| geneid | 107 |
|---|---|
| ensemblid | ENSG00000164742.16 |
| hgncid | 232 |
| symbol | ADCY1 |
| name | adenylate cyclase 1 |
| refseq_nuc | NM_021116.4 |
| refseq_prot | NP_066939.1 |
| ensembl_nuc | ENST00000297323.12 |
| ensembl_prot | ENSP00000297323.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 45574368 |
| end | 45723116 |
| strand | + |
| ver | v1.2 |
| region | chr7:45574368-45723116 |
| region5000 | chr7:45569368-45728116 |
| regionname0 | ADCY1_chr7_45574368_45723116 |
| regionname5000 | ADCY1_chr7_45569368_45728116 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1119 | 266 | 70 | 47 | 115 | 8 | 24 | 85 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0002 | 0/0 | 1119 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0003 | 0/0 | 1123 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0004 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0005 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0006 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0007 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3360 | 202 | 46 | 34 | 97 | 5 | 19 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0002 | 0/0 | 3360 | 51 | 21 | 9 | 15 | 3 | 3 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0003 | 0/0 | 3360 | 5 | 0 | 5 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0004 | 0/0 | 3372 | 3 | 0 | 0 | 3 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0005 | 0/0 | 3360 | 2 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0006 | 0/0 | 3360 | 2 | 2 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0007 | 0/1 | 3360 | 2 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0008 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0009 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0010 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0011 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0012 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0013 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0014 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0015 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0016 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0017 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| c0018 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9298 | 62 | 3 | 15 | 36 | 1 | 7 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0002 | 0/0 | 9298 | 40 | 15 | 7 | 15 | 1 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0003 | 0/0 | 9297 | 31 | 11 | 7 | 9 | 2 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0004 | 0/0 | 9301 | 12 | 1 | 2 | 6 | 0 | 3 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0005 | 0/0 | 9297 | 11 | 2 | 5 | 4 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0006 | 0/0 | 9290 | 6 | 0 | 1 | 5 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0007 | 0/0 | 9298 | 5 | 0 | 5 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0008 | 0/0 | 9298 | 5 | 0 | 0 | 1 | 2 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0009 | 0/0 | 9297 | 5 | 5 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0010 | 1/0 | 9298 | 4 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0011 | 0/0 | 9297 | 4 | 3 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0012 | 0/0 | 9298 | 4 | 0 | 0 | 4 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0013 | 0/0 | 9298 | 4 | 0 | 0 | 4 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0014 | 0/0 | 9304 | 3 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0015 | 0/0 | 9287 | 3 | 0 | 0 | 2 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0016 | 0/0 | 9297 | 3 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0017 | 0/1 | 9298 | 3 | 1 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0018 | 0/0 | 9300 | 3 | 0 | 0 | 3 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0019 | 0/0 | 9286 | 2 | 0 | 0 | 1 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0020 | 0/0 | 9287 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0021 | 0/0 | 9287 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0022 | 0/0 | 9287 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0023 | 0/0 | 9298 | 2 | 2 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0024 | 0/0 | 9301 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0025 | 0/0 | 9298 | 2 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0026 | 0/0 | 9297 | 2 | 0 | 1 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0027 | 0/0 | 9298 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0028 | 0/0 | 9301 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0029 | 0/0 | 9298 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0030 | 0/0 | 9305 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0031 | 0/0 | 9305 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0032 | 0/0 | 9290 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0033 | 0/0 | 9289 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0034 | 0/0 | 9289 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0035 | 0/0 | 9287 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0036 | 0/0 | 9287 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0037 | 0/0 | 9287 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0038 | 0/0 | 9286 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0039 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0040 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0041 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0042 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0043 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0044 | 0/0 | 9298 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0045 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0046 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0047 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0048 | 0/0 | 9297 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0049 | 0/0 | 9297 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0050 | 0/0 | 9297 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0051 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0052 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0053 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0054 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0055 | 0/0 | 9297 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0056 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0057 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0058 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0059 | 0/0 | 9298 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0060 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0061 | 0/0 | 9297 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0062 | 0/0 | 9297 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0063 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0064 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0065 | 0/0 | 9298 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0066 | 0/0 | 9301 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0067 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0068 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0069 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0070 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0071 | 0/0 | 9298 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0072 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0073 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0074 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0075 | 0/0 | 9297 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0076 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| t0077 | 0/0 | 9298 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3360 | 202 | 46 | 34 | 97 | 5 | 19 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002 | 0/0 | 3360 | 51 | 21 | 9 | 15 | 3 | 3 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0005 | 0/0 | 3360 | 2 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0006 | 0/0 | 3360 | 2 | 2 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0007 | 0/1 | 3360 | 2 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0008 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0009 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0012 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0013 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0014 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0016 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0018 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0002c0003 | 0/0 | 3360 | 5 | 0 | 5 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0003c0004 | 0/0 | 3372 | 3 | 0 | 0 | 3 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0004c0011 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0005c0010 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0006c0015 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0007c0017 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12657 | 55 | 3 | 14 | 32 | 1 | 5 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0002 | 0/0 | 12657 | 39 | 15 | 7 | 14 | 1 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0004 | 0/0 | 12660 | 10 | 1 | 2 | 5 | 0 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0005 | 0/0 | 12656 | 10 | 2 | 4 | 4 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0006 | 0/0 | 12649 | 5 | 0 | 0 | 5 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0008 | 0/0 | 12657 | 5 | 0 | 0 | 1 | 2 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0009 | 0/0 | 12656 | 5 | 5 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0010 | 1/0 | 12657 | 4 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0012 | 0/0 | 12657 | 4 | 0 | 0 | 4 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0013 | 0/0 | 12657 | 3 | 0 | 0 | 3 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0015 | 0/0 | 12646 | 3 | 0 | 0 | 2 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0016 | 0/0 | 12656 | 3 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0017 | 0/0 | 12657 | 2 | 1 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0018 | 0/0 | 12659 | 3 | 0 | 0 | 3 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0020 | 0/0 | 12646 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0021 | 0/0 | 12646 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0022 | 0/0 | 12646 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0024 | 0/0 | 12660 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0027 | 0/0 | 12657 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0028 | 0/0 | 12660 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0029 | 0/0 | 12657 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0030 | 0/0 | 12664 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0032 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0033 | 0/0 | 12648 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0034 | 0/0 | 12648 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0035 | 0/0 | 12646 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0036 | 0/0 | 12646 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0038 | 0/0 | 12645 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0039 | 0/0 | 12636 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0042 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0043 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0044 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0046 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0047 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0048 | 0/0 | 12656 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0051 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0052 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0053 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0054 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0055 | 0/0 | 12656 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0056 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0057 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0058 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0059 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0060 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0063 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0065 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0066 | 0/0 | 12660 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0067 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0068 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0069 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0070 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0071 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0072 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0073 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0074 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0076 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0001t0077 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0003 | 0/0 | 12656 | 31 | 11 | 7 | 9 | 2 | 2 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0011 | 0/0 | 12656 | 4 | 3 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0014 | 0/0 | 12663 | 3 | 3 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0019 | 0/0 | 12645 | 2 | 0 | 0 | 1 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0026 | 0/0 | 12656 | 2 | 0 | 1 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0031 | 0/0 | 12664 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0040 | 0/0 | 12636 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0041 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0049 | 0/0 | 12656 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0050 | 0/0 | 12656 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0061 | 0/0 | 12656 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0062 | 0/0 | 12656 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0064 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0002t0075 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0005t0025 | 0/0 | 12657 | 2 | 0 | 1 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0006t0023 | 0/0 | 12657 | 2 | 2 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0007t0005 | 0/0 | 12656 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0007t0017 | 0/1 | 12657 | 1 | 0 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0008t0001 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0009t0006 | 0/0 | 12649 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0012t0045 | 0/0 | 12656 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0013t0001 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0014t0004 | 0/0 | 12660 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0016t0001 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0001c0018t0004 | 0/0 | 12660 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0002c0003t0007 | 0/0 | 12657 | 5 | 0 | 5 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0003c0004t0001 | 0/0 | 12669 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0003c0004t0002 | 0/0 | 12669 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0003c0004t0037 | 0/0 | 12658 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0004c0011t0001 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0005c0010t0013 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0006c0015t0001 | 0/0 | 12657 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| a0007c0017t0001 | 0/0 | 12657 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | copy fasta | chr7 | 45569368 | 45728116 |
| 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 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0010g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0010g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0013g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0015g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0016g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0017g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0018g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0018g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0021g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0022g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0024g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0027g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0028g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0028g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0029g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0029g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0030g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0032g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0033g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0034g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0035g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0038g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0039g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0042g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0043g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0044g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0046g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0047g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0048g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0051g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0052g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0053g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0054g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0055g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0056g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0057g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0058g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0059g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0060g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0063g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0065g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0066g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0067g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0068g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0069g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0070g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0071g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0072g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0073g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0074g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0076g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0001t0077g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0011g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0019g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0019g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0026g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0026g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0031g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0040g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0041g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0049g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0050g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0061g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0062g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0064g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0002t0075g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0005t0025g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0005t0025g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0006t0023g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0006t0023g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0007t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0007t0017g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0009t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0012t0045g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0013t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0014t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0016t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0001c0018t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0002c0003t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0002c0003t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0002c0003t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0002c0003t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0002c0003t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0003c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0003c0004t0037g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0004c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0005c0010t0013g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0006c0015t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| a0007c0017t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0165 | EUR | GBR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0008 | EUR | GBR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0141 | EUR | FIN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00408 | hp1 | a0001 | c0001 | t0036 | g0046 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00408 | hp2 | a0001 | c0001 | t0074 | g0224 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00423 | hp1 | a0001 | c0008 | t0001 | g0244 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00423 | hp2 | a0001 | c0001 | t0033 | g0043 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00438 | hp2 | a0001 | c0013 | t0001 | g0223 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00642 | hp1 | a0002 | c0003 | t0007 | g0129 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00673 | hp1 | a0003 | c0004 | t0001 | g0225 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | CHS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG00738 | hp2 | a0001 | c0001 | t0044 | g0118 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0131 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0120 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01106 | hp1 | a0001 | c0002 | t0026 | g0005 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01106 | hp2 | a0001 | c0005 | t0025 | g0122 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01167 | hp1 | a0001 | c0016 | t0001 | g0138 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01175 | hp2 | a0002 | c0003 | t0007 | g0161 | AMR | PUR | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0183 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01256 | hp1 | a0001 | c0001 | t0027 | g0004 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01257 | hp1 | a0002 | c0003 | t0007 | g0032 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0115 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01258 | hp1 | a0002 | c0003 | t0007 | g0031 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01258 | hp2 | a0001 | c0001 | t0027 | g0004 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01261 | hp1 | a0001 | c0001 | t0065 | g0210 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0119 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01358 | hp1 | a0001 | c0007 | t0005 | g0233 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01433 | hp2 | a0001 | c0002 | t0011 | g0167 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01496 | hp1 | a0001 | c0001 | t0028 | g0133 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01515 | hp1 | a0001 | c0002 | t0064 | g0094 | EUR | IBS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0193 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01952 | hp1 | a0001 | c0001 | t0028 | g0211 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01978 | hp1 | a0001 | c0001 | t0059 | g0157 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01981 | hp1 | a0001 | c0009 | t0006 | g0061 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01981 | hp2 | a0002 | c0003 | t0007 | g0033 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02027 | hp1 | a0001 | c0001 | t0054 | g0074 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02027 | hp2 | a0001 | c0001 | t0076 | g0219 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02056 | hp1 | a0001 | c0001 | t0072 | g0123 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02071 | hp1 | a0001 | c0002 | t0026 | g0264 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02071 | hp2 | a0001 | c0001 | t0012 | g0201 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02074 | hp1 | a0001 | c0002 | t0049 | g0007 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02080 | hp2 | a0001 | c0001 | t0047 | g0245 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02083 | hp2 | a0001 | c0014 | t0004 | g0164 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02132 | hp2 | a0001 | c0001 | t0015 | g0056 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02155 | hp1 | a0001 | c0002 | t0062 | g0190 | EAS | CDX | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02155 | hp2 | a0003 | c0004 | t0002 | g0136 | EAS | CDX | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02258 | hp2 | a0001 | c0001 | t0068 | g0180 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02280 | hp1 | a0001 | c0002 | t0011 | g0142 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0195 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02451 | hp2 | a0001 | c0002 | t0011 | g0014 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02647 | hp2 | a0001 | c0001 | t0063 | g0026 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02683 | hp2 | a0001 | c0001 | t0052 | g0256 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02723 | hp1 | a0001 | c0001 | t0030 | g0100 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02723 | hp2 | a0001 | c0002 | t0075 | g0020 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0128 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02735 | hp2 | a0001 | c0001 | t0058 | g0071 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02809 | hp1 | a0001 | c0001 | t0066 | g0024 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02809 | hp2 | a0001 | c0001 | t0053 | g0236 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02818 | hp2 | a0001 | c0002 | t0014 | g0101 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0117 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02896 | hp1 | a0001 | c0002 | t0014 | g0099 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02922 | hp1 | a0001 | c0001 | t0071 | g0111 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02970 | hp2 | a0001 | c0001 | t0043 | g0146 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02976 | hp2 | a0001 | c0001 | t0039 | g0150 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03017 | hp1 | a0001 | c0001 | t0056 | g0241 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03041 | hp2 | a0001 | c0002 | t0040 | g0149 | AFR | GWD | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0098 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03139 | hp1 | a0001 | c0002 | t0011 | g0112 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03195 | hp2 | a0001 | c0002 | t0041 | g0082 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03209 | hp1 | a0001 | c0012 | t0045 | g0035 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0235 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03239 | hp1 | a0001 | c0001 | t0057 | g0010 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03239 | hp2 | a0001 | c0001 | t0051 | g0254 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03453 | hp2 | a0001 | c0001 | t0060 | g0019 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03492 | hp2 | a0004 | c0011 | t0001 | g0178 | SAS | PJL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03516 | hp1 | a0001 | c0001 | t0042 | g0029 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | ESN | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03579 | hp2 | a0001 | c0001 | t0070 | g0065 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0048 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03688 | hp2 | a0001 | c0001 | t0077 | g0012 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03942 | hp1 | a0001 | c0005 | t0025 | g0173 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0258 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0013 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04184 | hp1 | a0001 | c0002 | t0019 | g0038 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0110 | SAS | BEB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04228 | hp1 | a0007 | c0017 | t0001 | g0153 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG04228 | hp2 | a0001 | c0001 | t0048 | g0064 | SAS | STU | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | YRI | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | YRI | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | CHB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18939 | hp2 | a0001 | c0001 | t0020 | g0039 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18941 | hp2 | a0001 | c0001 | t0067 | g0002 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18944 | hp1 | a0001 | c0002 | t0061 | g0263 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18948 | hp2 | a0001 | c0001 | t0018 | g0134 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0259 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18954 | hp2 | a0001 | c0001 | t0029 | g0203 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18957 | hp1 | a0001 | c0001 | t0024 | g0222 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18957 | hp2 | a0001 | c0001 | t0022 | g0057 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18959 | hp1 | a0001 | c0001 | t0013 | g0255 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18959 | hp2 | a0001 | c0001 | t0034 | g0047 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18960 | hp2 | a0003 | c0004 | t0037 | g0055 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18962 | hp1 | a0001 | c0001 | t0055 | g0105 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18966 | hp2 | a0001 | c0002 | t0019 | g0052 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18968 | hp1 | a0001 | c0001 | t0018 | g0139 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18977 | hp2 | a0001 | c0001 | t0029 | g0204 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18978 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0214 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18984 | hp2 | a0001 | c0001 | t0013 | g0227 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18994 | hp2 | a0001 | c0001 | t0021 | g0045 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18998 | hp1 | a0001 | c0001 | t0021 | g0060 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19001 | hp1 | a0001 | c0001 | t0024 | g0206 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19001 | hp2 | a0005 | c0010 | t0013 | g0246 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19003 | hp1 | a0001 | c0001 | t0038 | g0054 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19007 | hp2 | a0001 | c0001 | t0012 | g0213 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19009 | hp1 | a0001 | c0001 | t0032 | g0040 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0248 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0270 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19030 | hp1 | a0001 | c0001 | t0046 | g0072 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19030 | hp2 | a0001 | c0006 | t0023 | g0079 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19043 | hp2 | a0001 | c0006 | t0023 | g0078 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19056 | hp1 | a0001 | c0001 | t0022 | g0050 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19058 | hp2 | a0006 | c0015 | t0001 | g0243 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19060 | hp2 | a0001 | c0001 | t0018 | g0113 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0268 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19065 | hp2 | a0001 | c0001 | t0035 | g0058 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19079 | hp2 | a0001 | c0001 | t0073 | g0207 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19080 | hp1 | a0001 | c0001 | t0013 | g0166 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19083 | hp2 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19086 | hp1 | a0001 | c0002 | t0050 | g0260 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20129 | hp1 | a0001 | c0001 | t0069 | g0239 | AFR | ASW | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0272 | AFR | ASW | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0009 | EUR | TSI | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0130 | EUR | TSI | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20905 | hp1 | a0001 | c0018 | t0004 | g0154 | SAS | GIH | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02559 | hp1 | a0001 | c0002 | t0031 | g0184 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | ACB | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | USA | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| HG06807 | hp2 | a0001 | c0002 | t0014 | g0102 | AFR | USA | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | USA | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | USA | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0017 | g0234 | REF | REF | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0095 | REF | REF | ADCY1_chr7_45569368_45728116 | ADCY1 | chr7 | 45569368 | 45728116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45574559
|
C | CGCGGCGG others(5): Show |
1 | a0003 | 3 | HG00673.hp1 HG02155.hp2 NA18960.hp2 |
disruptive_inframe_insertion | MODERATE | c.32_43dupGCGGAGGCGG others(2): Show |
p.Gly11_Gly14dup | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 220/12657 | 44/3360 | 15/1119 | INFO_REALIGN_3_PRIME | chr7 | 45574559 | |
| chr7:45574791
|
C | T | 1 | a0007 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.248C>T | p.Ala83Val | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 424/12657 | 248/3360 | 83/1119 | chr7 | 45574791 | ||
| chr7:45678052
|
C | T | 1 | a0006 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1789C>T | p.Arg597Trp | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 9/20 | 1965/12657 | 1789/3360 | 597/1119 | chr7 | 45678052 | ||
| chr7:45686199
|
G | A | 1 | a0005 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.2311G>A | p.Gly771Arg | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/20 | 2487/12657 | 2311/3360 | 771/1119 | chr7 | 45686199 | ||
| chr7:45708350
|
G | A | 1 | a0002 | 5 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.2818G>A | p.Ala940Thr | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/20 | 2994/12657 | 2818/3360 | 940/1119 | chr7 | 45708350 | ||
| chr7:45713819
|
G | A | 1 | a0004 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.3184G>A | p.Gly1062Ser | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3360/12657 | 3184/3360 | 1062/1119 | chr7 | 45713819 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45574585
|
C | G | 1 | a0001c0018 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.42C>G | p.Gly14Gly | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 218/12657 | 42/3360 | 14/1119 | chr7 | 45574585 | ||
| chr7:45574621
|
G | A | 1 | a0001c0008 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.78G>A | p.Gly26Gly | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 254/12657 | 78/3360 | 26/1119 | chr7 | 45574621 | ||
| chr7:45574762
|
C | A | 1 | a0001c0009 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.219C>A | p.Gly73Gly | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 395/12657 | 219/3360 | 73/1119 | chr7 | 45574762 | ||
| chr7:45574777
|
C | G | 1 | a0001c0007 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.234C>G | p.Ala78Ala | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 410/12657 | 234/3360 | 78/1119 | chr7 | 45574777 | ||
| chr7:45574801
|
C | G | 1 | a0001c0016 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.258C>G | p.Pro86Pro | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 434/12657 | 258/3360 | 86/1119 | chr7 | 45574801 | ||
| chr7:45610486
|
C | T | 1 | a0001c0006 | 2 | NA19030.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.897C>T | p.His299His | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/20 | 1073/12657 | 897/3360 | 299/1119 | chr7 | 45610486 | ||
| chr7:45662163
|
C | T | 1 | a0001c0005 | 2 | HG01106.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.1554C>T | p.Phe518Phe | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/20 | 1730/12657 | 1554/3360 | 518/1119 | chr7 | 45662163 | ||
| chr7:45686183
|
C | T | 1 | a0001c0014 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.2295C>T | p.Leu765Leu | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/20 | 2471/12657 | 2295/3360 | 765/1119 | chr7 | 45686183 | ||
| chr7:45703674
|
C | T | 1 | a0001c0013 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.2646C>T | p.Ile882Ile | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/20 | 2822/12657 | 2646/3360 | 882/1119 | chr7 | 45703674 | ||
| chr7:45708445
|
C | T | 1 | a0001c0012 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2913C>T | p.Asn971Asn | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/20 | 3089/12657 | 2913/3360 | 971/1119 | chr7 | 45708445 | ||
| chr7:45713725
|
G | A | 1 | a0001c0002 | 51 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(48): Show |
synonymous_variant | LOW | c.3090G>A | p.Arg1030Arg | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3266/12657 | 3090/3360 | 1030/1119 | chr7 | 45713725 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45574398
|
C | T | 1 | a0001c0001t0077 | 1 | HG03688.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | chr7 | 45574398 | ||||||
| chr7:45574415
|
C | CCGCCCCG | 3 | a0001c0001t0030a0001c0002t0014a0001c0002t0031 | 5 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-114_-108dupCGCCCC others(1): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 107 | INFO_REALIGN_3_PRIME | chr7 | 45574415 | ||||
| chr7:45574444
|
GCCGCCCG others(4): Show |
G | 14 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(11): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-80delGCCCGCCC others(3): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 80 | INFO_REALIGN_3_PRIME | chr7 | 45574444 | ||||
| chr7:45574460
|
CCGCCCCG others(13): Show |
C | 2 | a0001c0001t0039a0001c0002t0040 | 2 | HG02976.hp2 HG03041.hp2 |
5_prime_UTR_variant | MODIFIER | c.-71_-52delGCCGCCCG others(12): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/20 | 52 | INFO_REALIGN_3_PRIME | chr7 | 45574460 | ||||
| chr7:45714006
|
G | A | 1 | a0001c0002t0041 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 11 | chr7 | 45714006 | |||||
| chr7:45714008
|
G | A | 1 | a0001c0006t0023 | 2 | NA19030.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 13 | chr7 | 45714008 | |||||
| chr7:45714133
|
C | G | 1 | a0001c0001t0076 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 138 | chr7 | 45714133 | |||||
| chr7:45714320
|
C | T | 4 | a0001c0002t0014a0001c0002t0031a0001c0002t0040others(1): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*325C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 325 | chr7 | 45714320 | |||||
| chr7:45714555
|
C | T | 16 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(13): Show | 62 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*560C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 560 | chr7 | 45714555 | |||||
| chr7:45714595
|
C | G | 89 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(86): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*600C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 600 | chr7 | 45714595 | |||||
| chr7:45714612
|
G | A | 3 | a0001c0001t0043a0001c0001t0044a0001c0012t0045 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 617 | chr7 | 45714612 | |||||
| chr7:45714913
|
A | G | 1 | a0001c0001t0020 | 2 | NA18939.hp2 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*918A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 918 | chr7 | 45714913 | |||||
| chr7:45714961
|
C | G | 4 | a0001c0002t0014a0001c0002t0031a0001c0002t0040others(1): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*966C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 966 | chr7 | 45714961 | |||||
| chr7:45714983
|
G | A | 18 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(15): Show | 69 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*988G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 988 | chr7 | 45714983 | |||||
| chr7:45714999
|
C | T | 1 | a0001c0001t0035 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1004 | chr7 | 45714999 | |||||
| chr7:45715232
|
G | A | 4 | a0001c0001t0016a0001c0001t0043a0001c0001t0046others(1): Show | 7 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1237 | chr7 | 45715232 | |||||
| chr7:45715414
|
G | T | 3 | a0001c0001t0005a0001c0001t0009a0001c0007t0005 | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1419G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1419 | chr7 | 45715414 | |||||
| chr7:45715621
|
A | G | 4 | a0001c0001t0016a0001c0001t0043a0001c0001t0046others(1): Show | 7 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1626 | chr7 | 45715621 | |||||
| chr7:45715725
|
G | A | 1 | a0001c0001t0047 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1730 | chr7 | 45715725 | |||||
| chr7:45715764
|
C | T | 1 | a0001c0001t0043 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 1769 | chr7 | 45715764 | |||||
| chr7:45716081
|
C | G | 1 | a0001c0001t0071 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2086C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2086 | chr7 | 45716081 | |||||
| chr7:45716142
|
C | T | 1 | a0001c0001t0016 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2147C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2147 | chr7 | 45716142 | |||||
| chr7:45716224
|
A | C | 1 | a0001c0012t0045 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2229 | chr7 | 45716224 | |||||
| chr7:45716283
|
A | G | 1 | a0001c0001t0028 | 2 | HG01496.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2288A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2288 | chr7 | 45716283 | |||||
| chr7:45716304
|
C | T | 1 | a0001c0001t0070 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2309C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2309 | chr7 | 45716304 | |||||
| chr7:45716447
|
G | A | 1 | a0001c0001t0048 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2452G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2452 | chr7 | 45716447 | |||||
| chr7:45716526
|
C | T | 1 | a0001c0001t0069 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2531C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 2531 | chr7 | 45716526 | |||||
| chr7:45717062
|
G | A | 3 | a0001c0002t0019a0001c0002t0049a0001c0002t0050 | 4 | HG02074.hp1 HG04184.hp1 NA18966.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3067G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3067 | chr7 | 45717062 | |||||
| chr7:45717063
|
C | T | 1 | a0001c0001t0068 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3068C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3068 | chr7 | 45717063 | |||||
| chr7:45717219
|
A | C | 1 | a0001c0001t0027 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3224A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3224 | chr7 | 45717219 | |||||
| chr7:45717295
|
C | A | 2 | a0001c0001t0017a0001c0007t0017 | 3 | HG00280.hp1 HG01891.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3300C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3300 | chr7 | 45717295 | |||||
| chr7:45717315
|
A | G | 1 | a0001c0001t0067 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3320A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3320 | chr7 | 45717315 | |||||
| chr7:45717398
|
C | G | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0028others(7): Show | 24 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3403C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3403 | chr7 | 45717398 | |||||
| chr7:45717704
|
C | T | 1 | a0001c0001t0071 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3709C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3709 | chr7 | 45717704 | |||||
| chr7:45717744
|
G | A | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0028others(6): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3749G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3749 | chr7 | 45717744 | |||||
| chr7:45717760
|
C | T | 1 | a0001c0001t0065 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3765C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3765 | chr7 | 45717760 | |||||
| chr7:45717878
|
T | C | 1 | a0001c0001t0051 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3883T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 3883 | chr7 | 45717878 | |||||
| chr7:45718128
|
C | A | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG00423.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4133C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4133 | chr7 | 45718128 | |||||
| chr7:45718191
|
A | AAG | 1 | a0001c0001t0018 | 3 | NA18948.hp2 NA18968.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4196_*4197insAG | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4197 | chr7 | 45718191 | |||||
| chr7:45718192
|
C | A | 1 | a0001c0001t0018 | 3 | NA18948.hp2 NA18968.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4197C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4197 | chr7 | 45718192 | |||||
| chr7:45718207
|
G | A | 30 | a0001c0001t0001a0001c0001t0015a0001c0001t0017others(27): Show | 92 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*4212G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4212 | chr7 | 45718207 | |||||
| chr7:45718248
|
A | G | 3 | a0001c0001t0005a0001c0001t0009a0001c0007t0005 | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4253A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4253 | chr7 | 45718248 | |||||
| chr7:45718506
|
G | T | 7 | a0001c0001t0068a0001c0002t0011a0001c0002t0014others(4): Show | 13 | HG01106.hp1 HG01433.hp2 HG02071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4511G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4511 | chr7 | 45718506 | |||||
| chr7:45718595
|
A | G | 1 | a0001c0001t0059 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4600A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4600 | chr7 | 45718595 | |||||
| chr7:45718754
|
G | A | 1 | a0001c0001t0060 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4759G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4759 | chr7 | 45718754 | |||||
| chr7:45718888
|
C | T | 5 | a0001c0001t0008a0001c0001t0057a0001c0001t0058others(2): Show | 9 | HG00140.hp2 HG00673.hp2 HG02735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4893C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 4893 | chr7 | 45718888 | |||||
| chr7:45719050
|
G | A | 3 | a0001c0001t0005a0001c0001t0009a0001c0007t0005 | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5055G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5055 | chr7 | 45719050 | |||||
| chr7:45719051
|
A | G | 1 | a0001c0012t0045 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5056A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5056 | chr7 | 45719051 | |||||
| chr7:45719059
|
C | T | 1 | a0001c0001t0068 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5064C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5064 | chr7 | 45719059 | |||||
| chr7:45719077
|
C | T | 1 | a0001c0001t0070 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5082C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5082 | chr7 | 45719077 | |||||
| chr7:45719168
|
G | C | 1 | a0001c0002t0061 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5173G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5173 | chr7 | 45719168 | |||||
| chr7:45719205
|
A | G | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0021others(3): Show | 13 | HG02071.hp2 NA18957.hp2 NA18959.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5210A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5210 | chr7 | 45719205 | |||||
| chr7:45719309
|
C | T | 1 | a0001c0001t0048 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5314C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5314 | chr7 | 45719309 | |||||
| chr7:45719317
|
A | C | 1 | a0001c0001t0016 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5322A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5322 | chr7 | 45719317 | |||||
| chr7:45719414
|
G | A | 1 | a0001c0001t0052 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5419G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5419 | chr7 | 45719414 | |||||
| chr7:45719538
|
T | C | 1 | a0001c0001t0072 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5543T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5543 | chr7 | 45719538 | |||||
| chr7:45719663
|
C | T | 27 | a0001c0001t0001a0001c0001t0015a0001c0001t0017others(24): Show | 89 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*5668C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5668 | chr7 | 45719663 | |||||
| chr7:45719727
|
G | A | 1 | a0001c0001t0060 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5732G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5732 | chr7 | 45719727 | |||||
| chr7:45719834
|
C | A | 2 | a0001c0001t0012a0001c0001t0021 | 6 | HG02071.hp2 NA18978.hp2 NA18983.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5839C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 5839 | chr7 | 45719834 | |||||
| chr7:45720124
|
C | T | 1 | a0001c0005t0025 | 2 | HG01106.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6129C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6129 | chr7 | 45720124 | |||||
| chr7:45720275
|
C | T | 1 | a0001c0001t0056 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6280C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6280 | chr7 | 45720275 | |||||
| chr7:45720294
|
T | C | 12 | a0001c0001t0004a0001c0001t0006a0001c0001t0024others(9): Show | 27 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6299T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6299 | chr7 | 45720294 | |||||
| chr7:45720447
|
C | T | 1 | a0003c0004t0037 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6452C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6452 | chr7 | 45720447 | |||||
| chr7:45720513
|
CA | C | 27 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(24): Show | 79 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*6534delA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6534 | INFO_REALIGN_3_PRIME | chr7 | 45720513 | ||||
| chr7:45720664
|
C | T | 1 | a0001c0002t0050 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6669C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6669 | chr7 | 45720664 | |||||
| chr7:45720689
|
T | G | 1 | a0001c0002t0011 | 4 | HG01433.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6694T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6694 | chr7 | 45720689 | |||||
| chr7:45720762
|
T | A | 1 | a0001c0001t0063 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6767T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6767 | chr7 | 45720762 | |||||
| chr7:45720958
|
G | T | 1 | a0001c0001t0054 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6963G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 6963 | chr7 | 45720958 | |||||
| chr7:45721025
|
A | G | 1 | a0001c0012t0045 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7030A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7030 | chr7 | 45721025 | |||||
| chr7:45721164
|
T | C | 1 | a0001c0001t0073 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7169T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7169 | chr7 | 45721164 | |||||
| chr7:45721235
|
T | C | 2 | a0001c0001t0016a0001c0001t0046 | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7240T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7240 | chr7 | 45721235 | |||||
| chr7:45721253
|
A | G | 2 | a0001c0001t0016a0001c0001t0046 | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7258A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7258 | chr7 | 45721253 | |||||
| chr7:45721474
|
C | T | 1 | a0001c0001t0046 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7479C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7479 | chr7 | 45721474 | |||||
| chr7:45721595
|
T | G | 20 | a0001c0001t0016a0001c0001t0042a0001c0001t0046others(17): Show | 59 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*7600T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7600 | chr7 | 45721595 | |||||
| chr7:45721752
|
G | A | 3 | a0001c0001t0005a0001c0001t0009a0001c0007t0005 | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7757G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7757 | chr7 | 45721752 | |||||
| chr7:45721880
|
T | C | 1 | a0001c0001t0069 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7885T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7885 | chr7 | 45721880 | |||||
| chr7:45721965
|
G | A | 2 | a0001c0001t0016a0001c0001t0046 | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7970G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 7970 | chr7 | 45721965 | |||||
| chr7:45722175
|
C | T | 2 | a0001c0001t0029a0001c0001t0060 | 3 | HG03453.hp2 NA18954.hp2 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8180C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8180 | chr7 | 45722175 | |||||
