
| chr7:92027607
|
G | T | 1 | a0005c0005t0001g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4149-2288G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027607 | ||||||
| chr7:92027616
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4149-2279T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027616 | ||||||
| chr7:92027643
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4149-2252C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027643 | ||||||
| chr7:92027732
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4149-2163G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027732 | ||||||
| chr7:92027798
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4149-2097C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027798 | ||||||
| chr7:92027802
|
A | G | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4149-2093A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92027802 | ||||||
| chr7:92028113
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4149-1782C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028113 | ||||||
| chr7:92028295
|
TA | T | 11 | a0001c0001t0001g0096a0001c0001t0001g0157a0001c0001t0001g0158others(8): Show | 11 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.4149-1572delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92028295 | |||||
| chr7:92028295
|
TAA | T | 65 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0050others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.4149-1573_4149-157 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92028295 | |||||
| chr7:92028295
|
TAAA | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(204): Show |
intron_variant | MODIFIER | c.4149-1574_4149-157 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92028295 | |||||
| chr7:92028295
|
TAAAA | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0086others(10): Show | 13 | HG02083.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4149-1575_4149-157 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92028295 | |||||
| chr7:92028326
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4149-1569A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028326 | ||||||
| chr7:92028358
|
G | A | 15 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0222others(12): Show | 15 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.4149-1537G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028358 | ||||||
| chr7:92028378
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4149-1517C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028378 | ||||||
| chr7:92028466
|
A | G | 1 | a0011c0029t0002g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4149-1429A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028466 | ||||||
| chr7:92028603
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4149-1292G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028603 | ||||||
| chr7:92028639
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4149-1256A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028639 | ||||||
| chr7:92028680
|
A | G | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4149-1215A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028680 | ||||||
| chr7:92028687
|
G | A | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4149-1208G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92028687 | ||||||
| chr7:92029119
|
C | CT | 7 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0002g0245others(4): Show | 7 | HG00639.hp2 HG02145.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4149-766dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92029119 | |||||
| chr7:92029139
|
C | G | 10 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0133others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4149-756C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029139 | ||||||
| chr7:92029194
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4149-701A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029194 | ||||||
| chr7:92029227
|
TACAG | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.4149-666_4149-663d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | INFO_REALIGN_3_PRIME | chr7 | 92029227 | |||||
| chr7:92029306
|
C | T | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.4149-589C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029306 | ||||||
| chr7:92029351
|
C | T | 2 | a0002c0002t0002g0270a0002c0002t0002g0271 | 2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.4149-544C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029351 | ||||||
| chr7:92029366
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4149-529G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029366 | ||||||
| chr7:92029634
|
A | G | 1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4149-261A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029634 | ||||||
| chr7:92029836
|
C | G | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4149-59C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029836 | ||||||
| chr7:92029846
|
A | G | 1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4149-49A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 14/49 | chr7 | 92029846 | ||||||
| chr7:92030207
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4245+216T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030207 | ||||||
| chr7:92030640
|
C | CA | 28 | a0001c0001t0001g0045a0001c0001t0001g0115a0001c0001t0001g0116others(25): Show | 28 | HG00423.hp2 HG00639.hp2 HG01978.hp1 others(25): Show |
intron_variant | MODIFIER | c.4245+666dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | INFO_REALIGN_3_PRIME | chr7 | 92030640 | |||||
| chr7:92030640
|
CA | C | 14 | a0003c0003t0002g0296a0004c0004t0001g0192a0004c0004t0001g0193others(11): Show | 14 | HG00639.hp1 HG01884.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.4245+666delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | INFO_REALIGN_3_PRIME | chr7 | 92030640 | |||||
| chr7:92030730
|
G | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4245+739G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030730 | ||||||
| chr7:92030739
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4245+748A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030739 | ||||||
| chr7:92030809
|
GTAT | G | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.4246-698_4246-696d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | INFO_REALIGN_3_PRIME | chr7 | 92030809 | |||||
| chr7:92030840
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0041 | 2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.4246-672T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030840 | ||||||
| chr7:92030911
|
G | T | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.4246-601G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030911 | ||||||
| chr7:92030931
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4246-581C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030931 | ||||||
| chr7:92030932
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4246-580G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030932 | ||||||
| chr7:92030975
|
G | C | 1 | a0002c0002t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4246-537G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92030975 | ||||||
| chr7:92031061
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4246-451G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92031061 | ||||||
| chr7:92031132
|
A | T | 1 | a0001c0001t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4246-380A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92031132 | ||||||
| chr7:92031167
|
C | T | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4246-345C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92031167 | ||||||
| chr7:92031335
|
G | T | 1 | a0002c0002t0002g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4246-177G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 15/49 | chr7 | 92031335 | ||||||
| chr7:92031797
|
G | C | 99 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(96): Show | 99 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.4338+193G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92031797 | ||||||
| chr7:92032423
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4338+819G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92032423 | ||||||
| chr7:92032496
|
C | CA | 11 | a0001c0001t0001g0030a0002c0002t0002g0242a0002c0002t0002g0243others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.4338+909dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92032496 | |||||
| chr7:92032496
|
CA | C | 65 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0080others(62): Show | 65 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.4338+909delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92032496 | |||||
| chr7:92032537
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4338+933G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92032537 | ||||||
| chr7:92032715
|
A | G | 6 | a0002c0002t0002g0279a0002c0002t0002g0280a0002c0002t0002g0282others(3): Show | 6 | HG00642.hp1 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.4338+1111A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92032715 | ||||||
| chr7:92032760
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(29): Show | 32 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.4338+1156T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92032760 | ||||||
| chr7:92032914
|
C | A | 1 | a0001c0011t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4338+1310C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92032914 | ||||||
| chr7:92033208
|
A | T | 1 | a0002c0002t0002g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4338+1604A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033208 | ||||||
| chr7:92033237
|
A | C | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.4338+1633A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033237 | ||||||
| chr7:92033250
|
A | T | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4338+1646A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033250 | ||||||
| chr7:92033298
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4338+1694G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033298 | ||||||
| chr7:92033330
|
A | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4338+1726A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033330 | ||||||
| chr7:92033363
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4338+1759C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033363 | ||||||
| chr7:92033399
|
T | C | 1 | a0001c0011t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4338+1795T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033399 | ||||||
| chr7:92033442
|
C | CT | 21 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0062others(18): Show | 21 | HG01192.hp1 HG02074.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.4338+1859dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92033442 | |||||
| chr7:92033442
|
CT | C | 87 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0083others(84): Show | 87 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.4338+1859delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92033442 | |||||
| chr7:92033442
|
CTT | C | 16 | a0002c0002t0002g0269a0002c0033t0002g0275a0004c0004t0001g0192others(13): Show | 16 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4338+1858_4338+185 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92033442 | |||||
| chr7:92033447
|
T | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4338+1843T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033447 | ||||||
| chr7:92033448
|
T | C | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4338+1844T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033448 | ||||||
| chr7:92033536
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4338+1932C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033536 | ||||||
| chr7:92033898
|
G | A | 2 | a0005c0005t0001g0154a0005c0005t0001g0155 | 2 | NA18747.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.4338+2294G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033898 | ||||||
| chr7:92033952
|
C | T | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4338+2348C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033952 | ||||||
| chr7:92033981
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4338+2377G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92033981 | ||||||
| chr7:92034050
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4338+2446A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034050 | ||||||
| chr7:92034215
|
A | G | 75 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(72): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.4338+2611A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034215 | ||||||
| chr7:92034259
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4338+2655G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034259 | ||||||
| chr7:92034272
|
G | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4338+2668G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034272 | ||||||
| chr7:92034439
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4338+2835G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034439 | ||||||
| chr7:92034480
|
C | CTA | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0019others(60): Show | 63 | HG00280.hp2 HG00558.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.4338+2894_4338+289 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034480 | |||||
| chr7:92034484
|
A | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4338+2880A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034484 | ||||||
| chr7:92034496
|
A | AT | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(41): Show | 44 | HG00280.hp1 HG00597.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.4338+2893dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034496 | |||||
| chr7:92034496
|
A | ATT | 3 | a0001c0001t0001g0096a0001c0001t0001g0142a0001c0008t0001g0189 | 3 | HG03516.hp1 NA18940.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.4338+2893_4338+289 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034496 | |||||
| chr7:92034496
|
A | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0158 | 2 | HG02976.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4338+2892A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034496 | ||||||
| chr7:92034498
|
A | AT | 33 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(30): Show | 33 | HG00738.hp2 HG01070.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.4338+2915dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034498 | |||||
| chr7:92034498
|
A | ATT | 11 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0092others(8): Show | 11 | HG00558.hp1 HG01981.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.4338+2914_4338+291 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034498 | |||||
| chr7:92034498
|
A | T | 55 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 55 | HG00280.hp1 HG00597.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.4338+2894A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034498 | ||||||
| chr7:92034498
|
AT | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(10): Show | 13 | HG00621.hp2 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4338+2915delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034498 | |||||
| chr7:92034498
|
ATTT | A | 14 | a0003c0003t0002g0212a0004c0004t0001g0192a0004c0004t0001g0193others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.4338+2913_4338+291 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92034498 | |||||
| chr7:92034499
|
T | TA | 16 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 16 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.4338+2895_4338+289 others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034499 | ||||||
| chr7:92034500
|
T | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.4338+2896T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034500 | ||||||
| chr7:92034501
|
T | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(14): Show | 17 | HG01074.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.4338+2897T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034501 | ||||||
| chr7:92034502
|
T | A | 84 | a0001c0001t0001g0050a0002c0002t0002g0213a0002c0002t0002g0214others(81): Show | 84 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.4338+2898T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034502 | ||||||
| chr7:92034503
|
T | A | 5 | a0001c0001t0001g0047a0001c0011t0001g0011a0002c0002t0002g0244others(2): Show | 5 | HG01361.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4338+2899T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034503 | ||||||
| chr7:92034504
|
T | A | 64 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0216others(61): Show | 64 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.4338+2900T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034504 | ||||||
| chr7:92034505
|
T | A | 1 | a0001c0011t0001g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4338+2901T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034505 | ||||||
| chr7:92034506
|
T | A | 18 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0222others(15): Show | 18 | HG01074.hp2 HG01975.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.4338+2902T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034506 | ||||||
| chr7:92034508
|
T | A | 2 | a0002c0002t0002g0226a0002c0002t0002g0232 | 2 | HG02300.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4338+2904T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034508 | ||||||
| chr7:92034581
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0167a0001c0001t0001g0187others(1): Show | 4 | HG00597.hp1 NA18955.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.4338+2977A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034581 | ||||||
| chr7:92034758
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4338+3154C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034758 | ||||||
| chr7:92034808
|
C | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4338+3204C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92034808 | ||||||
| chr7:92035314
|
G | C | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4339-3105G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035314 | ||||||
| chr7:92035331
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4339-3088A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035331 | ||||||
| chr7:92035625
|
T | TA | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4339-2787dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | INFO_REALIGN_3_PRIME | chr7 | 92035625 | |||||
| chr7:92035765
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4339-2654A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035765 | ||||||
| chr7:92035794
|
G | A | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4339-2625G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035794 | ||||||
| chr7:92035808
|
G | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4339-2611G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035808 | ||||||
| chr7:92035931
|
G | A | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4339-2488G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92035931 | ||||||
| chr7:92036039
|
T | A | 1 | a0024c0017t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4339-2380T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036039 | ||||||
| chr7:92036312
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4339-2107T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036312 | ||||||
| chr7:92036313
|
A | T | 115 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(112): Show | 115 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.4339-2106A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036313 | ||||||
| chr7:92036318
|
T | G | 1 | a0002c0002t0002g0267 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4339-2101T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036318 | ||||||
| chr7:92036393
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4339-2026C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036393 | ||||||
| chr7:92036723
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4339-1696G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92036723 | ||||||
| chr7:92037010
|
A | T | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4339-1409A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037010 | ||||||
| chr7:92037055
|
C | T | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4339-1364C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037055 | ||||||
| chr7:92037232
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4339-1187T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037232 | ||||||
| chr7:92037347
|
A | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.4339-1072A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037347 | ||||||
| chr7:92037449
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0170 | 2 | HG02074.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.4339-970T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037449 | ||||||
| chr7:92037458
|
C | A | 1 | a0002c0002t0002g0263 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4339-961C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037458 | ||||||
| chr7:92037913
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4339-506T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92037913 | ||||||
| chr7:92038012
|
G | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4339-407G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92038012 | ||||||
| chr7:92038100
|
T | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4339-319T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92038100 | ||||||
| chr7:92038327
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4339-92C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92038327 | ||||||
| chr7:92038378
|
T | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4339-41T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 16/49 | chr7 | 92038378 | ||||||
| chr7:92038901
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | NA18952.hp2 NA18953.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.4692+129G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92038901 | ||||||
| chr7:92039051
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4692+279G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92039051 | ||||||
| chr7:92039540
|
C | T | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.4692+768C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92039540 | ||||||
| chr7:92039595
|
T | A | 26 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(23): Show | 26 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.4692+823T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92039595 | ||||||
| chr7:92039868
|
G | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4693-806G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92039868 | ||||||
| chr7:92040021
|
G | T | 1 | a0013c0031t0002g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4693-653G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040021 | ||||||
| chr7:92040082
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4693-592A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040082 | ||||||
| chr7:92040494
|
G | A | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.4693-180G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040494 | ||||||
| chr7:92040634
|
TA | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4693-39delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040634 | ||||||
| chr7:92040636
|
T | C | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4693-38T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040636 | ||||||
| chr7:92040644
|
T | G | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4693-30T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | chr7 | 92040644 | ||||||
| chr7:92040646
|
G | GT | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.4693-11dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | INFO_REALIGN_3_PRIME | chr7 | 92040646 | |||||
| chr7:92040646
|
G | GTT | 10 | a0001c0001t0001g0030a0001c0001t0001g0058a0002c0002t0002g0220others(7): Show | 10 | HG01346.hp2 HG01978.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.4693-12_4693-11dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 17/49 | INFO_REALIGN_3_PRIME | chr7 | 92040646 | |||||
| chr7:92041004
|
A | AT | 97 | a0001c0001t0001g0002a0001c0022t0001g0126a0002c0002t0002g0213others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.4917+121dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | INFO_REALIGN_3_PRIME | chr7 | 92041004 | |||||
| chr7:92041388
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4917+490A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041388 | ||||||
| chr7:92041538
|
A | C | 6 | a0002c0002t0002g0219a0002c0002t0002g0222a0002c0002t0002g0233others(3): Show | 6 | HG02071.hp2 NA18956.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.4918-508A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041538 | ||||||
| chr7:92041636
|
C | T | 1 | a0017c0025t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4918-410C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041636 | ||||||
| chr7:92041684
|
T | C | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.4918-362T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041684 | ||||||
| chr7:92041691
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4918-355A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041691 | ||||||
| chr7:92041693
|
A | G | 96 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.4918-353A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041693 | ||||||
| chr7:92041706
|
A | G | 117 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(114): Show | 117 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.4918-340A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041706 | ||||||
| chr7:92041960
|
C | T | 1 | a0004c0004t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4918-86C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 18/49 | chr7 | 92041960 | ||||||
| chr7:92042539
|
C | A | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.5059-129C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 19/49 | chr7 | 92042539 | ||||||
| chr7:92042831
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5162+60T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92042831 | ||||||
| chr7:92042843
|
T | A | 1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5162+72T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92042843 | ||||||
| chr7:92042852
|
T | C | 2 | a0005c0005t0001g0129a0024c0017t0001g0149 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.5162+81T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92042852 | ||||||
| chr7:92042855
|
T | C | 1 | a0006c0006t0001g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5162+84T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92042855 | ||||||
| chr7:92043089
|
G | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5162+318G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043089 | ||||||
| chr7:92043131
|
A | T | 1 | a0001c0001t0001g0004 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.5162+360A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043131 | ||||||
| chr7:92043132
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5162+361C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043132 | ||||||
| chr7:92043400
|
G | A | 1 | a0002c0002t0002g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5162+629G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043400 | ||||||
| chr7:92043498
|
G | GT | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5162+728dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | INFO_REALIGN_3_PRIME | chr7 | 92043498 | |||||
| chr7:92043693
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5162+922A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043693 | ||||||
| chr7:92043731
|
G | A | 3 | a0002c0002t0002g0254a0002c0002t0002g0256a0002c0002t0002g0260 | 3 | NA19064.hp1 NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.5162+960G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043731 | ||||||
| chr7:92043994
|
A | T | 95 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(92): Show | 95 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.5163-1014A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92043994 | ||||||
| chr7:92044095
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5163-913G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044095 | ||||||
| chr7:92044125
|
G | A | 1 | a0002c0002t0002g0249 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5163-883G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044125 | ||||||
| chr7:92044217
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0032others(6): Show | 9 | HG00558.hp2 HG02083.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.5163-791A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044217 | ||||||
| chr7:92044280
|
C | A | 4 | a0002c0002t0002g0267a0002c0002t0002g0268a0002c0002t0002g0305others(1): Show | 4 | HG00735.hp1 HG01192.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5163-728C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044280 | ||||||
| chr7:92044309
|
C | T | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.5163-699C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044309 | ||||||
| chr7:92044322
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5163-686T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044322 | ||||||
| chr7:92044467
|
T | C | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5163-541T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044467 | ||||||
| chr7:92044580
|
A | G | 1 | a0002c0002t0002g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5163-428A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044580 | ||||||
| chr7:92044876
|
G | GTAT | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 194 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(191): Show |
intron_variant | MODIFIER | c.5163-130_5163-128d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | INFO_REALIGN_3_PRIME | chr7 | 92044876 | |||||
| chr7:92044988
|
G | A | 118 | a0001c0001t0001g0130a0001c0022t0001g0126a0002c0002t0002g0213others(115): Show | 118 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.5163-20G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 20/49 | chr7 | 92044988 | ||||||
| chr7:92045493
|
T | C | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.5368+280T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92045493 | ||||||
| chr7:92045565
|
G | C | 1 | a0002c0002t0002g0256 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5368+352G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92045565 | ||||||
| chr7:92045693
|
T | G | 22 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0096others(19): Show | 22 | HG00597.hp1 HG02523.hp1 NA18747.hp1 others(19): Show |
intron_variant | MODIFIER | c.5368+480T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92045693 | ||||||
| chr7:92045830
|
C | CT | 52 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0050others(49): Show | 52 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.5368+638dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92045830 | |||||
| chr7:92045981
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5368+768A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92045981 | ||||||
| chr7:92046685
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5368+1472G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92046685 | ||||||
| chr7:92046832
|
C | G | 2 | a0005c0005t0001g0154a0005c0005t0001g0155 | 2 | NA18747.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.5368+1619C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92046832 | ||||||
| chr7:92046929
|
G | A | 1 | a0007c0007t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5368+1716G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92046929 | ||||||
| chr7:92047410
|
G | A | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.5368+2197G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92047410 | ||||||
| chr7:92047498
|
C | T | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5368+2285C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92047498 | ||||||
| chr7:92047657
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5368+2444T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92047657 | ||||||
| chr7:92047806
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5368+2593G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92047806 | ||||||
| chr7:92047859
|
A | G | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5368+2646A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92047859 | ||||||
| chr7:92048342
|
A | G | 2 | a0001c0001t0001g0042a0001c0018t0001g0010 | 2 | NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5368+3129A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92048342 | ||||||
| chr7:92048368
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0135 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5368+3155C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92048368 | ||||||
| chr7:92048887
|
T | C | 1 | a0002c0002t0002g0285 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5368+3674T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92048887 | ||||||
| chr7:92049201
|
T | A | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5369-3525T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049201 | ||||||
| chr7:92049212
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0041 | 2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.5369-3514C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049212 | ||||||