| chr7:45722274
|
T | C | 1 | a0001c0001t0056 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8279T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8279 | chr7 | 45722274 | |||||
| chr7:45722353
|
A | C | 19 | a0001c0001t0016a0001c0001t0042a0001c0001t0046others(16): Show | 58 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*8358A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8358 | chr7 | 45722353 | |||||
| chr7:45722488
|
C | A | 1 | a0001c0001t0074 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8493C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8493 | chr7 | 45722488 | |||||
| chr7:45722553
|
C | T | 1 | a0001c0001t0009 | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8558C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8558 | chr7 | 45722553 | |||||
| chr7:45722603
|
T | C | 1 | a0001c0001t0057 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8608T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 8608 | chr7 | 45722603 | |||||
| chr7:45723088
|
A | AAAT | 11 | a0001c0001t0004a0001c0001t0006a0001c0001t0024others(8): Show | 26 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*9096_*9098dupTAA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 9099 | INFO_REALIGN_3_PRIME | chr7 | 45723088 | ||||
| chr7:45723097
|
G | A | 19 | a0001c0001t0016a0001c0001t0042a0001c0001t0046others(16): Show | 58 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*9102G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 20/20 | 9102 | chr7 | 45723097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45575276
|
G | A | 2 | a0001c0002t0003g0006a0001c0002t0026g0005 | 2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.639+94G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45575276 | ||||||
| chr7:45575584
|
G | A | 1 | a0001c0002t0049g0007 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.639+402G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45575584 | ||||||
| chr7:45575586
|
C | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(77): Show | 82 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.639+404C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45575586 | ||||||
| chr7:45575650
|
C | T | 1 | a0001c0002t0003g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.639+468C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45575650 | ||||||
| chr7:45576006
|
T | C | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.639+824T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576006 | ||||||
| chr7:45576028
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.639+846G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576028 | ||||||
| chr7:45576029
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.639+847C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576029 | ||||||
| chr7:45576047
|
GT | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(166): Show | 172 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.639+867delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45576047 | |||||
| chr7:45576134
|
A | C | 1 | a0001c0002t0003g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.639+952A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576134 | ||||||
| chr7:45576184
|
C | T | 139 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(136): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.639+1002C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576184 | ||||||
| chr7:45576281
|
G | A | 37 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.639+1099G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576281 | ||||||
| chr7:45576357
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(269): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.639+1175A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576357 | ||||||
| chr7:45576476
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0036others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.639+1294C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576476 | ||||||
| chr7:45576514
|
G | A | 36 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0208others(33): Show | 36 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.639+1332G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576514 | ||||||
| chr7:45576532
|
A | C | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639+1350A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576532 | ||||||
| chr7:45576614
|
G | T | 1 | a0001c0001t0002g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.639+1432G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576614 | ||||||
| chr7:45576783
|
C | T | 1 | a0001c0001t0005g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.639+1601C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576783 | ||||||
| chr7:45576905
|
G | C | 2 | a0001c0001t0002g0097a0001c0001t0016g0098 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.639+1723G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576905 | ||||||
| chr7:45576938
|
A | G | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+1756A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45576938 | ||||||
| chr7:45577095
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.639+1913A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577095 | ||||||
| chr7:45577173
|
A | G | 1 | a0001c0001t0017g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.639+1991A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577173 | ||||||
| chr7:45577367
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0054g0074 | 2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.639+2185C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577367 | ||||||
| chr7:45577400
|
A | G | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.639+2218A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577400 | ||||||
| chr7:45577532
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.639+2350C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577532 | ||||||
| chr7:45577749
|
C | T | 1 | a0001c0002t0062g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.639+2567C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577749 | ||||||
| chr7:45577784
|
T | G | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+2602T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577784 | ||||||
| chr7:45577806
|
C | T | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG02258.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.639+2624C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45577806 | ||||||
| chr7:45578029
|
G | A | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+2847G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578029 | ||||||
| chr7:45578099
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639+2917C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578099 | ||||||
| chr7:45578338
|
A | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639+3156A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578338 | ||||||
| chr7:45578382
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(124): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.639+3200A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578382 | ||||||
| chr7:45578406
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(158): Show | 164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.639+3224C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578406 | ||||||
| chr7:45578484
|
G | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(88): Show | 93 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.639+3302G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578484 | ||||||
| chr7:45578840
|
C | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0036others(17): Show | 20 | HG00140.hp2 HG00673.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.639+3658C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578840 | ||||||
| chr7:45578893
|
A | G | 3 | a0001c0001t0002g0232a0001c0001t0005g0230a0001c0001t0005g0231 | 3 | NA18964.hp2 NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.639+3711A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578893 | ||||||
| chr7:45578914
|
T | C | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+3732T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578914 | ||||||
| chr7:45578971
|
T | G | 1 | a0001c0002t0049g0007 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.639+3789T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45578971 | ||||||
| chr7:45579023
|
C | T | 9 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG02027.hp1 HG02040.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.639+3841C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579023 | ||||||
| chr7:45579032
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0004g0198a0001c0001t0004g0199 | 3 | NA18942.hp1 NA18975.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.639+3850G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579032 | ||||||
| chr7:45579133
|
C | T | 9 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG02027.hp1 HG02040.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.639+3951C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579133 | ||||||
| chr7:45579187
|
T | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639+4005T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579187 | ||||||
| chr7:45579189
|
G | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+4007G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579189 | ||||||
| chr7:45579269
|
C | G | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.639+4087C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579269 | ||||||
| chr7:45579432
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(123): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.639+4250T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579432 | ||||||
| chr7:45579520
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.639+4338T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579520 | ||||||
| chr7:45579647
|
G | A | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.639+4465G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579647 | ||||||
| chr7:45579841
|
G | A | 1 | a0001c0002t0019g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.639+4659G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579841 | ||||||
| chr7:45579921
|
T | A | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+4739T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579921 | ||||||
| chr7:45579944
|
G | C | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG02258.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.639+4762G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579944 | ||||||
| chr7:45579945
|
TC | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG02027.hp1 HG02040.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+4770delC | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45579945 | |||||
| chr7:45579950
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.639+4768C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579950 | ||||||
| chr7:45579952
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.639+4770C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579952 | ||||||
| chr7:45579955
|
C | T | 1 | a0001c0001t0008g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.639+4773C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579955 | ||||||
| chr7:45579970
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(122): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.639+4788G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45579970 | ||||||
| chr7:45580421
|
C | T | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.639+5239C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580421 | ||||||
| chr7:45580683
|
G | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+5501G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580683 | ||||||
| chr7:45580687
|
G | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+5505G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580687 | ||||||
| chr7:45580707
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.639+5525C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580707 | ||||||
| chr7:45580725
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639+5543G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580725 | ||||||
| chr7:45580749
|
C | G | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0002t0011g0014 | 3 | HG02451.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.639+5567C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580749 | ||||||
| chr7:45580953
|
G | C | 2 | a0001c0001t0010g0025a0001c0012t0045g0035 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.639+5771G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45580953 | ||||||
| chr7:45581017
|
C | G | 4 | a0001c0001t0001g0271a0001c0001t0004g0273a0001c0001t0066g0024others(1): Show | 4 | HG01099.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+5835C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581017 | ||||||
| chr7:45581050
|
G | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG01106.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+5868G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581050 | ||||||
| chr7:45581102
|
C | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(82): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.639+5920C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581102 | ||||||
| chr7:45581217
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.639+6035T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581217 | ||||||
| chr7:45581292
|
C | T | 2 | a0001c0001t0005g0185a0001c0002t0031g0184 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.639+6110C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581292 | ||||||
| chr7:45581337
|
A | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639+6155A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581337 | ||||||
| chr7:45581361
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(123): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.639+6179C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581361 | ||||||
| chr7:45581388
|
C | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+6206C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581388 | ||||||
| chr7:45581491
|
C | T | 1 | a0001c0001t0010g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639+6309C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581491 | ||||||
| chr7:45581518
|
G | A | 5 | a0001c0001t0030g0100a0001c0002t0014g0099a0001c0002t0014g0101others(2): Show | 5 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+6336G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581518 | ||||||
| chr7:45581679
|
C | T | 4 | a0001c0001t0027g0004a0002c0003t0007g0031a0002c0003t0007g0032others(1): Show | 5 | HG01256.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+6497C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581679 | ||||||
| chr7:45581749
|
A | G | 1 | a0001c0002t0003g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.639+6567A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581749 | ||||||
| chr7:45581772
|
A | G | 2 | a0001c0001t0005g0182a0001c0002t0003g0181 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.639+6590A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581772 | ||||||
| chr7:45581776
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(159): Show | 165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.639+6594T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581776 | ||||||
| chr7:45581833
|
A | T | 1 | a0001c0002t0019g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.639+6651A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581833 | ||||||
| chr7:45581868
|
C | G | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.639+6686C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581868 | ||||||
| chr7:45581880
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(159): Show | 165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.639+6698T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581880 | ||||||
| chr7:45581928
|
G | A | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+6746G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45581928 | ||||||
| chr7:45582024
|
TCA | T | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.639+6846_639+6847d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45582024 | |||||
| chr7:45582106
|
A | G | 1 | a0001c0002t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.639+6924A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582106 | ||||||
| chr7:45582221
|
C | T | 3 | a0001c0001t0002g0097a0001c0001t0016g0098a0001c0001t0068g0180 | 3 | HG02258.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.639+7039C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582221 | ||||||
| chr7:45582349
|
C | G | 5 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+7167C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582349 | ||||||
| chr7:45582473
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.639+7291C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582473 | ||||||
| chr7:45582592
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.639+7410A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582592 | ||||||
| chr7:45582658
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639+7476C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582658 | ||||||
| chr7:45582728
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.639+7546G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582728 | ||||||
| chr7:45582763
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.639+7581C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582763 | ||||||
| chr7:45582776
|
C | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0240others(32): Show | 37 | HG00423.hp1 HG00642.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.639+7594C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582776 | ||||||
| chr7:45582904
|
C | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0092others(102): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.639+7722C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582904 | ||||||
| chr7:45582991
|
C | T | 7 | a0001c0001t0002g0036a0001c0001t0010g0025a0001c0001t0010g0037others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+7809C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45582991 | ||||||
| chr7:45583053
|
A | G | 1 | a0001c0001t0058g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.639+7871A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583053 | ||||||
| chr7:45583072
|
G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.639+7890G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583072 | ||||||
| chr7:45583140
|
G | A | 1 | a0001c0002t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.639+7958G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583140 | ||||||
| chr7:45583150
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | NA18962.hp1 NA18964.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+7968G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583150 | ||||||
| chr7:45583257
|
G | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG01106.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+8075G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583257 | ||||||
| chr7:45583403
|
G | A | 20 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0036others(17): Show | 20 | HG00140.hp2 HG00673.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.639+8221G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583403 | ||||||
| chr7:45583433
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.639+8251A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583433 | ||||||
| chr7:45583553
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.639+8371T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583553 | ||||||
| chr7:45583670
|
C | T | 1 | a0004c0011t0001g0178 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.639+8488C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583670 | ||||||
| chr7:45583709
|
C | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267 | 3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.639+8527C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583709 | ||||||
| chr7:45583713
|
T | C | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.639+8531T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583713 | ||||||
| chr7:45583744
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(122): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.639+8562G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583744 | ||||||
| chr7:45583797
|
C | T | 1 | a0001c0002t0062g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.639+8615C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583797 | ||||||
| chr7:45583855
|
G | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.639+8673G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583855 | ||||||
| chr7:45583909
|
A | T | 1 | a0001c0002t0026g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.639+8727A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583909 | ||||||
| chr7:45583937
|
G | GT | 27 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0168others(24): Show | 27 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.639+8783dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTT | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0010g0025others(4): Show | 7 | HG00438.hp1 HG01891.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+8782_639+8783d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0033g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.639+8768_639+8783d others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(13): Show |
4 | a0001c0001t0006g0044a0001c0001t0021g0045a0001c0001t0034g0047others(1): Show | 4 | HG00408.hp1 NA18959.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+8764_639+8783d others(22): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(14): Show |
2 | a0001c0001t0006g0049a0001c0001t0015g0048 | 2 | HG03688.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.639+8763_639+8783d others(23): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(15): Show |
3 | a0001c0001t0006g0051a0001c0001t0022g0050a0001c0002t0019g0052 | 3 | NA18966.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.639+8762_639+8783d others(24): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(16): Show |
2 | a0001c0001t0006g0053a0001c0001t0038g0054 | 2 | NA19003.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.639+8761_639+8783d others(25): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(17): Show |
2 | a0001c0001t0015g0056a0003c0004t0037g0055 | 2 | HG02132.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.639+8760_639+8783d others(26): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0022g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.639+8759_639+8783d others(27): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(20): Show |
1 | a0001c0001t0035g0058 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.639+8757_639+8783d others(29): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(23): Show |
2 | a0001c0001t0006g0059a0001c0002t0019g0038 | 2 | HG04184.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.639+8783_639+8784i others(32): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(26): Show |
1 | a0001c0001t0021g0060 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.639+8783_639+8784i others(35): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
G | GTTTTTTT others(28): Show |
1 | a0001c0009t0006g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.639+8783_639+8784i others(37): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
GT | G | 13 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(10): Show | 13 | HG01255.hp2 HG01515.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.639+8783delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583937
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0002t0003g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.639+8772_639+8783d others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583937 | |||||
| chr7:45583942
|
T | TTTG | 13 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0090others(10): Show | 14 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.639+8762_639+8763i others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583942 | |||||
| chr7:45583943
|
T | TTG | 90 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(87): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.639+8762_639+8763i others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45583943 | |||||
| chr7:45583944
|
T | TG | 5 | a0001c0001t0002g0075a0001c0001t0012g0201a0001c0001t0012g0202others(2): Show | 5 | HG02071.hp2 HG06807.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+8762_639+8763i others(3): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583944 | ||||||
| chr7:45583947
|
T | G | 1 | a0001c0002t0061g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.639+8765T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583947 | ||||||
| chr7:45583948
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(81): Show | 86 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.639+8766T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583948 | ||||||
| chr7:45583949
|
T | G | 5 | a0001c0001t0002g0075a0001c0001t0012g0201a0001c0001t0012g0202others(2): Show | 5 | HG02071.hp2 HG06807.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+8767T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583949 | ||||||
| chr7:45583950
|
T | G | 7 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+8768T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583950 | ||||||
| chr7:45583953
|
T | G | 12 | a0001c0001t0001g0240a0001c0001t0002g0187a0001c0001t0002g0188others(9): Show | 12 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.639+8771T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45583953 | ||||||
| chr7:45584006
|
G | C | 1 | a0002c0003t0007g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.640-8753G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584006 | ||||||
| chr7:45584196
|
G | C | 1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.640-8563G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584196 | ||||||
| chr7:45584329
|
C | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.640-8430C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584329 | ||||||
| chr7:45584340
|