| chr7:92049276
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5369-3450A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049276 | ||||||
| chr7:92049376
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5369-3350C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049376 | ||||||
| chr7:92049414
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.5369-3312G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049414 | ||||||
| chr7:92049542
|
C | T | 4 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5369-3184C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049542 | ||||||
| chr7:92049603
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5369-3123T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049603 | ||||||
| chr7:92049612
|
A | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5369-3114A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049612 | ||||||
| chr7:92049702
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5369-3024T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049702 | ||||||
| chr7:92049719
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0151a0021c0020t0001g0141 | 3 | HG01106.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.5369-3007A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049719 | ||||||
| chr7:92049765
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0044 | 2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.5369-2961G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049765 | ||||||
| chr7:92049857
|
G | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.5369-2869G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049857 | ||||||
| chr7:92049936
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5369-2790A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049936 | ||||||
| chr7:92049984
|
G | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5369-2742G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92049984 | ||||||
| chr7:92050063
|
C | CT | 10 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0104others(7): Show | 10 | HG01361.hp2 HG02027.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.5369-2644dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92050063 | |||||
| chr7:92050063
|
CT | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0117a0002c0002t0002g0251others(38): Show | 41 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5369-2644delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92050063 | |||||
| chr7:92050205
|
C | CA | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.5369-2520dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92050205 | |||||
| chr7:92050223
|
G | C | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.5369-2503G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92050223 | ||||||
| chr7:92050270
|
A | G | 1 | a0003c0003t0002g0295 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5369-2456A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92050270 | ||||||
| chr7:92050573
|
T | C | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5369-2153T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92050573 | ||||||
| chr7:92050829
|
A | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5369-1897A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92050829 | ||||||
| chr7:92050922
|
ACGCATAT others(3): Show |
A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5369-1802_5369-179 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92050922 | |||||
| chr7:92050964
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5369-1762C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92050964 | ||||||
| chr7:92051215
|
T | A | 26 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(23): Show | 26 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.5369-1511T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051215 | ||||||
| chr7:92051327
|
G | A | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.5369-1399G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051327 | ||||||
| chr7:92051341
|
T | C | 75 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(72): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.5369-1385T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051341 | ||||||
| chr7:92051572
|
A | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0071others(1): Show | 4 | HG00597.hp2 NA18970.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.5369-1154A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051572 | ||||||
| chr7:92051660
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 266 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(263): Show |
intron_variant | MODIFIER | c.5369-1066G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051660 | ||||||
| chr7:92051789
|
G | A | 5 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(2): Show | 5 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.5369-937G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92051789 | ||||||
| chr7:92052248
|
C | T | 2 | a0006c0006t0001g0203a0006c0006t0001g0204 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5369-478C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92052248 | ||||||
| chr7:92052283
|
CA | C | 117 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(114): Show | 117 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.5369-441delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92052283 | |||||
| chr7:92052307
|
A | G | 1 | a0003c0003t0002g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5369-419A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92052307 | ||||||
| chr7:92052475
|
G | GA | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.5369-244dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | INFO_REALIGN_3_PRIME | chr7 | 92052475 | |||||
| chr7:92052606
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5369-120T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 21/49 | chr7 | 92052606 | ||||||
| chr7:92053059
|
T | C | 1 | a0002c0002t0002g0277 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5601+101T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92053059 | ||||||
| chr7:92053156
|
G | A | 2 | a0001c0001t0001g0028a0016c0028t0001g0003 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.5601+198G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92053156 | ||||||
| chr7:92053534
|
T | C | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.5601+576T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92053534 | ||||||
| chr7:92053585
|
G | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.5601+627G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92053585 | ||||||
| chr7:92053659
|
G | A | 1 | a0002c0002t0002g0238 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5601+701G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92053659 | ||||||
| chr7:92054406
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5601+1448A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92054406 | ||||||
| chr7:92054535
|
G | C | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.5601+1577G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92054535 | ||||||
| chr7:92054772
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.5601+1814A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92054772 | ||||||
| chr7:92055379
|
G | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5601+2421G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92055379 | ||||||
| chr7:92055627
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5601+2669G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92055627 | ||||||
| chr7:92055639
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5601+2681G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92055639 | ||||||
| chr7:92055663
|
T | C | 1 | a0005c0005t0001g0147 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5601+2705T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92055663 | ||||||
| chr7:92055988
|
A | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0139 | 3 | NA18973.hp1 NA19070.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.5601+3030A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92055988 | ||||||
| chr7:92056071
|
ATTAATAT | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5601+3121_5601+312 others(11): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | INFO_REALIGN_3_PRIME | chr7 | 92056071 | |||||
| chr7:92056260
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5601+3302A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92056260 | ||||||
| chr7:92056286
|
G | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5601+3328G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92056286 | ||||||
| chr7:92057057
|
TA | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0018t0001g0010 | 3 | NA18974.hp1 NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5601+4102delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | INFO_REALIGN_3_PRIME | chr7 | 92057057 | |||||
| chr7:92057243
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5602-4017G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92057243 | ||||||
| chr7:92057475
|
A | G | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.5602-3785A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92057475 | ||||||
| chr7:92058037
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5602-3223A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058037 | ||||||
| chr7:92058169
|
A | G | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5602-3091A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058169 | ||||||
| chr7:92058182
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0120 | 3 | HG02027.hp2 HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.5602-3078G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058182 | ||||||
| chr7:92058188
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5602-3072A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058188 | ||||||
| chr7:92058371
|
T | G | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5602-2889T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058371 | ||||||
| chr7:92058390
|
T | C | 1 | a0023c0024t0001g0160 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5602-2870T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058390 | ||||||
| chr7:92058545
|
G | A | 1 | a0002c0002t0002g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5602-2715G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058545 | ||||||
| chr7:92058631
|
G | T | 1 | a0002c0002t0002g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5602-2629G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058631 | ||||||
| chr7:92058759
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5602-2501C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92058759 | ||||||
| chr7:92059156
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5602-2104A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92059156 | ||||||
| chr7:92059713
|
C | CAT | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5602-1547_5602-154 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92059713 | ||||||
| chr7:92060037
|
C | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.5602-1223C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060037 | ||||||
| chr7:92060132
|
T | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5602-1128T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060132 | ||||||
| chr7:92060147
|
G | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5602-1113G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060147 | ||||||
| chr7:92060219
|
T | G | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5602-1041T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060219 | ||||||
| chr7:92060477
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5602-783G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060477 | ||||||
| chr7:92060821
|
A | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5602-439A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060821 | ||||||
| chr7:92060988
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5602-272T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92060988 | ||||||
| chr7:92061143
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5602-117A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 22/49 | chr7 | 92061143 | ||||||
| chr7:92061584
|
C | CTA | 24 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0097others(21): Show | 24 | HG00621.hp1 HG02155.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.5764+197_5764+198d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATA | 24 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0057others(21): Show | 24 | HG00423.hp2 HG01070.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.5764+195_5764+198d others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATA | 17 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0088others(14): Show | 17 | HG00738.hp2 HG01123.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.5764+193_5764+198d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(1): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0094others(5): Show | 8 | HG00558.hp1 HG01109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.5764+191_5764+198d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(3): Show |
8 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0047others(5): Show | 8 | HG00621.hp2 HG01358.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.5764+189_5764+198d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(5): Show |
10 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0105others(7): Show | 10 | HG02486.hp2 HG02523.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.5764+187_5764+198d others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(7): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0028others(7): Show | 10 | HG02129.hp2 HG03209.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.5764+185_5764+198d others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(9): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0036others(4): Show | 7 | HG02630.hp1 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5764+183_5764+198d others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(11): Show |
20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG00280.hp1 HG00423.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.5764+181_5764+198d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(13): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0025others(12): Show | 15 | HG00639.hp1 HG00673.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.5764+179_5764+198d others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(15): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0052others(3): Show | 6 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.5764+177_5764+198d others(24): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(17): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0136 | 2 | HG01081.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.5764+175_5764+198d others(26): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(19): Show |
2 | a0001c0001t0001g0023a0006c0006t0001g0203 | 2 | HG01884.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.5764+173_5764+198d others(28): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
C | CTATATAT others(27): Show |
1 | a0006c0006t0001g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5764+165_5764+198d others(36): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTA | C | 11 | a0001c0001t0001g0183a0002c0002t0002g0213a0002c0002t0002g0214others(8): Show | 11 | HG00642.hp2 HG00673.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.5764+197_5764+198d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTATATA | C | 20 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 20 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.5764+193_5764+198d others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTATATAT others(1): Show |
C | 71 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(68): Show | 71 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.5764+191_5764+198d others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTATATAT others(3): Show |
C | 4 | a0001c0001t0001g0055a0003c0003t0002g0212a0003c0003t0002g0240others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.5764+189_5764+198d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTATATAT others(9): Show |
C | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0071others(2): Show | 5 | HG00597.hp2 NA18970.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.5764+183_5764+198d others(18): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061584
|
CTATATAT others(11): Show |
C | 1 | a0026c0015t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5764+181_5764+198d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | INFO_REALIGN_3_PRIME | chr7 | 92061584 | |||||
| chr7:92061620