C | T | 1 | a0001c0002t0062g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.640-8419C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584340 | ||||||
| chr7:45584350
|
G | A | 33 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.640-8409G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584350 | ||||||
| chr7:45584499
|
C | T | 1 | a0001c0001t0077g0012 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.640-8260C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584499 | ||||||
| chr7:45584843
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.640-7916T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584843 | ||||||
| chr7:45584844
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.640-7915T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584844 | ||||||
| chr7:45584850
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.640-7909G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584850 | ||||||
| chr7:45584893
|
G | T | 1 | a0001c0001t0069g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.640-7866G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584893 | ||||||
| chr7:45584953
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.640-7806T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45584953 | ||||||
| chr7:45585192
|
T | A | 1 | a0001c0001t0004g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.640-7567T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585192 | ||||||
| chr7:45585425
|
T | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.640-7334T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585425 | ||||||
| chr7:45585439
|
CT | C | 28 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(25): Show | 29 | HG00280.hp2 HG01099.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.640-7299delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45585439 | |||||
| chr7:45585439
|
CTT | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(98): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.640-7300_640-7299d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45585439 | |||||
| chr7:45585439
|
CTTT | C | 10 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0187others(7): Show | 10 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-7301_640-7299d others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45585439 | |||||
| chr7:45585504
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640-7255C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585504 | ||||||
| chr7:45585528
|
C | T | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01884.hp2 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.640-7231C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585528 | ||||||
| chr7:45585648
|
A | G | 4 | a0001c0001t0002g0274a0001c0001t0005g0182a0001c0002t0003g0181others(1): Show | 4 | HG02135.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-7111A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585648 | ||||||
| chr7:45585649
|
T | C | 1 | a0001c0001t0033g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.640-7110T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585649 | ||||||
| chr7:45585714
|
C | T | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.640-7045C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585714 | ||||||
| chr7:45585722
|
A | G | 1 | a0001c0001t0002g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.640-7037A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45585722 | ||||||
| chr7:45586228
|
C | G | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640-6531C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586228 | ||||||
| chr7:45586294
|
G | A | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.640-6465G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586294 | ||||||
| chr7:45586381
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640-6378G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586381 | ||||||
| chr7:45586668
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0156a0001c0001t0001g0160others(5): Show | 8 | HG01928.hp1 HG01978.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.640-6091C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586668 | ||||||
| chr7:45586734
|
G | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(6): Show | 9 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.640-6025G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586734 | ||||||
| chr7:45586742
|
C | T | 1 | a0001c0002t0031g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.640-6017C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586742 | ||||||
| chr7:45586777
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.640-5982G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586777 | ||||||
| chr7:45586926
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.640-5833C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586926 | ||||||
| chr7:45586975
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640-5784A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45586975 | ||||||
| chr7:45587041
|
C | G | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640-5718C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45587041 | ||||||
| chr7:45587432
|
C | T | 4 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-5327C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45587432 | ||||||
| chr7:45587439
|
G | C | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.640-5320G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45587439 | ||||||
| chr7:45587918
|
T | C | 1 | a0001c0002t0003g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.640-4841T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45587918 | ||||||
| chr7:45588142
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.640-4617A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588142 | ||||||
| chr7:45588152
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640-4607G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588152 | ||||||
| chr7:45588243
|
G | C | 1 | a0001c0001t0004g0205 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.640-4516G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588243 | ||||||
| chr7:45588425
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.640-4334C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588425 | ||||||
| chr7:45588617
|
G | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-4142G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588617 | ||||||
| chr7:45588631
|
A | G | 1 | a0001c0018t0004g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.640-4128A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588631 | ||||||
| chr7:45588769
|
G | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-3990G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45588769 | ||||||
| chr7:45588869
|
A | ATG | 22 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(19): Show | 23 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.640-3866_640-3865d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45588869
|
A | ATGTG | 30 | a0001c0001t0002g0036a0001c0001t0006g0044a0001c0001t0006g0051others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.640-3868_640-3865d others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45588869
|
A | ATGTGTG | 9 | a0001c0001t0001g0027a0001c0001t0006g0049a0001c0001t0021g0060others(6): Show | 9 | HG00423.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.640-3870_640-3865d others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45588869
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0030a0001c0001t0010g0034a0001c0001t0016g0028 | 3 | HG01109.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.640-3872_640-3865d others(10): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45588869
|
ATG | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0106others(51): Show | 56 | HG00423.hp1 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.640-3866_640-3865d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45588869
|
ATGTGTGT others(1): Show |
A | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG02258.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.640-3872_640-3865d others(10): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45588869 | |||||
| chr7:45589164
|
C | T | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-3595C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589164 | ||||||
| chr7:45589203
|
C | T | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.640-3556C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589203 | ||||||
| chr7:45589204
|
G | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0036others(11): Show | 14 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.640-3555G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589204 | ||||||
| chr7:45589336
|
C | T | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.640-3423C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589336 | ||||||
| chr7:45589378
|
G | A | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.640-3381G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589378 | ||||||
| chr7:45589401
|
G | T | 1 | a0002c0003t0007g0033 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.640-3358G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589401 | ||||||
| chr7:45589473
|
C | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-3286C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589473 | ||||||
| chr7:45589488
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640-3271A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589488 | ||||||
| chr7:45589539
|
C | T | 2 | a0001c0001t0001g0186a0007c0017t0001g0153 | 2 | HG04228.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.640-3220C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589539 | ||||||
| chr7:45589615
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-3144C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589615 | ||||||
| chr7:45589643
|
T | G | 4 | a0001c0001t0006g0049a0001c0001t0021g0060a0001c0001t0034g0047others(1): Show | 4 | NA18959.hp2 NA18960.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-3116T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589643 | ||||||
| chr7:45589661
|
C | T | 2 | a0001c0001t0002g0174a0001c0001t0004g0273 | 2 | HG02080.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.640-3098C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589661 | ||||||
| chr7:45589719
|
T | A | 1 | a0001c0001t0022g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.640-3040T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589719 | ||||||
| chr7:45589791
|
G | GT | 18 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0228others(15): Show | 18 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.640-2958dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45589791 | |||||
| chr7:45589820
|
G | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.640-2939G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589820 | ||||||
| chr7:45589946
|
G | A | 2 | a0001c0001t0044g0118a0001c0002t0003g0115 | 2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.640-2813G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45589946 | ||||||
| chr7:45590041
|
G | T | 39 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(36): Show | 39 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.640-2718G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590041 | ||||||
| chr7:45590104
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.640-2655C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590104 | ||||||
| chr7:45590190
|
A | G | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-2569A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590190 | ||||||
| chr7:45590243
|
A | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-2516A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590243 | ||||||
| chr7:45590246
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(104): Show | 109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.640-2513C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590246 | ||||||
| chr7:45590357
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0010g0025a0001c0001t0010g0037others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-2402A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590357 | ||||||
| chr7:45590481
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.640-2278C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590481 | ||||||
| chr7:45590519
|
T | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(99): Show | 104 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.640-2240T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590519 | ||||||
| chr7:45590577
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-2182C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590577 | ||||||
| chr7:45590598
|
C | T | 15 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0228others(12): Show | 15 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.640-2161C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590598 | ||||||
| chr7:45590694
|
G | C | 1 | a0001c0002t0011g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.640-2065G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590694 | ||||||
| chr7:45590799
|
C | T | 3 | a0001c0001t0002g0097a0001c0001t0016g0098a0001c0001t0068g0180 | 3 | HG02258.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.640-1960C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590799 | ||||||
| chr7:45590896
|
G | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1863G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45590896 | ||||||
| chr7:45591022
|
G | A | 15 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0228others(12): Show | 15 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.640-1737G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591022 | ||||||
| chr7:45591085
|
T | C | 2 | a0001c0002t0003g0119a0001c0002t0003g0120 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.640-1674T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591085 | ||||||
| chr7:45591124
|
T | C | 1 | a0001c0001t0056g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.640-1635T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591124 | ||||||
| chr7:45591139
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.640-1620G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591139 | ||||||
| chr7:45591293
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640-1466C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591293 | ||||||
| chr7:45591303
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(167): Show | 173 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.640-1456C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591303 | ||||||
| chr7:45591477
|
A | G | 2 | a0001c0001t0039g0150a0001c0002t0040g0149 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.640-1282A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591477 | ||||||
| chr7:45591667
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0010g0025a0001c0001t0010g0037others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1092C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591667 | ||||||
| chr7:45591749
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0010g0025a0001c0001t0010g0037others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1010G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591749 | ||||||
| chr7:45591765
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.640-994G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591765 | ||||||
| chr7:45591828
|
C | T | 2 | a0001c0002t0014g0101a0001c0002t0014g0102 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.640-931C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591828 | ||||||
| chr7:45591849
|
T | A | 1 | a0001c0002t0003g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.640-910T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591849 | ||||||
| chr7:45591970
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-789C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591970 | ||||||
| chr7:45591986
|
C | T | 1 | a0001c0001t0039g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.640-773C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45591986 | ||||||
| chr7:45592040
|
G | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.640-719G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592040 | ||||||
| chr7:45592046
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.640-713G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592046 | ||||||
| chr7:45592053
|
G | GT | 29 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(26): Show | 30 | HG00280.hp2 HG00609.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.640-693dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 45592053 | |||||
| chr7:45592078
|
T | C | 5 | a0001c0001t0001g0228a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02258.hp1 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-681T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592078 | ||||||
| chr7:45592290
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.640-469G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592290 | ||||||
| chr7:45592310
|
C | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 9 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.640-449C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592310 | ||||||
| chr7:45592409
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.640-350C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592409 | ||||||
| chr7:45592460
|
A | G | 6 | a0001c0001t0001g0228a0001c0001t0002g0148a0001c0001t0002g0187others(3): Show | 6 | HG00609.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-299A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592460 | ||||||
| chr7:45592492
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(149): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.640-267G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592492 | ||||||
| chr7:45592512
|
C | A | 1 | a0001c0001t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.640-247C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592512 | ||||||
| chr7:45592579
|
G | A | 24 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.640-180G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592579 | ||||||
| chr7:45592656
|
C | T | 1 | a0001c0001t0008g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.640-103C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592656 | ||||||
| chr7:45592680
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.640-79A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592680 | ||||||
| chr7:45592693
|
G | A | 26 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0006g0044others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.640-66G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 1/19 | chr7 | 45592693 | ||||||
| chr7:45593023
|
T | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+115T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593023 | ||||||
| chr7:45593043
|
A | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789+135A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593043 | ||||||
| chr7:45593089
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.789+181A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593089 | ||||||
| chr7:45593145
|
C | G | 1 | a0001c0002t0014g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.789+237C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593145 | ||||||
| chr7:45593219
|
G | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+311G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593219 | ||||||
| chr7:45593300
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(6): Show | 9 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+392G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593300 | ||||||
| chr7:45593369
|
G | A | 1 | a0001c0002t0011g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.789+461G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593369 | ||||||
| chr7:45593410
|
G | A | 2 | a0001c0001t0039g0150a0001c0002t0040g0149 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.789+502G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593410 | ||||||
| chr7:45593424
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789+516C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593424 | ||||||
| chr7:45593546
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+638G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593546 | ||||||
| chr7:45593889
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.789+981C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593889 | ||||||
| chr7:45593993
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.789+1085A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45593993 | ||||||
| chr7:45594081
|
G | C | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.789+1173G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594081 | ||||||
| chr7:45594136
|
G | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+1228G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594136 | ||||||
| chr7:45594336
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.789+1428A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594336 | ||||||
| chr7:45594526
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.789+1618C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594526 | ||||||
| chr7:45594704
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+1796A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594704 | ||||||
| chr7:45594723
|
T | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789+1815T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45594723 | ||||||
| chr7:45595131
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+2223T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595131 | ||||||
| chr7:45595221
|
C | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(82): Show | 87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.789+2313C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595221 | ||||||
| chr7:45595238
|
C | T | 2 | a0001c0001t0006g0051a0001c0001t0038g0054 | 2 | NA19003.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.789+2330C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595238 | ||||||
| chr7:45595709
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.789+2801T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595709 | ||||||
| chr7:45595784
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+2876G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595784 | ||||||
| chr7:45595950
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+3042T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595950 | ||||||
| chr7:45595995
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.789+3087G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45595995 | ||||||
| chr7:45596134
|
T | C | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.789+3226T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596134 | ||||||
| chr7:45596202
|
C | T | 37 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0208others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.789+3294C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596202 | ||||||
| chr7:45596232
|
C | T | 9 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0008g0008others(6): Show | 9 | HG00140.hp2 HG00673.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+3324C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596232 | ||||||
| chr7:45596357
|
T | TGG | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+3454_789+3455d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | 45596357 | |||||
| chr7:45596373
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.789+3465G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596373 | ||||||
| chr7:45596402
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0092others(108): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.789+3494C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596402 | ||||||
| chr7:45596505
|
C | A | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.789+3597C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596505 | ||||||
| chr7:45596566
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.789+3658A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596566 | ||||||
| chr7:45596622
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.789+3714C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596622 | ||||||
| chr7:45596623
|
C | T | 1 | a0001c0001t0006g0059 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.789+3715C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596623 | ||||||
| chr7:45596705
|
C | T | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.789+3797C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596705 | ||||||
| chr7:45596933
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+4025G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596933 | ||||||
| chr7:45596936
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0017g0193a0001c0005t0025g0122 | 3 | HG00738.hp1 HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.789+4028G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45596936 | ||||||
| chr7:45597017
|
A | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.789+4109A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597017 | ||||||
| chr7:45597181
|
C | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+4273C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597181 | ||||||
| chr7:45597268
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+4360T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597268 | ||||||
| chr7:45597269
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.789+4361C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597269 | ||||||
| chr7:45597357
|
A | G | 1 | a0003c0004t0001g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.789+4449A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597357 | ||||||
| chr7:45597519
|
T | TA | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+4612dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | 45597519 | |||||
| chr7:45597775
|
C | T | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.789+4867C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597775 | ||||||
| chr7:45597814
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.789+4906A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45597814 | ||||||
| chr7:45598364
|
C | T | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.789+5456C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45598364 | ||||||
| chr7:45598498
|
A | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(30): Show | 34 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.789+5590A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45598498 | ||||||
| chr7:45598547
|
T | C | 1 | a0001c0002t0061g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.789+5639T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45598547 | ||||||
| chr7:45598641
|
C | T | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 22 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.789+5733C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45598641 | ||||||
| chr7:45599254
|
T | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+6346T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599254 | ||||||
| chr7:45599550
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+6642C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599550 | ||||||
| chr7:45599585
|
C | G | 80 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.789+6677C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599585 | ||||||
| chr7:45599632
|
G | GT | 67 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(64): Show | 68 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.789+6736dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | 45599632 | |||||
| chr7:45599677
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.789+6769A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599677 | ||||||
| chr7:45599715
|
C | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267 | 3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.789+6807C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599715 | ||||||
| chr7:45599767
|
C | T | 7 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+6859C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599767 | ||||||
| chr7:45599824
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+6916C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599824 | ||||||
| chr7:45599825
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+6917C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599825 | ||||||
| chr7:45599874
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(156): Show | 162 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.789+6966T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599874 | ||||||
| chr7:45599896
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.789+6988G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599896 | ||||||
| chr7:45599946
|
C | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(74): Show | 79 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.789+7038C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599946 | ||||||
| chr7:45599995
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.789+7087G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45599995 | ||||||
| chr7:45600015
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(157): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.789+7107T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600015 | ||||||
| chr7:45600079
|
G | T | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+7171G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600079 | ||||||
| chr7:45600144
|
C | G | 80 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.789+7236C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600144 | ||||||
| chr7:45600207
|
T | A | 2 | a0001c0002t0049g0007a0001c0014t0004g0164 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.789+7299T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600207 | ||||||
| chr7:45600483
|
G | A | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+7575G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600483 | ||||||
| chr7:45600680
|
C | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 10 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+7772C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600680 | ||||||
| chr7:45600683
|
A | G | 1 | a0001c0001t0057g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.789+7775A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600683 | ||||||
| chr7:45600710
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.789+7802C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600710 | ||||||
| chr7:45600779
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+7871G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600779 | ||||||
| chr7:45600806
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.789+7898C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45600806 | ||||||
| chr7:45601087
|
G | C | 1 | a0001c0001t0072g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.789+8179G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45601087 | ||||||
| chr7:45601169
|
A | G | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.789+8261A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45601169 | ||||||
| chr7:45601174
|
C | T | 1 | a0001c0001t0071g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.789+8266C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45601174 | ||||||
| chr7:45601569
|
T | C | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.789+8661T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45601569 | ||||||
| chr7:45601924
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-8455G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45601924 | ||||||
| chr7:45602384
|
G | A | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.790-7995G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602384 | ||||||
| chr7:45602447
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0002g0124 | 2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.790-7932G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602447 | ||||||
| chr7:45602613
|
A | G | 1 | a0001c0002t0040g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.790-7766A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602613 | ||||||
| chr7:45602644
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.790-7735G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602644 | ||||||
| chr7:45602668
|
C | T | 1 | a0001c0001t0004g0147 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.790-7711C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602668 | ||||||
| chr7:45602704
|
T | G | 1 | a0006c0015t0001g0243 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.790-7675T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602704 | ||||||
| chr7:45602735
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.790-7644A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45602735 | ||||||
| chr7:45603192
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.790-7187T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45603192 | ||||||
| chr7:45603208
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-7171C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45603208 | ||||||
| chr7:45603652
|
G | A | 11 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(8): Show | 11 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.790-6727G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45603652 | ||||||
| chr7:45603677
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0240others(29): Show | 34 | HG00423.hp1 HG00642.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.790-6702C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45603677 | ||||||
| chr7:45603929
|
A | G | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-6450A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45603929 | ||||||
| chr7:45604304
|
G | A | 7 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-6075G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45604304 | ||||||
| chr7:45604383
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.790-5996C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45604383 | ||||||
| chr7:45604820
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(146): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.790-5559T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45604820 | ||||||
| chr7:45605022
|
C | T | 2 | a0001c0013t0001g0223a0003c0004t0001g0225 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.790-5357C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605022 | ||||||
| chr7:45605029
|
A | G | 1 | a0001c0001t0024g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.790-5350A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605029 | ||||||
| chr7:45605116
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-5263A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605116 | ||||||
| chr7:45605227
|
TC | T | 3 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0077g0012 | 3 | HG00140.hp2 HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.790-5151delC | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605227 | ||||||
| chr7:45605254
|
A | G | 32 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(29): Show | 33 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.790-5125A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605254 | ||||||
| chr7:45605565
|
AT | A | 68 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.790-4803delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | 45605565 | |||||
| chr7:45605597
|
T | G | 1 | a0001c0008t0001g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.790-4782T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605597 | ||||||
| chr7:45605755
|
G | A | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-4624G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605755 | ||||||
| chr7:45605973
|
A | T | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 22 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-4406A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45605973 | ||||||
| chr7:45606016
|
T | C | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.790-4363T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606016 | ||||||
| chr7:45606049
|
C | T | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-4330C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606049 | ||||||
| chr7:45606161
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.790-4218C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606161 | ||||||
| chr7:45606261
|
G | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.790-4118G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606261 | ||||||
| chr7:45606305
|
C | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.790-4074C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606305 | ||||||
| chr7:45606505
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.790-3874T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606505 | ||||||
| chr7:45606729
|
T | A | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-3650T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606729 | ||||||
| chr7:45606786
|
A | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-3593A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606786 | ||||||
| chr7:45606886
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.790-3493C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45606886 | ||||||
| chr7:45607139
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(158): Show | 164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.790-3240A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607139 | ||||||
| chr7:45607189
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-3190C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607189 | ||||||
| chr7:45607234
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.790-3145C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607234 | ||||||
| chr7:45607253
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(253): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.790-3126A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607253 | ||||||
| chr7:45607270
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-3109G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607270 | ||||||
| chr7:45607357
|
A | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.790-3022A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607357 | ||||||
| chr7:45607692
|
A | T | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 22 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-2687A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45607692 | ||||||
| chr7:45608093
|
C | T | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-2286C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608093 | ||||||
| chr7:45608141
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-2238C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608141 | ||||||
| chr7:45608278
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-2101A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608278 | ||||||
| chr7:45608292
|
G | T | 3 | a0001c0001t0053g0236a0001c0001t0068g0180a0001c0001t0069g0239 | 3 | HG02258.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.790-2087G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608292 | ||||||
| chr7:45608551
|
C | T | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.790-1828C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608551 | ||||||
| chr7:45608785
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.790-1594G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608785 | ||||||
| chr7:45608985
|
T | C | 5 | a0001c0001t0030g0100a0001c0002t0014g0099a0001c0002t0014g0101others(2): Show | 5 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-1394T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45608985 | ||||||
| chr7:45609091
|
A | G | 1 | a0001c0001t0016g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.790-1288A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609091 | ||||||
| chr7:45609204
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(74): Show | 79 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.790-1175C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609204 | ||||||
| chr7:45609260
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-1119C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609260 | ||||||
| chr7:45609291
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.790-1088G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609291 | ||||||
| chr7:45609313
|
C | T | 1 | a0001c0002t0003g0131 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.790-1066C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609313 | ||||||
| chr7:45609314
|
G | A | 2 | a0001c0002t0003g0115a0001c0002t0011g0014 | 2 | HG01257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.790-1065G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609314 | ||||||
| chr7:45609324
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.790-1055C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609324 | ||||||
| chr7:45609383
|
T | C | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.790-996T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609383 | ||||||
| chr7:45609428
|
G | A | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.790-951G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609428 | ||||||
| chr7:45609564
|
T | C | 3 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267 | 3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.790-815T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609564 | ||||||
| chr7:45609669
|
G | A | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.790-710G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609669 | ||||||
| chr7:45609684
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.790-695C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609684 | ||||||
| chr7:45609714
|
C | T | 1 | a0001c0001t0052g0256 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.790-665C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609714 | ||||||
| chr7:45609720
|
A | G | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.790-659A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609720 | ||||||
| chr7:45609766
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.790-613A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609766 | ||||||
| chr7:45609976
|
G | A | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 22 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-403G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45609976 | ||||||
| chr7:45610177
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0156a0001c0001t0001g0160others(6): Show | 9 | HG01928.hp1 HG01978.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.790-202G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45610177 | ||||||
| chr7:45610289
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.790-90G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45610289 | ||||||
| chr7:45610294
|
G | A | 1 | a0001c0001t0016g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.790-85G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 2/19 | chr7 | 45610294 | ||||||
| chr7:45610651
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.908+154G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610651 | ||||||
| chr7:45610726
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.908+229G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610726 | ||||||
| chr7:45610729
|
A | G | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.908+232A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610729 | ||||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(725): Show |
1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.908+271_908+272ins others(732): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
1 | a0001c0001t0001g0003 | 2 | NA18954.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
7 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
2 | a0001c0001t0006g0049a0001c0001t0034g0047 | 2 | NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(727): Show |
3 | a0001c0001t0002g0132a0001c0002t0003g0018a0001c0002t0003g0151 | 3 | HG02965.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(734): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
249 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(246): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
2 | a0001c0001t0001g0108a0001c0001t0005g0220 | 2 | NA19081.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(723): Show |
1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.908+271_908+272ins others(730): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
2 | a0001c0001t0008g0258a0001c0001t0056g0241 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(726): Show |
1 | a0001c0001t0043g0146 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.908+271_908+272ins others(733): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610760
|
A | AGAGGTGA others(723): Show |
1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.908+271_908+272ins others(730): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610760 | |||||
| chr7:45610799
|
G | A | 1 | a0001c0001t0047g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.908+302G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610799 | ||||||
| chr7:45610818
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+321A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610818 | ||||||
| chr7:45610839
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+342T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610839 | ||||||
| chr7:45610845
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+348C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610845 | ||||||
| chr7:45610856
|
T | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+359T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610856 | ||||||
| chr7:45610858
|
G | A | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+361G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610858 | ||||||
| chr7:45610864
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+367A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610864 | ||||||
| chr7:45610950
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+453G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610950 | ||||||
| chr7:45610958
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+461G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610958 | ||||||
| chr7:45610960
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+463A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610960 | ||||||
| chr7:45610970
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+473G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610970 | ||||||
| chr7:45610983
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.908+486G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610983 | ||||||
| chr7:45610984
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.908+487T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610984 | ||||||
| chr7:45610996
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+499T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610996 | ||||||
| chr7:45610997
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+500G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45610997 | ||||||
| chr7:45610997
|
G | GTGGAGGT others(291): Show |
11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+508_908+509ins others(298): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45610997 | |||||
| chr7:45611006
|
G | A | 67 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.908+509G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611006 | ||||||
| chr7:45611009
|
G | A | 33 | a0001c0001t0001g0257a0001c0001t0006g0044a0001c0001t0006g0049others(30): Show | 33 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.908+512G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611009 | ||||||
| chr7:45611016
|
T | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(10): Show | 13 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.908+519T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611016 | ||||||
| chr7:45611016
|
T | TGTGGAGG others(290): Show |
1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.908+531_908+532ins others(297): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611016 | |||||
| chr7:45611031
|
A | AAAGTTGG others(291): Show |
10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+616_908+617ins others(298): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611031 | |||||
| chr7:45611031
|
A | AAAGTTGG others(291): Show |
245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(242): Show | 248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.908+616_908+617ins others(298): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611031 | |||||
| chr7:45611031
|
A | AAAGTTGG others(291): Show |
1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.908+616_908+617ins others(298): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611031 | |||||
| chr7:45611031
|
A | AAAGTTGG others(279): Show |
1 | a0001c0001t0002g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.908+616_908+617ins others(286): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611031 | |||||
| chr7:45611031
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0229 | 3 | NA18944.hp2 NA18955.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.908+534A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611031 | ||||||
| chr7:45611105
|
G | GATGGTGG others(291): Show |
3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+616_908+617ins others(298): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611105 | |||||
| chr7:45611162
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.908+665G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611162 | ||||||
| chr7:45611165
|
G | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.908+668G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611165 | ||||||
| chr7:45611272
|
T | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.908+775T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611272 | ||||||
| chr7:45611371
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.908+874C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611371 | ||||||
| chr7:45611444
|
C | T | 1 | a0001c0001t0016g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.908+947C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611444 | ||||||
| chr7:45611485
|
G | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.908+988G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611485 | ||||||
| chr7:45611499
|
T | C | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+1002T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611499 | ||||||
| chr7:45611637
|
G | GT | 49 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(46): Show | 50 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.908+1155dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611637 | |||||
| chr7:45611637
|
G | GTT | 24 | a0001c0001t0001g0092a0001c0001t0006g0044a0001c0001t0006g0049others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.908+1154_908+1155d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611637 | |||||
| chr7:45611637
|
GT | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0197others(85): Show | 90 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.908+1155delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45611637 | |||||
| chr7:45611779
|
A | G | 7 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.908+1282A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611779 | ||||||
| chr7:45611783
|
C | T | 44 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0257others(41): Show | 44 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.908+1286C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611783 | ||||||
| chr7:45611809
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.908+1312G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611809 | ||||||
| chr7:45611947
|
A | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+1450A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611947 | ||||||
| chr7:45611951
|
T | C | 1 | a0001c0001t0039g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.908+1454T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611951 | ||||||
| chr7:45611956
|
C | A | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.908+1459C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45611956 | ||||||
| chr7:45612028
|
G | A | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.908+1531G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612028 | ||||||
| chr7:45612169
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(270): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.908+1672A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612169 | ||||||
| chr7:45612185
|
CAAGTGGG others(16): Show |