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0021a0015c0032t0002g0239 | 2 | HG02559.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.5764+198_5764+199i others(17): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061620 | ||||||
| chr7:92061620
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0058 | 2 | NA18957.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.5764+198_5764+199i others(27): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061620 | ||||||
| chr7:92061621
|
A | T | 13 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(10): Show | 13 | HG01884.hp1 HG02647.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.5764+199A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061621 | ||||||
| chr7:92061622
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0138a0005c0005t0001g0148 | 3 | HG02129.hp1 HG02723.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.5764+200A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061622 | ||||||
| chr7:92061624
|
T | TA | 3 | a0001c0001t0001g0090a0001c0001t0001g0138a0005c0005t0001g0148 | 3 | HG02129.hp1 HG02723.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.5764+202_5764+203i others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061624 | ||||||
| chr7:92061632
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5764+210A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061632 | ||||||
| chr7:92061756
|
G | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 266 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(263): Show |
intron_variant | MODIFIER | c.5764+334G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061756 | ||||||
| chr7:92061893
|
A | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG00738.hp2 HG01256.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.5765-381A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061893 | ||||||
| chr7:92061971
|
T | C | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.5765-303T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 23/49 | chr7 | 92061971 | ||||||
| chr7:92062531
|
T | C | 1 | a0009c0012t0002g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5977+45T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92062531 | ||||||
| chr7:92062632
|
G | T | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5977+146G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92062632 | ||||||
| chr7:92062712
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5977+226A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92062712 | ||||||
| chr7:92062971
|
A | G | 1 | a0005c0005t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5977+485A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92062971 | ||||||
| chr7:92063060
|
T | C | 1 | a0003c0003t0002g0293 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5977+574T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92063060 | ||||||
| chr7:92063086
|
T | TA | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.5977+602dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92063086 | |||||
| chr7:92063348
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5977+862A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92063348 | ||||||
| chr7:92063432
|
C | CT | 30 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.5977+961dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92063432 | |||||
| chr7:92063432
|
CTT | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5977+960_5977+961d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92063432 | |||||
| chr7:92063446
|
T | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5977+960T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92063446 | ||||||
| chr7:92063890
|
T | C | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5978-1341T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92063890 | ||||||
| chr7:92064159
|
A | T | 1 | a0002c0002t0002g0237 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.5978-1072A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064159 | ||||||
| chr7:92064340
|
C | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0016c0028t0001g0003 | 3 | HG02523.hp2 NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.5978-891C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064340 | ||||||
| chr7:92064465
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0072 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.5978-766T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064465 | ||||||
| chr7:92064523
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.5978-708A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064523 | ||||||
| chr7:92064586
|
G | GGCCTACG others(342): Show |
1 | a0001c0001t0001g0137 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.5978-628_5978-627i others(351): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92064586 | |||||
| chr7:92064586
|
G | GGCCTACG others(353): Show |
1 | a0001c0001t0001g0131 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5978-628_5978-627i others(362): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92064586 | |||||
| chr7:92064767
|
T | C | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.5978-464T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064767 | ||||||
| chr7:92064804
|
T | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.5978-427T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92064804 | ||||||
| chr7:92064936
|
A | AT | 6 | a0001c0001t0001g0064a0001c0001t0001g0079a0001c0001t0001g0099others(3): Show | 6 | HG03453.hp1 HG03834.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.5978-283dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | INFO_REALIGN_3_PRIME | chr7 | 92064936 | |||||
| chr7:92065185
|
A | T | 6 | a0002c0002t0002g0219a0002c0002t0002g0222a0002c0002t0002g0233others(3): Show | 6 | HG02071.hp2 NA18956.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.5978-46A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 24/49 | chr7 | 92065185 | ||||||
| chr7:92065587
|
C | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18952.hp2 NA18953.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.6210+124C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 25/49 | chr7 | 92065587 | ||||||
| chr7:92066248
|
A | C | 1 | a0028c0014t0002g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6211-179A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 25/49 | chr7 | 92066248 | ||||||
| chr7:92066383
|
A | G | 1 | a0002c0002t0002g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6211-44A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 25/49 | chr7 | 92066383 | ||||||
| chr7:92066403
|
A | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6211-24A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 25/49 | chr7 | 92066403 | ||||||
| chr7:92066894
|
C | T | 3 | a0002c0002t0002g0280a0002c0002t0002g0284a0002c0002t0002g0285 | 3 | HG01516.hp1 HG03492.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6330+348C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92066894 | ||||||
| chr7:92067066
|
C | G | 1 | a0002c0002t0002g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6330+520C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067066 | ||||||
| chr7:92067127
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.6330+581A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067127 | ||||||
| chr7:92067154
|
T | C | 1 | a0002c0002t0002g0224 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.6330+608T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067154 | ||||||
| chr7:92067282
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0184 | 2 | HG01109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.6330+736A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067282 | ||||||
| chr7:92067405
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.6330+859G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067405 | ||||||
| chr7:92067455
|
C | CCT | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6330+910_6330+911d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | INFO_REALIGN_3_PRIME | chr7 | 92067455 | |||||
| chr7:92067681
|
A | G | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6330+1135A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067681 | ||||||
| chr7:92067853
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6330+1307A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067853 | ||||||
| chr7:92067997
|
G | A | 1 | a0003c0003t0002g0293 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6330+1451G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92067997 | ||||||
| chr7:92068054
|
T | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6330+1508T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068054 | ||||||
| chr7:92068143
|
G | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6330+1597G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068143 | ||||||
| chr7:92068218
|
T | C | 1 | a0002c0002t0002g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6330+1672T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068218 | ||||||
| chr7:92068365
|
C | CA | 23 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0163others(20): Show | 23 | HG01123.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.6331-1643dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | INFO_REALIGN_3_PRIME | chr7 | 92068365 | |||||
| chr7:92068365
|
CA | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG01168.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6331-1643delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | INFO_REALIGN_3_PRIME | chr7 | 92068365 | |||||
| chr7:92068378
|
A | G | 5 | a0002c0002t0002g0221a0002c0002t0002g0225a0002c0002t0002g0230others(2): Show | 5 | NA18991.hp2 NA18992.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.6331-1652A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068378 | ||||||
| chr7:92068384
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6331-1646A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068384 | ||||||
| chr7:92068462
|
G | A | 1 | a0026c0015t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6331-1568G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068462 | ||||||
| chr7:92068975
|
C | G | 2 | a0003c0003t0002g0291a0003c0003t0002g0301 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6331-1055C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92068975 | ||||||
| chr7:92069021
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6331-1009G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069021 | ||||||
| chr7:92069345
|
G | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6331-685G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069345 | ||||||
| chr7:92069401
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6331-629A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069401 | ||||||
| chr7:92069518
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6331-512A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069518 | ||||||
| chr7:92069987
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.6331-43T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069987 | ||||||
| chr7:92069989
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.6331-41A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92069989 | ||||||
| chr7:92070022
|
T | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.6331-8T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 26/49 | chr7 | 92070022 | ||||||
| chr7:92070233
|
A | C | 4 | a0002c0002t0002g0244a0002c0002t0002g0245a0002c0002t0002g0248others(1): Show | 4 | HG00639.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.6507+27A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070233 | ||||||
| chr7:92070398
|
GTTGTTGT others(11): Show |
G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6507+198_6507+215d others(20): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070398 | |||||
| chr7:92070401
|
G | GTTGTT | 18 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0096others(15): Show | 18 | HG03239.hp1 HG04228.hp1 HG04228.hp2 others(15): Show |
intron_variant | MODIFIER | c.6507+238_6507+242d others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070401 | |||||
| chr7:92070401
|
GTTGTT | G | 25 | a0001c0001t0001g0008a0001c0001t0001g0074a0001c0001t0001g0082others(22): Show | 25 | HG00738.hp1 HG01070.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.6507+238_6507+242d others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070401 | |||||
| chr7:92070401
|
GTTGTTTT others(3): Show |
G | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 150 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.6507+233_6507+242d others(12): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070401 | |||||
| chr7:92070401
|
GTTGTTTT others(8): Show |
G | 4 | a0001c0001t0001g0012a0008c0009t0002g0207a0008c0009t0002g0209others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6507+228_6507+242d others(17): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070401 | |||||
| chr7:92070401
|
GTTGTTTT others(13): Show |
G | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.6507+223_6507+242d others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070401 | |||||
| chr7:92070465
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6507+259G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070465 | ||||||
| chr7:92070491
|
A | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG00738.hp2 HG01256.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.6507+285A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070491 | ||||||
| chr7:92070593
|
A | C | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.6508-312A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070593 | ||||||
| chr7:92070666
|
C | T | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6508-239C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070666 | ||||||
| chr7:92070676
|
C | A | 1 | a0002c0002t0002g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6508-229C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070676 | ||||||
| chr7:92070806
|
C | CA | 267 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.6508-80dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070806 | |||||
| chr7:92070806
|
C | CAA | 9 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0163others(6): Show | 9 | HG01106.hp2 HG02976.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.6508-81_6508-80dup others(2): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | INFO_REALIGN_3_PRIME | chr7 | 92070806 | |||||
| chr7:92070849
|
C | T | 1 | a0005c0005t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6508-56C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 27/49 | chr7 | 92070849 | ||||||
| chr7:92071137
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0114others(1): Show | 4 | HG00423.hp2 NA18945.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.6612+128A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071137 | ||||||
| chr7:92071244
|
A | G | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6612+235A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071244 | ||||||
| chr7:92071305
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6612+296T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071305 | ||||||
| chr7:92071327
|
AAT | A | 116 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(113): Show | 116 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.6612+323_6612+324d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92071327 | |||||
| chr7:92071388
|
G | T | 2 | a0003c0003t0002g0296a0022c0021t0001g0166 | 2 | HG02523.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6612+379G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071388 | ||||||
| chr7:92071388
|
GT | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.6612+393delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92071388 | |||||
| chr7:92071513
|
T | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6612+504T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071513 | ||||||
| chr7:92071565
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.6612+556A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92071565 | ||||||
| chr7:92071971
|
A | AT | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6612+970dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92071971 | |||||
| chr7:92072032
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6612+1023G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072032 | ||||||
| chr7:92072034
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6612+1025G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072034 | ||||||
| chr7:92072085
|
C | T | 1 | a0006c0006t0001g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6612+1076C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072085 | ||||||
| chr7:92072320
|
G | T | 5 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(2): Show | 5 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.6612+1311G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072320 | ||||||