C | 1 | a0001c0001t0001g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.908+1690_908+1712d others(25): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45612185 | |||||
| chr7:45612291
|
A | G | 1 | a0001c0002t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.908+1794A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612291 | ||||||
| chr7:45612744
|
G | A | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+2247G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612744 | ||||||
| chr7:45612753
|
A | G | 3 | a0002c0003t0007g0031a0002c0003t0007g0032a0002c0003t0007g0033 | 3 | HG01257.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.908+2256A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612753 | ||||||
| chr7:45612819
|
G | A | 1 | a0001c0001t0020g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.908+2322G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612819 | ||||||
| chr7:45612931
|
G | A | 1 | a0001c0001t0004g0147 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.908+2434G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45612931 | ||||||
| chr7:45613306
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+2809A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613306 | ||||||
| chr7:45613400
|
G | A | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+2903G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613400 | ||||||
| chr7:45613545
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.908+3048A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613545 | ||||||
| chr7:45613586
|
A | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+3089A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613586 | ||||||
| chr7:45613661
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.908+3164C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613661 | ||||||
| chr7:45613751
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.908+3254G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613751 | ||||||
| chr7:45613882
|
A | G | 44 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0257others(41): Show | 44 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.908+3385A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45613882 | ||||||
| chr7:45614018
|
T | A | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.908+3521T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614018 | ||||||
| chr7:45614207
|
GTA | G | 22 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.908+3712_908+3713d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45614207 | |||||
| chr7:45614226
|
A | G | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.908+3729A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614226 | ||||||
| chr7:45614242
|
A | G | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.908+3745A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614242 | ||||||
| chr7:45614398
|
A | T | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.908+3901A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614398 | ||||||
| chr7:45614534
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+4037C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614534 | ||||||
| chr7:45614628
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.908+4131G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614628 | ||||||
| chr7:45614703
|
A | G | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.908+4206A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614703 | ||||||
| chr7:45614711
|
C | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+4214C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614711 | ||||||
| chr7:45614716
|
T | C | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+4219T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614716 | ||||||
| chr7:45614934
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+4437G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45614934 | ||||||
| chr7:45615031
|
A | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | NA18962.hp1 NA18964.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+4534A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615031 | ||||||
| chr7:45615043
|
C | T | 1 | a0001c0001t0005g0220 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.908+4546C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615043 | ||||||
| chr7:45615140
|
C | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.908+4643C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615140 | ||||||
| chr7:45615208
|
G | T | 1 | a0001c0002t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.908+4711G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615208 | ||||||
| chr7:45615664
|
C | A | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+5167C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615664 | ||||||
| chr7:45615666
|
C | A | 19 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(16): Show | 20 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.908+5169C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45615666 | ||||||
| chr7:45615799
|
A | AAAG | 161 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(158): Show | 164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.908+5305_908+5307d others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr7 | 45615799 | |||||
| chr7:45616007
|
A | T | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.908+5510A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45616007 | ||||||
| chr7:45616503
|
T | C | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+6006T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45616503 | ||||||
| chr7:45616557
|
G | C | 1 | a0001c0002t0003g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.908+6060G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45616557 | ||||||
| chr7:45616570
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-6062G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45616570 | ||||||
| chr7:45617111
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-5521A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617111 | ||||||
| chr7:45617181
|
T | C | 80 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.909-5451T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617181 | ||||||
| chr7:45617182
|
G | T | 80 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.909-5450G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617182 | ||||||
| chr7:45617255
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.909-5377G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617255 | ||||||
| chr7:45617264
|
G | A | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-5368G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617264 | ||||||
| chr7:45617325
|
A | G | 68 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.909-5307A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617325 | ||||||
| chr7:45617345
|
T | A | 1 | a0001c0009t0006g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909-5287T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617345 | ||||||
| chr7:45617365
|
C | T | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.909-5267C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617365 | ||||||
| chr7:45617369
|
G | A | 6 | a0001c0002t0003g0015a0001c0002t0003g0017a0001c0002t0003g0018others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.909-5263G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617369 | ||||||
| chr7:45617992
|
A | G | 3 | a0001c0001t0039g0150a0001c0002t0003g0006a0001c0002t0040g0149 | 3 | HG02976.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-4640A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45617992 | ||||||
| chr7:45618270
|
T | C | 3 | a0002c0003t0007g0031a0002c0003t0007g0032a0002c0003t0007g0033 | 3 | HG01257.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.909-4362T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618270 | ||||||
| chr7:45618397
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(146): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.909-4235A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618397 | ||||||
| chr7:45618588
|
G | C | 66 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.909-4044G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618588 | ||||||
| chr7:45618761
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-3871G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618761 | ||||||
| chr7:45618897
|
A | C | 1 | a0001c0001t0069g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909-3735A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618897 | ||||||
| chr7:45618966
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.909-3666G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45618966 | ||||||
| chr7:45619348
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909-3284G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45619348 | ||||||
| chr7:45619464
|
T | A | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.909-3168T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45619464 | ||||||
| chr7:45619674
|
A | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.909-2958A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45619674 | ||||||
| chr7:45619710
|
G | T | 1 | a0001c0001t0002g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.909-2922G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45619710 | ||||||
| chr7:45619837
|
T | C | 1 | a0001c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.909-2795T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45619837 | ||||||
| chr7:45620194
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.909-2438C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620194 | ||||||
| chr7:45620195
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.909-2437G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620195 | ||||||
| chr7:45620206
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.909-2426A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620206 | ||||||
| chr7:45620239
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0135 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.909-2393G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620239 | ||||||
| chr7:45620327
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909-2305G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620327 | ||||||
| chr7:45620347
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.909-2285A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620347 | ||||||
| chr7:45620548
|
T | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0200others(78): Show | 83 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.909-2084T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620548 | ||||||
| chr7:45620748
|
G | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.909-1884G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620748 | ||||||
| chr7:45620819
|
C | T | 2 | a0001c0013t0001g0223a0003c0004t0001g0225 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.909-1813C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620819 | ||||||
| chr7:45620830
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.909-1802A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620830 | ||||||
| chr7:45620951
|
A | G | 1 | a0001c0001t0018g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.909-1681A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45620951 | ||||||
| chr7:45621090
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.909-1542G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621090 | ||||||
| chr7:45621135
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(158): Show | 164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.909-1497A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621135 | ||||||
| chr7:45621228
|
G | C | 1 | a0001c0014t0004g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.909-1404G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621228 | ||||||
| chr7:45621607
|
T | A | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 22 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.909-1025T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621607 | ||||||
| chr7:45621834
|
A | T | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.909-798A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621834 | ||||||
| chr7:45621875
|
A | G | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909-757A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621875 | ||||||
| chr7:45621920
|
G | A | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.909-712G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621920 | ||||||
| chr7:45621988
|
G | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 10 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.909-644G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45621988 | ||||||
| chr7:45622046
|
T | C | 1 | a0001c0002t0003g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.909-586T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45622046 | ||||||
| chr7:45622228
|
G | C | 2 | a0001c0001t0006g0051a0001c0001t0074g0224 | 2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.909-404G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45622228 | ||||||
| chr7:45622353
|
T | C | 1 | a0001c0002t0003g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.909-279T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45622353 | ||||||
| chr7:45622360
|
T | C | 23 | a0001c0001t0006g0044a0001c0001t0006g0049a0001c0001t0006g0051others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.909-272T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45622360 | ||||||
| chr7:45622435
|
G | A | 2 | a0001c0001t0005g0001a0001c0001t0005g0088 | 3 | HG01099.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.909-197G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 3/19 | chr7 | 45622435 | ||||||
| chr7:45622769
|
G | A | 1 | a0001c0001t0073g0207 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1020+26G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45622769 | ||||||
| chr7:45622837
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020+94T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45622837 | ||||||
| chr7:45623027
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1020+284C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623027 | ||||||
| chr7:45623028
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+285G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623028 | ||||||
| chr7:45623062
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1020+319G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623062 | ||||||
| chr7:45623170
|
C | T | 26 | a0001c0001t0001g0197a0001c0001t0001g0215a0001c0001t0002g0216others(23): Show | 26 | HG00438.hp2 HG00673.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1020+427C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623170 | ||||||
| chr7:45623175
|
G | T | 19 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(16): Show | 20 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1020+432G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623175 | ||||||
| chr7:45623244
|
C | T | 3 | a0001c0001t0053g0236a0001c0001t0068g0180a0001c0001t0069g0239 | 3 | HG02258.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1020+501C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623244 | ||||||
| chr7:45623374
|
G | T | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1020+631G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623374 | ||||||
| chr7:45623375
|
C | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1020+632C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623375 | ||||||
| chr7:45623728
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020+985C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623728 | ||||||
| chr7:45623845
|
G | A | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00609.hp2 HG02027.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1020+1102G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45623845 | ||||||
| chr7:45624032
|
A | G | 2 | a0001c0001t0070g0065a0001c0012t0045g0035 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1020+1289A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624032 | ||||||
| chr7:45624103
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1020+1360C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624103 | ||||||
| chr7:45624123
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1020+1380A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624123 | ||||||
| chr7:45624181
|
C | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0176a0001c0001t0001g0177others(67): Show | 72 | HG00423.hp1 HG00438.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1020+1438C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624181 | ||||||
| chr7:45624310
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1020+1567G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624310 | ||||||
| chr7:45624383
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG01261.hp1 HG01952.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+1640G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624383 | ||||||
| chr7:45624594
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+1851C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624594 | ||||||
| chr7:45624828
|
C | T | 2 | a0001c0001t0013g0227a0001c0001t0013g0255 | 2 | NA18959.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1020+2085C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624828 | ||||||
| chr7:45624829
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1020+2086T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624829 | ||||||
| chr7:45624842
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+2099T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624842 | ||||||
| chr7:45624993
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+2250T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45624993 | ||||||
| chr7:45625050
|
C | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+2307C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625050 | ||||||
| chr7:45625157
|
G | C | 1 | a0001c0001t0022g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1020+2414G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625157 | ||||||
| chr7:45625218
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1020+2475C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625218 | ||||||
| chr7:45625461
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1020+2718G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625461 | ||||||
| chr7:45625462
|
CACATATG others(25): Show |
C | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1020+2723_1020+275 others(36): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45625462 | |||||
| chr7:45625498
|
C | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0006t0023g0078others(1): Show | 4 | HG02970.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+2755C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625498 | ||||||
| chr7:45625505
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0215others(68): Show | 73 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1020+2762G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625505 | ||||||
| chr7:45625599
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1020+2856G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625599 | ||||||
| chr7:45625709
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+2966T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625709 | ||||||
| chr7:45625724
|
CT | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+2983delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45625724 | |||||
| chr7:45625879
|
G | A | 6 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0006g0044others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+3136G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625879 | ||||||
| chr7:45625969
|
A | G | 3 | a0001c0001t0006g0059a0001c0002t0019g0038a0001c0009t0006g0061 | 3 | HG01981.hp1 HG04184.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1020+3226A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625969 | ||||||
| chr7:45625996
|
G | T | 1 | a0001c0001t0017g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1020+3253G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45625996 | ||||||
| chr7:45626159
|
A | G | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+3416A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626159 | ||||||
| chr7:45626261
|
G | A | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1020+3518G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626261 | ||||||
| chr7:45626286
|
T | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+3543T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626286 | ||||||
| chr7:45626305
|
C | G | 10 | a0001c0001t0006g0049a0001c0001t0006g0051a0001c0001t0006g0053others(7): Show | 10 | HG01981.hp1 HG04184.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020+3562C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626305 | ||||||
| chr7:45626315
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+3572C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626315 | ||||||
| chr7:45626386
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+3643C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626386 | ||||||
| chr7:45626458
|
C | T | 26 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(23): Show | 26 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1020+3715C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626458 | ||||||
| chr7:45626565
|
C | A | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+3822C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626565 | ||||||
| chr7:45626654
|
T | C | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(14): Show | 18 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1020+3911T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626654 | ||||||
| chr7:45626677
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1020+3934A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626677 | ||||||
| chr7:45626739
|
A | G | 23 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1020+3996A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626739 | ||||||
| chr7:45626850
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1020+4107A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45626850 | ||||||
| chr7:45627102
|
G | A | 2 | a0001c0013t0001g0223a0003c0004t0001g0225 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1020+4359G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627102 | ||||||
| chr7:45627275
|
A | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(14): Show | 17 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1020+4532A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627275 | ||||||
| chr7:45627656
|
G | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1020+4913G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627656 | ||||||
| chr7:45627859
|
G | A | 1 | a0001c0001t0017g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1020+5116G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627859 | ||||||
| chr7:45627876
|
A | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(87): Show | 92 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1020+5133A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627876 | ||||||
| chr7:45627953
|
C | T | 1 | a0001c0001t0051g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1020+5210C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627953 | ||||||
| chr7:45627966
|
T | G | 1 | a0001c0001t0012g0214 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1020+5223T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45627966 | ||||||
| chr7:45628118
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1020+5375A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628118 | ||||||
| chr7:45628317
|
G | A | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1020+5574G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628317 | ||||||
| chr7:45628360
|
T | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(14): Show | 17 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1020+5617T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628360 | ||||||
| chr7:45628388
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1020+5645G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628388 | ||||||
| chr7:45628422
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1020+5679A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628422 | ||||||
| chr7:45628681
|
A | G | 24 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(21): Show | 25 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1020+5938A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628681 | ||||||
| chr7:45628759
|
G | A | 3 | a0001c0001t0002g0089a0001c0001t0005g0001a0001c0001t0005g0088 | 4 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+6016G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628759 | ||||||
| chr7:45628796
|
G | A | 1 | a0001c0005t0025g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1020+6053G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628796 | ||||||
| chr7:45628883
|
T | A | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1020+6140T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628883 | ||||||
| chr7:45628991
|
G | A | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+6248G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45628991 | ||||||
| chr7:45629152
|
A | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1020+6409A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629152 | ||||||
| chr7:45629169
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1020+6426G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629169 | ||||||
| chr7:45629431
|
C | T | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+6688C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629431 | ||||||
| chr7:45629490
|
A | G | 1 | a0001c0001t0028g0211 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1020+6747A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629490 | ||||||
| chr7:45629494
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+6751C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629494 | ||||||
| chr7:45629509
|
C | CT | 37 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1020+6786dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45629509 | |||||
| chr7:45629509
|
CT | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0092others(91): Show | 97 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1020+6786delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45629509 | |||||