| chr7:92072516
|
AGTATAAA others(2934): Show |
A | 1 | a0001c0001t0001g0019 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6612+1510_6613-139 others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92072516 | |||||
| chr7:92072554
|
G | T | 10 | a0005c0005t0001g0127a0005c0005t0001g0128a0005c0005t0001g0129others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.6612+1545G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072554 | ||||||
| chr7:92072809
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6612+1800A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072809 | ||||||
| chr7:92072829
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6612+1820G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072829 | ||||||
| chr7:92072960
|
G | A | 1 | a0013c0031t0002g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6612+1951G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92072960 | ||||||
| chr7:92073006
|
T | C | 3 | a0002c0002t0003g0258a0002c0002t0003g0261a0002c0002t0003g0266 | 3 | HG00280.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.6612+1997T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073006 | ||||||
| chr7:92073086
|
C | T | 1 | a0002c0002t0002g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6612+2077C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073086 | ||||||
| chr7:92073129
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6612+2120C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073129 | ||||||
| chr7:92073149
|
A | G | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.6612+2140A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073149 | ||||||
| chr7:92073286
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6612+2277G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073286 | ||||||
| chr7:92073326
|
C | T | 1 | a0002c0002t0002g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6612+2317C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073326 | ||||||
| chr7:92073340
|
C | CA | 112 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0124others(109): Show | 112 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.6612+2347dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92073340 | |||||
| chr7:92073383
|
G | A | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6612+2374G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073383 | ||||||
| chr7:92073426
|
A | C | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.6612+2417A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073426 | ||||||
| chr7:92073483
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6612+2474G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073483 | ||||||
| chr7:92073532
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6612+2523G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92073532 | ||||||
| chr7:92074021
|
G | A | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6613-2834G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074021 | ||||||
| chr7:92074114
|
CTATCCAT others(15): Show |
C | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6613-2734_6613-271 others(26): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92074114 | |||||
| chr7:92074154
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6613-2701G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074154 | ||||||
| chr7:92074258
|
C | T | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6613-2597C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074258 | ||||||
| chr7:92074396
|
A | G | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6613-2459A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074396 | ||||||
| chr7:92074402
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.6613-2453A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074402 | ||||||
| chr7:92074453
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6613-2402G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074453 | ||||||
| chr7:92074454
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6613-2401C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074454 | ||||||
| chr7:92074545
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6613-2310A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074545 | ||||||
| chr7:92074621
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.6613-2234A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074621 | ||||||
| chr7:92074699
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6613-2156C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074699 | ||||||
| chr7:92074719
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.6613-2136G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074719 | ||||||
| chr7:92074847
|
A | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6613-2008A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92074847 | ||||||
| chr7:92075090
|
T | TA | 10 | a0005c0005t0001g0127a0005c0005t0001g0128a0005c0005t0001g0129others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.6613-1755dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92075090 | |||||
| chr7:92075090
|
TA | T | 96 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6613-1755delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | INFO_REALIGN_3_PRIME | chr7 | 92075090 | |||||
| chr7:92075178
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.6613-1677C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075178 | ||||||
| chr7:92075225
|
T | G | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6613-1630T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075225 | ||||||
| chr7:92075579
|
G | T | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.6613-1276G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075579 | ||||||
| chr7:92075645
|
G | A | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6613-1210G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075645 | ||||||
| chr7:92075689
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18970.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.6613-1166T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075689 | ||||||
| chr7:92075960
|
G | A | 75 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(72): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.6613-895G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92075960 | ||||||
| chr7:92076115
|
C | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6613-740C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92076115 | ||||||
| chr7:92076290
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6613-565A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92076290 | ||||||
| chr7:92076382
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.6613-473A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92076382 | ||||||
| chr7:92076391
|
C | G | 17 | a0001c0001t0001g0130a0004c0004t0001g0192a0004c0004t0001g0193others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.6613-464C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92076391 | ||||||
| chr7:92076731
|
C | G | 4 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6613-124C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 28/49 | chr7 | 92076731 | ||||||
| chr7:92077067
|
T | TTTA | 94 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(91): Show | 94 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.6765+81_6765+83dup others(3): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | INFO_REALIGN_3_PRIME | chr7 | 92077067 | |||||
| chr7:92077091
|
T | C | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.6765+84T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077091 | ||||||
| chr7:92077092
|
C | CT | 85 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0216others(82): Show | 85 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.6765+88dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | INFO_REALIGN_3_PRIME | chr7 | 92077092 | |||||
| chr7:92077092
|
C | T | 3 | a0002c0002t0002g0215a0002c0002t0002g0228a0002c0002t0002g0281 | 3 | HG01928.hp2 HG02622.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.6765+85C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077092 | ||||||
| chr7:92077096
|
C | T | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6765+89C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077096 | ||||||
| chr7:92077175
|
A | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6765+168A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077175 | ||||||
| chr7:92077217
|
C | T | 1 | a0002c0002t0002g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6765+210C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077217 | ||||||
| chr7:92077250
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6765+243G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077250 | ||||||
| chr7:92077310
|
C | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6765+303C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077310 | ||||||
| chr7:92077312
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0055others(1): Show | 4 | NA18977.hp1 NA18981.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.6765+305C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 29/49 | chr7 | 92077312 | ||||||
| chr7:92077883
|
C | T | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
splice_region_variant&intron_variant | LOW | c.6945+8C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92077883 | ||||||
| chr7:92078054
|
T | A | 1 | a0002c0002t0002g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6945+179T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078054 | ||||||
| chr7:92078122
|
G | A | 1 | a0005c0005t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6945+247G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078122 | ||||||
| chr7:92078290
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.6945+415G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078290 | ||||||
| chr7:92078306
|
T | TTTTAA | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6945+435_6945+436i others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | INFO_REALIGN_3_PRIME | chr7 | 92078306 | |||||
| chr7:92078466
|
A | G | 96 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.6945+591A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078466 | ||||||
| chr7:92078538
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6946-541C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078538 | ||||||
| chr7:92078607
|
T | C | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.6946-472T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078607 | ||||||
| chr7:92078644
|
T | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.6946-435T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078644 | ||||||
| chr7:92078793
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6946-286G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078793 | ||||||
| chr7:92078905
|
T | C | 40 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0253others(37): Show | 40 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.6946-174T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 30/49 | chr7 | 92078905 | ||||||
| chr7:92080195
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.8019+43A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080195 | ||||||
| chr7:92080262
|
T | G | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8019+110T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080262 | ||||||
| chr7:92080319
|
A | G | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.8019+167A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080319 | ||||||
| chr7:92080414
|
C | T | 2 | a0002c0002t0002g0305a0002c0002t0002g0306 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.8019+262C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080414 | ||||||
| chr7:92080455
|
G | C | 6 | a0002c0002t0002g0221a0002c0002t0002g0224a0002c0002t0002g0225others(3): Show | 6 | NA18991.hp2 NA18992.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.8019+303G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080455 | ||||||
| chr7:92080491
|
G | A | 1 | a0026c0015t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8019+339G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080491 | ||||||
| chr7:92080543
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.8019+391A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080543 | ||||||
| chr7:92080599
|
CA | C | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.8019+459delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92080599 | |||||
| chr7:92080609
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.8019+457A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080609 | ||||||
| chr7:92080637
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8019+485A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080637 | ||||||
| chr7:92080724
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.8019+572A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92080724 | ||||||
| chr7:92081018
|
A | C | 10 | a0005c0005t0001g0127a0005c0005t0001g0128a0005c0005t0001g0129others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.8019+866A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081018 | ||||||
| chr7:92081028
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8019+876A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081028 | ||||||
| chr7:92081152
|
G | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 194 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(191): Show |
intron_variant | MODIFIER | c.8019+1000G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081152 | ||||||
| chr7:92081199
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.8019+1047G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081199 | ||||||
| chr7:92081335
|
G | T | 1 | a0004c0004t0001g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8019+1183G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081335 | ||||||
| chr7:92081343
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.8020-1179G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081343 | ||||||
| chr7:92081452
|
G | A | 1 | a0002c0002t0002g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8020-1070G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081452 | ||||||
| chr7:92081473
|
TTA | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 176 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.8020-1025_8020-102 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081473 | |||||
| chr7:92081489
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.8020-1033A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081489 | ||||||
| chr7:92081493
|
A | AT | 4 | a0002c0002t0002g0285a0003c0003t0002g0212a0003c0003t0002g0295others(1): Show | 4 | HG01516.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.8020-1028dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081493 | |||||
| chr7:92081493
|
A | ATT | 49 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0002g0244others(46): Show | 49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.8020-1028_8020-102 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081493 | |||||
| chr7:92081493
|
A | T | 10 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0291others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.8020-1029A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081493 | ||||||
| chr7:92081494
|
TA | T | 14 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(11): Show | 14 | HG00639.hp1 HG01243.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.8020-1027delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081494 | ||||||
| chr7:92081495
|
A | ATT | 13 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(10): Show | 13 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.8020-1026_8020-102 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081495 | |||||
| chr7:92081495
|
A | ATTT | 7 | a0002c0002t0002g0219a0002c0002t0002g0222a0002c0002t0002g0233others(4): Show | 7 | HG02071.hp2 HG03669.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.8020-1026_8020-102 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081495 | |||||
| chr7:92081495
|
A | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0048a0002c0002t0002g0242others(65): Show | 68 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.8020-1027A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081495 | ||||||
| chr7:92081497
|
A | ATTTT | 8 | a0002c0002t0002g0220a0002c0002t0002g0223a0002c0002t0002g0226others(5): Show | 8 | HG01928.hp2 HG01975.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.8020-1015_8020-101 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | INFO_REALIGN_3_PRIME | chr7 | 92081497 | |||||
| chr7:92081497
|
A | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 185 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(182): Show |
intron_variant | MODIFIER | c.8020-1025A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081497 | ||||||
| chr7:92081498
|
T | TATA | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.8020-1024_8020-102 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081498 | ||||||
| chr7:92081499
|
T | A | 1 | a0005c0005t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.8020-1023T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081499 | ||||||
| chr7:92081522
|
G | A | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.8020-1000G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081522 | ||||||
| chr7:92081531
|
A | G | 117 | a0001c0001t0001g0130a0002c0002t0002g0213a0002c0002t0002g0214others(114): Show | 117 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.8020-991A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081531 | ||||||
| chr7:92081915
|
T | C | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.8020-607T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92081915 | ||||||
| chr7:92082152
|
C | T | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.8020-370C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92082152 | ||||||
| chr7:92082224
|
C | T | 2 | a0004c0004t0001g0194a0026c0015t0001g0001 | 2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.8020-298C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92082224 | ||||||
| chr7:92082477
|
A | G | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.8020-45A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 31/49 | chr7 | 92082477 | ||||||
| chr7:92082839
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.8160+177T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 32/49 | chr7 | 92082839 | ||||||
| chr7:92083027
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8161-143C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 32/49 | chr7 | 92083027 | ||||||
| chr7:92083164
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.8161-6T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 32/49 | chr7 | 92083164 | ||||||
| chr7:92083702
|
TA | T | 97 | a0001c0001t0001g0027a0001c0001t0001g0088a0001c0001t0001g0145others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.8646+59delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | INFO_REALIGN_3_PRIME | chr7 | 92083702 | |||||
| chr7:92083703
|
A | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8646+48A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083703 | ||||||
| chr7:92083704
|
A | T | 93 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(90): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.8646+49A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083704 | ||||||
| chr7:92083705
|
A | T | 1 | a0002c0002t0002g0265 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8646+50A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083705 | ||||||
| chr7:92083733
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.8646+78T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083733 | ||||||
| chr7:92083786
|
T | G | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.8646+131T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083786 | ||||||
| chr7:92083903
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8646+248G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083903 | ||||||
| chr7:92083935
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18942.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.8646+280G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92083935 | ||||||
| chr7:92084103
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0011t0001g0011others(3): Show | 6 | HG02258.hp2 HG03486.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.8646+448C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92084103 | ||||||
| chr7:92084399
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.8647-241T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92084399 | ||||||
| chr7:92084560
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.8647-80G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92084560 | ||||||
| chr7:92084566
|
C | G | 9 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0002g0244others(6): Show | 9 | HG00639.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.8647-74C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 33/49 | chr7 | 92084566 | ||||||
| chr7:92084811
|
T | C | 1 | a0004c0004t0001g0205 | 1 | HG02896.hp2 | splice_region_variant&intron_variant | LOW | c.8711-8T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 34/49 | chr7 | 92084811 | ||||||
| chr7:92085347
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.8833-148C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 35/49 | chr7 | 92085347 | ||||||
| chr7:92085480
|
G | A | 1 | a0002c0002t0002g0260 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.8833-15G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 35/49 | chr7 | 92085480 | ||||||
| chr7:92085819
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9024+133C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 36/49 | chr7 | 92085819 | ||||||
| chr7:92085998
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.9025-230G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 36/49 | chr7 | 92085998 | ||||||
| chr7:92086479
|
G | C | 1 | a0002c0002t0002g0298 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.9213+63G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92086479 | ||||||
| chr7:92086723
|
G | C | 1 | a0005c0005t0001g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.9213+307G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92086723 | ||||||
| chr7:92086766
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.9213+350C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92086766 | ||||||
| chr7:92086790
|
G | A | 100 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(97): Show | 100 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.9213+374G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92086790 | ||||||
| chr7:92087030
|
G | T | 21 | a0002c0002t0002g0219a0002c0002t0002g0220a0002c0002t0002g0221others(18): Show | 21 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.9213+614G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087030 | ||||||
| chr7:92087149
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9213+733A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087149 | ||||||
| chr7:92087214
|
A | G | 1 | a0004c0004t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.9213+798A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087214 | ||||||
| chr7:92087249
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9213+833G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087249 | ||||||
| chr7:92087637
|
T | C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.9213+1221T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087637 | ||||||
| chr7:92087656
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.9213+1240G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087656 | ||||||
| chr7:92087890
|
T | A | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.9213+1474T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92087890 | ||||||
| chr7:92088023
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.9214-1362A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088023 | ||||||
| chr7:92088084
|
A | G | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9214-1301A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088084 | ||||||
| chr7:92088176
|
C | G | 84 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(81): Show | 84 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.9214-1209C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088176 | ||||||
| chr7:92088242
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0167a0001c0001t0001g0187others(1): Show | 4 | HG00597.hp1 NA18955.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.9214-1143C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088242 | ||||||
| chr7:92088392
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.9214-993T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088392 | ||||||
| chr7:92088657
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.9214-728G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088657 | ||||||
| chr7:92088692
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.9214-693G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92088692 | ||||||
| chr7:92089032
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9214-353A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92089032 | ||||||
| chr7:92089150
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.9214-235G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92089150 | ||||||
| chr7:92089317
|
T | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9214-68T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92089317 | ||||||
| chr7:92089318
|
T | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9214-67T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 37/49 | chr7 | 92089318 | ||||||
| chr7:92089539
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.9358+10A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089539 | ||||||
| chr7:92089546
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.9358+17G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089546 | ||||||
| chr7:92089560
|
A | G | 1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9358+31A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089560 | ||||||
| chr7:92089620
|
T | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9358+91T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089620 | ||||||
| chr7:92089692
|
A | G | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9358+163A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089692 | ||||||
| chr7:92089721
|
A | T | 1 | a0021c0020t0001g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.9358+192A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089721 | ||||||
| chr7:92089822
|
T | C | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9358+293T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089822 | ||||||
| chr7:92089854
|
G | A | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.9358+325G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92089854 | ||||||
| chr7:92090149
|
T | G | 9 | a0001c0022t0001g0126a0003c0003t0002g0288a0003c0003t0002g0289others(6): Show | 9 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.9358+620T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090149 | ||||||
| chr7:92090198
|
A | G | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9358+669A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090198 | ||||||
| chr7:92090294
|
C | T | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9358+765C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090294 | ||||||
| chr7:92090439
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9358+910A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090439 | ||||||
| chr7:92090491
|
C | T | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9358+962C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090491 | ||||||
| chr7:92090621
|
C | CA | 9 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0130others(6): Show | 9 | HG02109.hp1 HG02922.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.9358+1112dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92090621 | |||||
| chr7:92090621
|
CAAAAAAA others(2): Show |
C | 96 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.9358+1104_9358+111 others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92090621 | |||||
| chr7:92090638
|
AAAAG | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01081.hp1 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.9358+1112_9358+111 others(8): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92090638 | |||||
| chr7:92090914
|
G | A | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.9358+1385G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92090914 | ||||||
| chr7:92091201
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0120 | 3 | HG02027.hp2 HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.9358+1672G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091201 | ||||||
| chr7:92091352
|
C | A | 6 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0105others(3): Show | 6 | HG00558.hp1 NA18939.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.9359-1745C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091352 | ||||||
| chr7:92091402
|
A | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9359-1695A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091402 | ||||||
| chr7:92091559
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.9359-1538T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091559 | ||||||
| chr7:92091565
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9359-1532G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091565 | ||||||
| chr7:92091585
|
C | CA | 27 | a0001c0022t0001g0126a0002c0002t0002g0244a0002c0002t0002g0245others(24): Show | 27 | HG00639.hp1 HG00673.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.9359-1500dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92091585 | |||||
| chr7:92091597
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 185 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.9359-1500A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091597 | ||||||
| chr7:92091597
|
AC | A | 3 | a0002c0002t0002g0230a0002c0002t0002g0298a0003c0003t0002g0296 | 3 | HG03453.hp1 NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.9359-1499delC | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091597 | ||||||
| chr7:92091598
|
C | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(296): Show | 299 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.9359-1499C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091598 | ||||||
| chr7:92091600
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.9359-1497A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091600 | ||||||
| chr7:92091603
|
A | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9359-1494A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091603 | ||||||
| chr7:92091615
|
G | C | 2 | a0005c0005t0001g0152a0005c0005t0001g0153 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.9359-1482G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091615 | ||||||
| chr7:92091617
|
A | T | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.9359-1480A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091617 | ||||||
| chr7:92091662
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.9359-1435G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091662 | ||||||
| chr7:92091770
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.9359-1327G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091770 | ||||||
| chr7:92091801
|
C | T | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9359-1296C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92091801 | ||||||
| chr7:92091888
|
TTA | T | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.9359-1207_9359-120 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92091888 | |||||
| chr7:92092098
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.9359-999C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092098 | ||||||
| chr7:92092194
|
A | G | 1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9359-903A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092194 | ||||||
| chr7:92092215
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.9359-882T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092215 | ||||||
| chr7:92092267
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9359-830A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092267 | ||||||
| chr7:92092348
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9359-749A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092348 | ||||||
| chr7:92092355
|
G | A | 3 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210 | 3 | HG02280.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.9359-742G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092355 | ||||||
| chr7:92092359
|
G | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.9359-738G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092359 | ||||||
| chr7:92092507
|
GT | G | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.9359-579delT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | INFO_REALIGN_3_PRIME | chr7 | 92092507 | |||||
| chr7:92092532
|
G | C | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.9359-565G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 38/49 | chr7 | 92092532 | ||||||
| chr7:92093629
|
T | C | 2 | a0001c0001t0001g0028a0016c0028t0001g0003 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.9578+313T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92093629 | ||||||
| chr7:92093652
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9578+336A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92093652 | ||||||
| chr7:92093758
|
T | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9578+442T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92093758 | ||||||
| chr7:92093889
|
C | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9578+573C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92093889 | ||||||
| chr7:92094118
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.9578+802C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094118 | ||||||
| chr7:92094205
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.9579-818A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094205 | ||||||
| chr7:92094377
|
C | T | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.9579-646C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094377 | ||||||
| chr7:92094390
|
G | A | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9579-633G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094390 | ||||||
| chr7:92094563
|
G | A | 1 | a0001c0011t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9579-460G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094563 | ||||||
| chr7:92094610
|
G | A | 1 | a0002c0002t0002g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.9579-413G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 39/49 | chr7 | 92094610 | ||||||
| chr7:92095439
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0184 | 2 | HG01109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.9729+266G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095439 | ||||||
| chr7:92095577
|
C | T | 1 | a0003c0003t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.9729+404C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095577 | ||||||
| chr7:92095595
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9729+422C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095595 | ||||||
| chr7:92095722
|
C | T | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.9729+549C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095722 | ||||||
| chr7:92095818
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.9729+645T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095818 | ||||||
| chr7:92095943
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9730-746C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92095943 | ||||||
| chr7:92096040
|
C | T | 1 | a0002c0002t0002g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.9730-649C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096040 | ||||||
| chr7:92096334
|
G | GT | 54 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(51): Show | 54 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.9730-338dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | INFO_REALIGN_3_PRIME | chr7 | 92096334 | |||||
| chr7:92096334
|
G | GTT | 14 | a0001c0008t0001g0189a0004c0004t0001g0192a0004c0004t0001g0193others(11): Show | 14 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.9730-339_9730-338d others(4): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | INFO_REALIGN_3_PRIME | chr7 | 92096334 | |||||
| chr7:92096339
|
T | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02155.hp2 NA19001.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.9730-350T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096339 | ||||||
| chr7:92096340
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.9730-349T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096340 | ||||||
| chr7:92096380
|
G | C | 6 | a0002c0002t0002g0279a0002c0002t0002g0280a0002c0002t0002g0282others(3): Show | 6 | HG00642.hp1 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.9730-309G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096380 | ||||||
| chr7:92096426
|
C | A | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9730-263C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096426 | ||||||
| chr7:92096581
|
C | G | 1 | a0025c0026t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9730-108C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096581 | ||||||
| chr7:92096588
|
C | G | 1 | a0001c0022t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9730-101C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096588 | ||||||
| chr7:92096617
|
G | A | 1 | a0022c0021t0001g0166 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.9730-72G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 40/49 | chr7 | 92096617 | ||||||
| chr7:92097549
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.10399-37A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 41/49 | chr7 | 92097549 | ||||||
| chr7:92097903
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.10607+109T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/49 | chr7 | 92097903 | ||||||
| chr7:92098031
|
G | A | 1 | a0002c0002t0002g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.10608-78G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/49 | chr7 | 92098031 | ||||||
| chr7:92098071
|
G | A | 96 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.10608-38G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/49 | chr7 | 92098071 | ||||||
| chr7:92098094
|
G | C | 4 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.10608-15G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 42/49 | chr7 | 92098094 | ||||||
| chr7:92098373
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10713+159C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92098373 | ||||||
| chr7:92098408
|
G | T | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10713+194G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92098408 | ||||||
| chr7:92098543
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02155.hp2 NA19001.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.10713+329C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92098543 | ||||||
| chr7:92098749
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.10713+535A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92098749 | ||||||
| chr7:92099210
|
G | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(5): Show | 8 | HG00423.hp1 HG02129.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.10714-477G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92099210 | ||||||
| chr7:92099609
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.10714-78C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 43/49 | chr7 | 92099609 | ||||||
| chr7:92100058
|
G | GGAAACCA others(5): Show |
1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.10896+191_10896+20 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/49 | INFO_REALIGN_3_PRIME | chr7 | 92100058 | |||||
| chr7:92100241
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.10896+372T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/49 | chr7 | 92100241 | ||||||
| chr7:92100497
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.10897-359A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/49 | chr7 | 92100497 | ||||||
| chr7:92100813
|
C | G | 1 | a0004c0004t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.10897-43C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/49 | chr7 | 92100813 | ||||||
| chr7:92100832
|
G | T | 1 | a0011c0029t0002g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.10897-24G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 44/49 | chr7 | 92100832 | ||||||
| chr7:92101277
|
A | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0176 | 2 | HG01358.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.11097+221A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101277 | ||||||
| chr7:92101351
|
C | T | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.11097+295C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101351 | ||||||
| chr7:92101426
|
G | A | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11097+370G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101426 | ||||||
| chr7:92101427
|
A | G | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11097+371A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101427 | ||||||
| chr7:92101436
|
C | CA | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(30): Show | 33 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.11097+396dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92101436 | |||||
| chr7:92101436
|
CA | C | 98 | a0001c0001t0001g0107a0001c0022t0001g0126a0002c0002t0002g0213others(95): Show | 98 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.11097+396delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92101436 | |||||
| chr7:92101436
|
CAA | C | 16 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0194others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.11097+395_11097+39 others(6): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92101436 | |||||
| chr7:92101536
|
C | T | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.11097+480C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101536 | ||||||
| chr7:92101732
|
C | T | 2 | a0005c0005t0001g0152a0005c0005t0001g0153 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.11097+676C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101732 | ||||||
| chr7:92101733
|
G | A | 101 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(98): Show | 101 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.11097+677G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101733 | ||||||
| chr7:92101762
|
A | G | 1 | a0002c0002t0002g0267 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.11097+706A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92101762 | ||||||
| chr7:92102088
|
G | A | 79 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(76): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.11098-506G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102088 | ||||||
| chr7:92102161
|
T | TAAAAA | 30 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0254others(27): Show | 30 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.11098-433_11098-43 others(9): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102161 | ||||||
| chr7:92102161
|
TTTA | T | 31 | a0001c0022t0001g0126a0002c0002t0002g0219a0002c0002t0002g0220others(28): Show | 31 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.11098-432_11098-43 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102161 | ||||||
| chr7:92102162
|
T | A | 38 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(35): Show | 38 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.11098-432T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102162 | ||||||
| chr7:92102163
|
T | A | 69 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(66): Show | 69 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.11098-431T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102163 | ||||||
| chr7:92102163
|
T | TA | 13 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.11098-421dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102163 | |||||
| chr7:92102166
|
A | AT | 38 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(35): Show | 38 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.11098-428_11098-42 others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102166 | ||||||
| chr7:92102166
|
A | T | 31 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0254others(28): Show | 31 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.11098-428A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102166 | ||||||
| chr7:92102167
|
AAAAAAAT others(4): Show |
A | 16 | a0001c0001t0001g0020a0004c0004t0001g0192a0004c0004t0001g0193others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.11098-423_11098-41 others(15): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102167 | |||||
| chr7:92102170
|
A | AT | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.11098-424_11098-42 others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102170 | ||||||
| chr7:92102170
|
A | ATAAAT | 3 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0035 | 3 | HG02040.hp1 HG02071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.11098-424_11098-42 others(9): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102170 | ||||||
| chr7:92102170
|
A | T | 104 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0185others(101): Show | 104 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.11098-424A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102170 | ||||||
| chr7:92102174
|
T | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(58): Show | 61 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.11098-420T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102174 | ||||||
| chr7:92102178
|
T | A | 4 | a0001c0001t0001g0081a0001c0011t0001g0011a0005c0005t0001g0147others(1): Show | 4 | HG01516.hp2 HG02129.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.11098-416T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102178 | ||||||
| chr7:92102192
|
AATAAATA others(5): Show |
A | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.11098-398_11098-38 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102192 | |||||
| chr7:92102200
|
A | G | 3 | a0001c0001t0001g0058a0005c0005t0001g0129a0024c0017t0001g0149 | 3 | HG00735.hp2 HG03239.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.11098-394A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102200 | ||||||
| chr7:92102204
|
G | A | 117 | a0001c0001t0001g0043a0001c0022t0001g0126a0002c0002t0002g0213others(114): Show | 117 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.11098-390G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102204 | ||||||
| chr7:92102254
|
T | G | 3 | a0003c0003t0002g0289a0003c0003t0002g0292a0003c0003t0002g0293 | 3 | HG02717.hp1 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.11098-340T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102254 | ||||||
| chr7:92102448
|
T | TTAC | 7 | a0001c0001t0001g0029a0001c0001t0001g0158a0007c0007t0002g0302others(4): Show | 7 | HG02523.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.11098-106_11098-10 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
T | TTACTAC | 6 | a0001c0001t0001g0134a0001c0001t0001g0180a0001c0022t0001g0126others(3): Show | 6 | HG02280.hp1 HG02922.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.11098-109_11098-10 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
T | TTACTACT others(2): Show |
23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0088others(20): Show | 23 | HG00423.hp2 HG00738.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.11098-112_11098-10 others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
T | TTACTACT others(5): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0046others(12): Show | 15 | HG00621.hp1 HG00673.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.11098-115_11098-10 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
T | TTACTACT others(8): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0113 | 3 | NA18942.hp1 NA18949.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.11098-118_11098-10 others(19): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
T | TTACTACT others(11): Show |
1 | a0001c0001t0001g0110 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.11098-121_11098-10 others(22): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
TTAC | T | 14 | a0001c0001t0001g0041a0001c0001t0001g0140a0001c0001t0001g0143others(11): Show | 14 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.11098-106_11098-10 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
TTACTAC | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 157 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.11098-109_11098-10 others(10): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
TTACTACT others(2): Show |
T | 5 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0051others(2): Show | 5 | HG02027.hp1 HG03492.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.11098-112_11098-10 others(13): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102448
|
TTACTACT others(5): Show |
T | 1 | a0001c0001t0001g0109 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.11098-115_11098-10 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102448 | |||||
| chr7:92102481
|
C | G | 1 | a0003c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.11098-113C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102481 | ||||||
| chr7:92102488
|
T | TACC | 6 | a0003c0003t0002g0212a0003c0003t0002g0295a0007c0007t0002g0302others(3): Show | 6 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.11098-91_11098-89d others(5): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102488 | |||||
| chr7:92102488
|
T | TACTACTA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.11098-104_11098-10 others(16): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | INFO_REALIGN_3_PRIME | chr7 | 92102488 | |||||
| chr7:92102510
|
T | A | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11098-84T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102510 | ||||||
| chr7:92102511
|
G | C | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11098-83G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102511 | ||||||
| chr7:92102514
|