| chr7:45629515
|
T | G | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1020+6772T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629515 | ||||||
| chr7:45629550
|
C | T | 5 | a0001c0001t0018g0113a0001c0001t0018g0134a0001c0001t0018g0139others(2): Show | 5 | NA18939.hp2 NA18948.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020+6807C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629550 | ||||||
| chr7:45629551
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+6808G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629551 | ||||||
| chr7:45629559
|
C | T | 1 | a0001c0002t0026g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1020+6816C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629559 | ||||||
| chr7:45629604
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1020+6861C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629604 | ||||||
| chr7:45629667
|
C | T | 68 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0091others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1020+6924C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629667 | ||||||
| chr7:45629675
|
C | T | 2 | a0001c0001t0002g0221a0001c0001t0073g0207 | 2 | NA19010.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1020+6932C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629675 | ||||||
| chr7:45629679
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+6936C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629679 | ||||||
| chr7:45629680
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1020+6937G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629680 | ||||||
| chr7:45629681
|
G | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(23): Show | 26 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1020+6938G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629681 | ||||||
| chr7:45629704
|
A | G | 7 | a0001c0001t0002g0036a0001c0001t0002g0076a0001c0001t0002g0077others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020+6961A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629704 | ||||||
| chr7:45629763
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+7020C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629763 | ||||||
| chr7:45629798
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0238others(34): Show | 39 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1020+7055C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629798 | ||||||
| chr7:45629809
|
G | A | 3 | a0001c0001t0006g0049a0001c0001t0006g0051a0001c0001t0034g0047 | 3 | NA18959.hp2 NA19056.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1020+7066G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629809 | ||||||
| chr7:45629814
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1020+7071C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629814 | ||||||
| chr7:45629819
|
G | A | 4 | a0001c0001t0002g0075a0001c0001t0002g0265a0001c0001t0002g0266others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+7076G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629819 | ||||||
| chr7:45629913
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+7170G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629913 | ||||||
| chr7:45629966
|
A | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+7223A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45629966 | ||||||
| chr7:45630091
|
C | G | 23 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.1020+7348C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630091 | ||||||
| chr7:45630137
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1020+7394G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630137 | ||||||
| chr7:45630215
|
G | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1020+7472G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630215 | ||||||
| chr7:45630225
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1020+7482T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630225 | ||||||
| chr7:45630379
|
G | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(265): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1020+7636G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630379 | ||||||
| chr7:45630488
|
C | T | 3 | a0001c0001t0001g0003a0001c0002t0050g0260a0006c0015t0001g0243 | 4 | NA18954.hp1 NA18998.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+7745C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630488 | ||||||
| chr7:45630604
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(250): Show | 256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1020+7861T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630604 | ||||||
| chr7:45630656
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+7913C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630656 | ||||||
| chr7:45630671
|
C | T | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1020+7928C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630671 | ||||||
| chr7:45630683
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1020+7940A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630683 | ||||||
| chr7:45630721
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1020+7978A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630721 | ||||||
| chr7:45630747
|
T | C | 2 | a0001c0001t0024g0222a0005c0010t0013g0246 | 2 | NA18957.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1020+8004T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45630747 | ||||||
| chr7:45631002
|
T | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+8259T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631002 | ||||||
| chr7:45631157
|
T | C | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+8414T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631157 | ||||||
| chr7:45631316
|
G | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(23): Show | 26 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1020+8573G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631316 | ||||||
| chr7:45631326
|
G | A | 1 | a0001c0002t0019g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1020+8583G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631326 | ||||||
| chr7:45631336
|
T | C | 1 | a0001c0001t0008g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1020+8593T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631336 | ||||||
| chr7:45631395
|
C | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+8652C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631395 | ||||||
| chr7:45631682
|
A | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+8939A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631682 | ||||||
| chr7:45631790
|
A | G | 25 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1020+9047A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45631790 | ||||||
| chr7:45632009
|
C | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+9266C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632009 | ||||||
| chr7:45632087
|
A | C | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1020+9344A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632087 | ||||||
| chr7:45632229
|
T | C | 1 | a0001c0002t0003g0247 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1020+9486T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632229 | ||||||
| chr7:45632417
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1020+9674A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632417 | ||||||
| chr7:45632516
|
AAAAATTC others(27): Show |
A | 34 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(31): Show | 34 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1020+9774_1020+980 others(38): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632516 | ||||||
| chr7:45632738
|
AT | A | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+10007delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45632738 | |||||
| chr7:45632773
|
T | C | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1020+10030T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632773 | ||||||
| chr7:45632868
|
G | T | 1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1020+10125G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45632868 | ||||||
| chr7:45633150
|
T | G | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0006t0023g0078others(1): Show | 4 | HG02970.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+10407T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633150 | ||||||
| chr7:45633170
|
G | A | 8 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(5): Show | 8 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+10427G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633170 | ||||||
| chr7:45633224
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+10481G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633224 | ||||||
| chr7:45633359
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1020+10616C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633359 | ||||||
| chr7:45633531
|
C | T | 1 | a0001c0001t0069g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1020+10788C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633531 | ||||||
| chr7:45633599
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+10856C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633599 | ||||||
| chr7:45633679
|
G | A | 1 | a0003c0004t0037g0055 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1020+10936G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633679 | ||||||
| chr7:45633717
|
G | A | 7 | a0001c0001t0001g0200a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01261.hp1 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020+10974G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633717 | ||||||
| chr7:45633750
|
C | G | 1 | a0001c0005t0025g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1020+11007C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633750 | ||||||
| chr7:45633757
|
G | A | 2 | a0001c0001t0016g0098a0001c0001t0071g0111 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1020+11014G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633757 | ||||||
| chr7:45633800
|
C | CA | 11 | a0001c0001t0001g0156a0001c0001t0001g0176a0001c0001t0008g0008others(8): Show | 11 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+11077dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45633800 | |||||
| chr7:45633800
|
CA | C | 47 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(44): Show | 48 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1020+11077delA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45633800 | |||||
| chr7:45633801
|
A | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+11058A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45633801 | ||||||
| chr7:45634293
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1020+11550G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634293 | ||||||
| chr7:45634425
|
GT | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(117): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1020+11698delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45634425 | |||||
| chr7:45634449
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0215others(69): Show | 74 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1020+11706A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634449 | ||||||
| chr7:45634456
|
T | C | 4 | a0001c0001t0006g0049a0001c0001t0006g0051a0001c0001t0034g0047others(1): Show | 4 | HG00408.hp2 NA18959.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+11713T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634456 | ||||||
| chr7:45634525
|
T | C | 1 | a0001c0001t0017g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1020+11782T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634525 | ||||||
| chr7:45634546
|
A | C | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+11803A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634546 | ||||||
| chr7:45634612
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1020+11869C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634612 | ||||||
| chr7:45634696
|
C | T | 1 | a0001c0002t0062g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1020+11953C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634696 | ||||||
| chr7:45634732
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1020+11989G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634732 | ||||||
| chr7:45634743
|
C | A | 1 | a0001c0001t0004g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1020+12000C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634743 | ||||||
| chr7:45634891
|
A | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0215others(69): Show | 74 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1020+12148A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45634891 | ||||||
| chr7:45635138
|
G | GT | 120 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0070others(117): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1020+12407dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635138 | |||||
| chr7:45635138
|
G | GTT | 21 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0187others(18): Show | 21 | HG00140.hp2 HG00673.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1020+12406_1020+12 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635138 | |||||
| chr7:45635143
|
T | C | 1 | a0001c0002t0003g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1020+12400T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635143 | ||||||
| chr7:45635160
|
A | G | 1 | a0003c0004t0001g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1020+12417A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635160 | ||||||
| chr7:45635247
|
T | C | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+12504T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635247 | ||||||
| chr7:45635268
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1020+12525C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635268 | ||||||
| chr7:45635297
|
A | G | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+12554A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635297 | ||||||
| chr7:45635479
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+12736C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635479 | ||||||
| chr7:45635503
|
G | A | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+12760G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635503 | ||||||
| chr7:45635601
|
G | GT | 45 | a0001c0001t0001g0027a0001c0001t0001g0093a0001c0001t0001g0103others(42): Show | 46 | HG00280.hp2 HG00438.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1020+12886dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
G | GTT | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0125others(7): Show | 10 | HG01358.hp2 HG01981.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+12885_1020+12 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
G | GTTT | 10 | a0001c0001t0001g0070a0001c0001t0002g0073a0001c0001t0002g0076others(7): Show | 10 | HG01167.hp1 HG01884.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+12884_1020+12 others(9): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
G | GTTTTTTT others(3): Show |
1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1020+12877_1020+12 others(16): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
G | T | 1 | a0001c0001t0027g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1020+12858G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635601 | ||||||
| chr7:45635601
|
GT | G | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0237others(14): Show | 17 | HG01257.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1020+12886delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
GTTTTTT | G | 21 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.1020+12881_1020+12 others(12): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1020+12876_1020+12 others(17): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+12875_1020+12 others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635601
|
GTTTTTTT others(9): Show |
G | 1 | a0004c0011t0001g0178 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1020+12871_1020+12 others(22): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45635601 | |||||
| chr7:45635613
|
T | G | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1020+12870T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635613 | ||||||
| chr7:45635614
|
T | G | 1 | a0001c0001t0056g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1020+12871T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635614 | ||||||
| chr7:45635629
|
T | C | 1 | a0001c0002t0003g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1020+12886T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635629 | ||||||
| chr7:45635661
|
C | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+12918C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635661 | ||||||
| chr7:45635787
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1021-12883G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635787 | ||||||
| chr7:45635810
|
G | C | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1021-12860G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635810 | ||||||
| chr7:45635832
|
A | G | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG02258.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1021-12838A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45635832 | ||||||
| chr7:45636180
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1021-12490A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636180 | ||||||
| chr7:45636405
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1021-12265A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636405 | ||||||
| chr7:45636601
|
C | T | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-12069C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636601 | ||||||
| chr7:45636625
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1021-12045C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636625 | ||||||
| chr7:45636633
|
C | T | 1 | a0007c0017t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1021-12037C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636633 | ||||||
| chr7:45636743
|
A | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(154): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1021-11927A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636743 | ||||||
| chr7:45636783
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1021-11887C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636783 | ||||||
| chr7:45636909
|
C | T | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-11761C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636909 | ||||||
| chr7:45636984
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1021-11686G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45636984 | ||||||
| chr7:45637532
|
G | A | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-11138G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637532 | ||||||
| chr7:45637537
|
C | A | 3 | a0001c0001t0001g0003a0001c0002t0050g0260a0006c0015t0001g0243 | 4 | NA18954.hp1 NA18998.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-11133C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637537 | ||||||
| chr7:45637586
|
G | A | 51 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1021-11084G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637586 | ||||||
| chr7:45637590
|
T | G | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1021-11080T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637590 | ||||||
| chr7:45637597
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1021-11073T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637597 | ||||||
| chr7:45637639
|
C | T | 1 | a0001c0001t0058g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1021-11031C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637639 | ||||||
| chr7:45637669
|
G | A | 1 | a0001c0002t0003g0268 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1021-11001G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637669 | ||||||
| chr7:45637765
|
A | G | 1 | a0001c0001t0017g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1021-10905A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637765 | ||||||
| chr7:45637814
|
G | T | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-10856G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637814 | ||||||
| chr7:45637877
|
G | T | 1 | a0001c0001t0002g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1021-10793G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45637877 | ||||||
| chr7:45638155
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1021-10515G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638155 | ||||||
| chr7:45638204
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0016g0235a0001c0012t0045g0035 | 3 | HG03209.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-10466G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638204 | ||||||
| chr7:45638432
|
G | C | 1 | a0001c0001t0076g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1021-10238G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638432 | ||||||
| chr7:45638481
|
CT | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(143): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1021-10172delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45638481 | |||||
| chr7:45638481
|
CTT | C | 7 | a0001c0001t0022g0057a0001c0001t0042g0029a0001c0001t0053g0236others(4): Show | 7 | HG01106.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021-10173_1021-10 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45638481 | |||||
| chr7:45638598
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0169 | 3 | NA18952.hp1 NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1021-10072A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638598 | ||||||
| chr7:45638664
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1021-10006G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638664 | ||||||
| chr7:45638683
|
A | G | 1 | a0001c0001t0006g0051 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1021-9987A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638683 | ||||||
| chr7:45638709
|
T | G | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 17 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1021-9961T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45638709 | ||||||
| chr7:45639046
|
A | G | 9 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG01071.hp1 HG01167.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1021-9624A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639046 | ||||||
| chr7:45639147
|
A | G | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0006t0023g0078others(1): Show | 4 | HG02970.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-9523A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639147 | ||||||
| chr7:45639165
|
A | C | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1021-9505A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639165 | ||||||
| chr7:45639422
|
A | G | 35 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(32): Show | 35 | HG00140.hp2 HG00673.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1021-9248A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639422 | ||||||
| chr7:45639448
|
A | C | 2 | a0001c0001t0002g0063a0001c0012t0045g0035 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1021-9222A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639448 | ||||||
| chr7:45639563
|
C | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0215others(68): Show | 73 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1021-9107C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639563 | ||||||
| chr7:45639710
|
C | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-8960C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639710 | ||||||
| chr7:45639749
|
C | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-8921C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639749 | ||||||
| chr7:45639765
|
A | G | 8 | a0001c0001t0006g0044a0001c0001t0021g0045a0001c0001t0022g0050others(5): Show | 8 | HG00408.hp1 HG00423.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-8905A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45639765 | ||||||
| chr7:45640043
|
A | G | 1 | a0001c0001t0004g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1021-8627A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45640043 | ||||||
| chr7:45640659
|
G | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0215others(68): Show | 73 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1021-8011G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45640659 | ||||||
| chr7:45641230
|
C | T | 4 | a0001c0002t0003g0247a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | NA18948.hp1 NA19004.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-7440C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641230 | ||||||
| chr7:45641256
|
C | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0006t0023g0078others(1): Show | 4 | HG02970.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-7414C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641256 | ||||||
| chr7:45641418
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1021-7252A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641418 | ||||||
| chr7:45641612
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(155): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1021-7058C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641612 | ||||||
| chr7:45641737
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(155): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1021-6933C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641737 | ||||||
| chr7:45641783
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(270): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1021-6887A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641783 | ||||||
| chr7:45641794
|
C | T | 3 | a0001c0001t0004g0066a0001c0001t0004g0127a0001c0001t0005g0194 | 3 | HG01109.hp2 HG01255.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1021-6876C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641794 | ||||||
| chr7:45641902
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1021-6768C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641902 | ||||||
| chr7:45641903
|
G | A | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-6767G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641903 | ||||||
| chr7:45641932