A | T | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11098-80A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102514 | ||||||
| chr7:92102545
|
G | A | 1 | a0002c0002t0002g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.11098-49G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 45/49 | chr7 | 92102545 | ||||||
| chr7:92103094
|
T | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.11330+268T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103094 | ||||||
| chr7:92103387
|
C | CA | 70 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(67): Show | 70 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.11330+587dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | INFO_REALIGN_3_PRIME | chr7 | 92103387 | |||||
| chr7:92103387
|
CA | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(77): Show | 80 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.11330+587delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | INFO_REALIGN_3_PRIME | chr7 | 92103387 | |||||
| chr7:92103387
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0002g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11330+577_11330+58 others(15): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | INFO_REALIGN_3_PRIME | chr7 | 92103387 | |||||
| chr7:92103413
|
A | G | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11330+587A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103413 | ||||||
| chr7:92103476
|
G | A | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.11330+650G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103476 | ||||||
| chr7:92103562
|
G | A | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11330+736G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103562 | ||||||
| chr7:92103563
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18940.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.11330+737C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103563 | ||||||
| chr7:92103577
|
C | A | 2 | a0009c0012t0002g0217a0009c0012t0002g0218 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.11330+751C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103577 | ||||||
| chr7:92103613
|
T | C | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11330+787T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103613 | ||||||
| chr7:92103651
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.11330+825C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103651 | ||||||
| chr7:92103670
|
C | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 195 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.11330+844C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103670 | ||||||
| chr7:92103694
|
C | CA | 15 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0097others(12): Show | 15 | HG01981.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.11330+884dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | INFO_REALIGN_3_PRIME | chr7 | 92103694 | |||||
| chr7:92103729
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.11330+903C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103729 | ||||||
| chr7:92103846
|
G | C | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11330+1020G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92103846 | ||||||
| chr7:92104061
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.11330+1235G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104061 | ||||||
| chr7:92104155
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.11330+1329C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104155 | ||||||
| chr7:92104190
|
A | AT | 18 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0053others(15): Show | 18 | HG00738.hp1 HG01361.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.11330+1382dupT | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | INFO_REALIGN_3_PRIME | chr7 | 92104190 | |||||
| chr7:92104190
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0094 | 2 | HG00558.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.11330+1364A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104190 | ||||||
| chr7:92104193
|
T | TA | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.11330+1367_11330+1 others(7): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104193 | ||||||
| chr7:92104194
|
T | A | 48 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0080others(45): Show | 48 | HG00597.hp1 HG00642.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.11330+1368T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104194 | ||||||
| chr7:92104197
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.11330+1371T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104197 | ||||||
| chr7:92104198
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.11330+1372T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104198 | ||||||
| chr7:92104201
|
T | A | 11 | a0001c0001t0001g0130a0004c0004t0001g0194a0007c0007t0002g0287others(8): Show | 11 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.11330+1375T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104201 | ||||||
| chr7:92104205
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.11330+1379T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104205 | ||||||
| chr7:92104230
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.11330+1404G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104230 | ||||||
| chr7:92104340
|
A | G | 1 | a0005c0005t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.11331-1338A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104340 | ||||||
| chr7:92104351
|
C | T | 75 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(72): Show | 75 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.11331-1327C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104351 | ||||||
| chr7:92104515
|
G | A | 49 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0002g0244others(46): Show | 49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.11331-1163G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104515 | ||||||
| chr7:92104621
|
G | T | 1 | a0002c0033t0002g0275 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.11331-1057G>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104621 | ||||||
| chr7:92104648
|
A | C | 1 | a0014c0013t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11331-1030A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104648 | ||||||
| chr7:92104891
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.11331-787A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92104891 | ||||||
| chr7:92105062
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.11331-616C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105062 | ||||||
| chr7:92105092
|
A | G | 1 | a0022c0021t0001g0166 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.11331-586A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105092 | ||||||
| chr7:92105148
|
T | C | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.11331-530T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105148 | ||||||
| chr7:92105223
|
C | G | 3 | a0007c0007t0002g0302a0007c0007t0002g0303a0007c0007t0002g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.11331-455C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105223 | ||||||
| chr7:92105238
|
T | C | 118 | a0001c0001t0001g0130a0001c0022t0001g0126a0002c0002t0002g0213others(115): Show | 118 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.11331-440T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105238 | ||||||
| chr7:92105503
|
A | G | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11331-175A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105503 | ||||||
| chr7:92105560
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.11331-118A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105560 | ||||||
| chr7:92105617
|
T | C | 4 | a0008c0009t0002g0207a0008c0009t0002g0209a0008c0009t0002g0210others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.11331-61T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105617 | ||||||
| chr7:92105667
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11331-11A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 46/49 | chr7 | 92105667 | ||||||
| chr7:92105793
|
T | A | 5 | a0004c0004t0001g0194a0007c0007t0002g0287a0007c0007t0002g0302others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.11416+30T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92105793 | ||||||
| chr7:92105872
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.11416+109G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92105872 | ||||||
| chr7:92105985
|
A | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.11416+222A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92105985 | ||||||
| chr7:92106299
|
T | A | 102 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(99): Show | 102 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.11416+536T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106299 | ||||||
| chr7:92106371
|
GA | G | 96 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(93): Show | 96 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.11416+613delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | INFO_REALIGN_3_PRIME | chr7 | 92106371 | |||||
| chr7:92106418
|
AGTAGGGA others(3): Show |
A | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.11416+657_11416+66 others(14): Show |
AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | INFO_REALIGN_3_PRIME | chr7 | 92106418 | |||||
| chr7:92106434
|
A | C | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.11416+671A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106434 | ||||||
| chr7:92106682
|
A | G | 2 | a0005c0005t0001g0152a0005c0005t0001g0153 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.11417-611A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106682 | ||||||
| chr7:92106764
|
A | C | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.11417-529A>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106764 | ||||||
| chr7:92106784
|
C | G | 102 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(99): Show | 102 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.11417-509C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106784 | ||||||
| chr7:92106819
|
A | T | 1 | a0015c0032t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.11417-474A>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106819 | ||||||
| chr7:92106952
|
A | G | 3 | a0003c0003t0002g0212a0003c0003t0002g0295a0028c0014t0002g0208 | 3 | HG02451.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.11417-341A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106952 | ||||||
| chr7:92106982
|
C | T | 4 | a0007c0007t0002g0287a0007c0007t0002g0302a0007c0007t0002g0303others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.11417-311C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106982 | ||||||
| chr7:92106992
|
C | G | 8 | a0003c0003t0002g0288a0003c0003t0002g0289a0003c0003t0002g0290others(5): Show | 8 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.11417-301C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92106992 | ||||||
| chr7:92107120
|
G | A | 1 | a0004c0004t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.11417-173G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92107120 | ||||||
| chr7:92107150
|
T | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.11417-143T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92107150 | ||||||
| chr7:92107158
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.11417-135A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 47/49 | chr7 | 92107158 | ||||||
| chr7:92107480
|
T | A | 118 | a0001c0001t0001g0130a0001c0022t0001g0126a0002c0002t0002g0213others(115): Show | 118 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.11546+58T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107480 | ||||||
| chr7:92107488
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.11546+66C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107488 | ||||||
| chr7:92107560
|
A | G | 117 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(114): Show | 117 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.11546+138A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107560 | ||||||
| chr7:92107575
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18952.hp2 NA18953.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.11546+153A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107575 | ||||||
| chr7:92107607
|
C | T | 98 | a0001c0001t0001g0017a0001c0022t0001g0126a0002c0002t0002g0213others(95): Show | 98 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.11546+185C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107607 | ||||||
| chr7:92107608
|
G | A | 15 | a0004c0004t0001g0192a0004c0004t0001g0193a0004c0004t0001g0196others(12): Show | 15 | HG00639.hp1 HG01884.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.11546+186G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107608 | ||||||
| chr7:92107743
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 195 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.11546+321T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107743 | ||||||
| chr7:92107807
|
T | C | 102 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(99): Show | 102 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.11546+385T>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107807 | ||||||
| chr7:92107833
|
G | A | 1 | a0002c0002t0002g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.11546+411G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107833 | ||||||
| chr7:92107911
|
C | T | 1 | a0004c0004t0001g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11546+489C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107911 | ||||||
| chr7:92107912
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 194 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(191): Show |
intron_variant | MODIFIER | c.11546+490A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107912 | ||||||
| chr7:92107982
|
G | A | 2 | a0004c0004t0001g0205a0004c0004t0001g0206 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.11547-512G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92107982 | ||||||
| chr7:92108010
|
T | G | 97 | a0001c0022t0001g0126a0002c0002t0002g0213a0002c0002t0002g0214others(94): Show | 97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.11547-484T>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92108010 | ||||||
| chr7:92108019
|
CA | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(246): Show | 249 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.11547-460delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | INFO_REALIGN_3_PRIME | chr7 | 92108019 | |||||
| chr7:92108034
|
A | G | 1 | a0001c0011t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11547-460A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92108034 | ||||||
| chr7:92108035
|
G | A | 1 | a0001c0011t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11547-459G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 48/49 | chr7 | 92108035 | ||||||
| chr7:92109049
|
G | GA | 7 | a0001c0011t0001g0013a0004c0004t0001g0194a0007c0007t0002g0287others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.11686+432dupA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | INFO_REALIGN_3_PRIME | chr7 | 92109049 | |||||
| chr7:92109049
|
GA | G | 80 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(77): Show | 80 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.11686+432delA | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | INFO_REALIGN_3_PRIME | chr7 | 92109049 | |||||
| chr7:92109123
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.11686+490A>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109123 | ||||||
| chr7:92109272
|
G | C | 5 | a0004c0004t0001g0194a0007c0007t0002g0287a0007c0007t0002g0302others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.11686+639G>C | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109272 | ||||||
| chr7:92109323
|
T | A | 1 | a0001c0018t0001g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11686+690T>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109323 | ||||||
| chr7:92109474
|
C | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.11687-648C>G | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109474 | ||||||
| chr7:92109481
|
C | A | 1 | a0002c0002t0002g0285 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.11687-641C>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109481 | ||||||
| chr7:92109883
|
G | A | 3 | a0002c0002t0002g0273a0002c0002t0002g0274a0002c0002t0002g0276 | 3 | HG01256.hp1 HG01261.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.11687-239G>A | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109883 | ||||||
| chr7:92109923
|
C | T | 2 | a0001c0001t0001g0064a0017c0025t0001g0063 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.11687-199C>T | AKAP9 | ENSG00000127914.19 | transcript | ENST00000356239.8 | protein_coding | 49/49 | chr7 | 92109923 |