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0237a0001c0001t0002g0016a0001c0001t0028g0133others(1): Show | 4 | HG01496.hp1 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-6733_1021-672 others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(4): Show |
109 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0104others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1021-6734_1021-672 others(15): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0103a0001c0001t0002g0148a0001c0001t0046g0072others(1): Show | 4 | HG00609.hp1 HG02056.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-6735_1021-672 others(16): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0015g0056 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1021-6736_1021-672 others(17): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0027a0001c0001t0063g0026 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(20): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0008g0011 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(21): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0002g0218a0001c0001t0053g0236a0001c0001t0068g0180others(1): Show | 4 | HG02258.hp2 HG02809.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(22): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(12): Show |
19 | a0001c0001t0001g0197a0001c0001t0002g0062a0001c0001t0002g0137others(16): Show | 19 | HG02071.hp2 HG02080.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(23): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(13): Show |
11 | a0001c0001t0001g0215a0001c0001t0001g0253a0001c0001t0002g0232others(8): Show | 11 | HG00438.hp2 HG00673.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(24): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0002g0267a0001c0001t0005g0230a0001c0006t0023g0078others(1): Show | 4 | HG01167.hp2 NA19001.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(25): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(15): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0238a0001c0001t0001g0261others(17): Show | 22 | HG00609.hp2 HG00642.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(26): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(16): Show |
15 | a0001c0001t0001g0228a0001c0001t0001g0242a0001c0001t0001g0249others(12): Show | 15 | HG01358.hp1 HG01433.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(27): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(17): Show |
24 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(28): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(18): Show |
6 | a0001c0001t0001g0240a0001c0001t0002g0274a0001c0001t0006g0053others(3): Show | 6 | HG01346.hp1 HG02135.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(29): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(19): Show |
4 | a0001c0001t0002g0036a0001c0002t0003g0272a0001c0002t0019g0038others(1): Show | 4 | HG01167.hp1 HG03471.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(30): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0021g0045a0001c0001t0070g0065 | 2 | HG03579.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(31): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0057g0010a0001c0001t0076g0219 | 2 | HG02027.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(32): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0002g0189a0002c0003t0007g0032 | 2 | HG01257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(33): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(23): Show |
5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0010g0034others(2): Show | 5 | HG01258.hp1 HG01981.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(34): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0016g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(35): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0056g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(36): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(37): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0042g0029a0001c0001t0077g0012 | 2 | HG03516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(40): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(33): Show |
1 | a0001c0005t0025g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(44): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(34): Show |
3 | a0001c0001t0008g0013a0001c0012t0045g0035a0004c0011t0001g0178 | 3 | HG03209.hp1 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1021-6724_1021-672 others(45): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641932
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0008g0008 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(48): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641932 | |||||
| chr7:45641933
|
A | AAAAAAAA others(3): Show |
17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(14): Show | 18 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1021-6728_1021-672 others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45641933 | |||||
| chr7:45641946
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1021-6724_1021-672 others(32): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641946 | ||||||
| chr7:45641947
|
T | A | 18 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(15): Show | 19 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1021-6723T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45641947 | ||||||
| chr7:45642064
|
C | G | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1021-6606C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642064 | ||||||
| chr7:45642118
|
T | C | 3 | a0001c0001t0002g0216a0001c0001t0002g0221a0001c0001t0073g0207 | 3 | NA19010.hp1 NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1021-6552T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642118 | ||||||
| chr7:45642337
|
T | C | 15 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(12): Show | 15 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021-6333T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642337 | ||||||
| chr7:45642356
|
A | G | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-6314A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642356 | ||||||
| chr7:45642537
|
C | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-6133C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642537 | ||||||
| chr7:45642600
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1021-6070G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642600 | ||||||
| chr7:45642652
|
C | T | 7 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1021-6018C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642652 | ||||||
| chr7:45642834
|
A | C | 1 | a0001c0002t0003g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1021-5836A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642834 | ||||||
| chr7:45642866
|
G | A | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(14): Show | 18 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1021-5804G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642866 | ||||||
| chr7:45642988
|
G | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1021-5682G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45642988 | ||||||
| chr7:45643038
|
G | A | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-5632G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643038 | ||||||
| chr7:45643054
|
G | C | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(14): Show | 18 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1021-5616G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643054 | ||||||
| chr7:45643113
|
C | CT | 5 | a0001c0001t0001g0144a0001c0001t0005g0194a0001c0001t0070g0065others(2): Show | 5 | HG01255.hp2 HG03209.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-5539dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45643113 | |||||
| chr7:45643113
|
C | CTT | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-5540_1021-553 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45643113 | |||||
| chr7:45643113
|
C | CTTT | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0008g0013others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-5541_1021-553 others(7): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45643113 | |||||
| chr7:45643113
|
CT | C | 14 | a0001c0001t0001g0069a0001c0001t0001g0103a0001c0001t0002g0016others(11): Show | 14 | HG02155.hp1 HG02155.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021-5539delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45643113 | |||||
| chr7:45643270
|
AT | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(156): Show | 162 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1021-5390delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr7 | 45643270 | |||||
| chr7:45643528
|
A | G | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-5142A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643528 | ||||||
| chr7:45643622
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1021-5048T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643622 | ||||||
| chr7:45643714
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-4956G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643714 | ||||||
| chr7:45643855
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021-4815T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643855 | ||||||
| chr7:45643872
|
C | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021-4798C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643872 | ||||||
| chr7:45643884
|
A | G | 22 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.1021-4786A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643884 | ||||||
| chr7:45643912
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1021-4758G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643912 | ||||||
| chr7:45643956
|
T | A | 2 | a0001c0001t0006g0049a0001c0001t0034g0047 | 2 | NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1021-4714T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45643956 | ||||||
| chr7:45644050
|
A | G | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1021-4620A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644050 | ||||||
| chr7:45644205
|
A | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(155): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1021-4465A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644205 | ||||||
| chr7:45644318
|
C | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0039g0150others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-4352C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644318 | ||||||
| chr7:45644336
|
C | A | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(14): Show | 17 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1021-4334C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644336 | ||||||
| chr7:45644720
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1021-3950T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644720 | ||||||
| chr7:45644728
|
G | C | 3 | a0001c0001t0002g0089a0001c0001t0005g0001a0001c0001t0005g0088 | 4 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-3942G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644728 | ||||||
| chr7:45644802
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1021-3868C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644802 | ||||||
| chr7:45644832
|
A | T | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG02258.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1021-3838A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644832 | ||||||
| chr7:45644836
|
A | G | 1 | a0001c0006t0023g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1021-3834A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644836 | ||||||
| chr7:45644945
|
G | A | 51 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0016others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1021-3725G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644945 | ||||||
| chr7:45644969
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0010g0034others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-3701C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45644969 | ||||||
| chr7:45645323
|
T | C | 1 | a0001c0001t0069g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1021-3347T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645323 | ||||||
| chr7:45645330
|
C | G | 22 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0087others(19): Show | 23 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1021-3340C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645330 | ||||||
| chr7:45645375
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0215a0001c0001t0001g0228others(58): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1021-3295G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645375 | ||||||
| chr7:45645383
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1021-3287C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645383 | ||||||
| chr7:45645491
|
C | T | 1 | a0001c0002t0003g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1021-3179C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645491 | ||||||
| chr7:45645559
|
C | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01884.hp2 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1021-3111C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645559 | ||||||
| chr7:45645597
|
G | A | 39 | a0001c0001t0001g0228a0001c0001t0001g0238a0001c0001t0001g0240others(36): Show | 40 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1021-3073G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645597 | ||||||
| chr7:45645638
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1021-3032C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645638 | ||||||
| chr7:45645651
|
G | A | 130 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0030others(127): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1021-3019G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645651 | ||||||
| chr7:45645943
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1021-2727C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45645943 | ||||||
| chr7:45646091
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1021-2579C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646091 | ||||||
| chr7:45646158
|
A | G | 15 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0087others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1021-2512A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646158 | ||||||
| chr7:45646320
|
G | A | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1021-2350G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646320 | ||||||
| chr7:45646344
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0185others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-2326C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646344 | ||||||
| chr7:45646474
|
C | G | 31 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0075others(28): Show | 32 | HG00280.hp2 HG01099.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1021-2196C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646474 | ||||||
| chr7:45646698
|
T | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1021-1972T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646698 | ||||||
| chr7:45646954
|
G | A | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00738.hp2 HG01167.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1021-1716G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45646954 | ||||||
| chr7:45647150
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0005g0194 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1021-1520C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647150 | ||||||
| chr7:45647217
|
C | G | 11 | a0001c0002t0003g0116a0001c0002t0003g0119a0001c0002t0003g0120others(8): Show | 11 | HG00140.hp1 HG00642.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021-1453C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647217 | ||||||
| chr7:45647290
|
G | C | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1021-1380G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647290 | ||||||
| chr7:45647387
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1021-1283A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647387 | ||||||
| chr7:45647455
|
G | A | 3 | a0001c0001t0002g0089a0001c0001t0005g0001a0001c0001t0005g0088 | 4 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-1215G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647455 | ||||||
| chr7:45647912
|
G | C | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1021-758G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647912 | ||||||
| chr7:45647979
|
C | T | 1 | a0001c0002t0003g0131 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1021-691C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45647979 | ||||||
| chr7:45648068
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(126): Show | 132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1021-602T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648068 | ||||||
| chr7:45648152
|
T | C | 3 | a0001c0001t0010g0025a0001c0001t0043g0146a0001c0001t0044g0118 | 3 | HG00738.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1021-518T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648152 | ||||||
| chr7:45648286
|
G | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1021-384G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648286 | ||||||
| chr7:45648328
|
G | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0185others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1021-342G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648328 | ||||||
| chr7:45648383
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-287A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648383 | ||||||
| chr7:45648393
|
C | T | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-277C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648393 | ||||||
| chr7:45648474
|
A | G | 12 | a0001c0001t0002g0075a0001c0001t0002g0187a0001c0001t0002g0188others(9): Show | 12 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1021-196A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648474 | ||||||
| chr7:45648571
|
G | A | 1 | a0001c0002t0003g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1021-99G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648571 | ||||||
| chr7:45648634
|
G | A | 52 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0030others(49): Show | 52 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1021-36G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648634 | ||||||
| chr7:45648665
|
T | C | 1 | a0001c0001t0028g0133 | 1 | HG01496.hp1 | splice_region_variant&intron_variant | LOW | c.1021-5T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 4/19 | chr7 | 45648665 | ||||||
| chr7:45648976
|
A | G | 31 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0075others(28): Show | 32 | HG00280.hp2 HG01099.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1148+179A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45648976 | ||||||
| chr7:45648994
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1148+197C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45648994 | ||||||
| chr7:45649013
|
A | G | 26 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.1148+216A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45649013 | ||||||
| chr7:45649017
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1148+220C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45649017 | ||||||
| chr7:45649409
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1148+612T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45649409 | ||||||
| chr7:45649547
|
A | G | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1148+750A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45649547 | ||||||
| chr7:45649713
|
G | C | 2 | a0001c0001t0006g0049a0001c0001t0034g0047 | 2 | NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1148+916G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45649713 | ||||||
| chr7:45650131
|
A | G | 4 | a0001c0002t0003g0195a0001c0002t0011g0112a0001c0002t0011g0142others(1): Show | 4 | HG01433.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+1334A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650131 | ||||||
| chr7:45650206
|
A | C | 2 | a0001c0001t0001g0237a0001c0001t0005g0194 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1148+1409A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650206 | ||||||
| chr7:45650282
|
C | T | 5 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(2): Show | 5 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+1485C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650282 | ||||||
| chr7:45650330
|
G | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0030others(80): Show | 84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1148+1533G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650330 | ||||||
| chr7:45650395
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1148+1598C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650395 | ||||||
| chr7:45650412
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0228others(34): Show | 39 | HG00609.hp2 HG00642.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1148+1615C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650412 | ||||||
| chr7:45650502
|
C | T | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1148+1705C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650502 | ||||||
| chr7:45650753
|
C | T | 15 | a0001c0001t0002g0075a0001c0001t0002g0187a0001c0001t0002g0188others(12): Show | 15 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1148+1956C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650753 | ||||||
| chr7:45650810
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+2013C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45650810 | ||||||
| chr7:45651072
|
G | A | 4 | a0001c0001t0002g0063a0001c0001t0042g0029a0001c0006t0023g0078others(1): Show | 4 | HG02970.hp1 HG03516.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+2275G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651072 | ||||||
| chr7:45651205
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1148+2408C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651205 | ||||||
| chr7:45651304
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1148+2507C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651304 | ||||||
| chr7:45651460
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0156a0001c0001t0001g0160others(12): Show | 15 | HG01261.hp1 HG01928.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1148+2663T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651460 | ||||||
| chr7:45651513
|
A | G | 1 | a0001c0001t0032g0040 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1148+2716A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651513 | ||||||
| chr7:45651528
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1148+2731A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651528 | ||||||
| chr7:45651529
|
G | A | 16 | a0001c0001t0002g0075a0001c0001t0002g0187a0001c0001t0002g0188others(13): Show | 16 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1148+2732G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651529 | ||||||
| chr7:45651540
|
C | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG01167.hp1 HG02027.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+2743C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651540 | ||||||
| chr7:45651595
|
A | T | 1 | a0001c0001t0015g0048 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1148+2798A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651595 | ||||||
| chr7:45651747
|
C | T | 3 | a0001c0001t0010g0025a0001c0001t0043g0146a0001c0001t0044g0118 | 3 | HG00738.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1148+2950C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651747 | ||||||
| chr7:45651785
|
C | G | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1148+2988C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651785 | ||||||
| chr7:45651869
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0016g0235 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1148+3072T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651869 | ||||||
| chr7:45651920
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1148+3123T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45651920 | ||||||
| chr7:45652068
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+3271A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652068 | ||||||
| chr7:45652274
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0185others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+3477G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652274 | ||||||
| chr7:45652290
|
T | C | 3 | a0002c0003t0007g0031a0002c0003t0007g0032a0002c0003t0007g0033 | 3 | HG01257.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1148+3493T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652290 | ||||||
| chr7:45652332
|
T | G | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1148+3535T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652332 | ||||||
| chr7:45652341
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0185others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+3544C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652341 | ||||||
| chr7:45652542
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0197a0001c0001t0001g0228others(30): Show | 35 | HG00609.hp2 HG00642.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1148+3745G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652542 | ||||||
| chr7:45652621
|
C | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(10): Show | 13 | HG00738.hp2 HG01167.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1148+3824C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652621 | ||||||
| chr7:45652759
|
G | A | 1 | a0001c0001t0004g0205 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1148+3962G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652759 | ||||||
| chr7:45652905
|
C | T | 3 | a0001c0001t0053g0236a0001c0001t0068g0180a0001c0001t0069g0239 | 3 | HG02258.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1148+4108C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45652905 | ||||||
| chr7:45653040
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG00423.hp1 HG01167.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+4243C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653040 | ||||||
| chr7:45653192
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1148+4395C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653192 | ||||||
| chr7:45653249
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+4452C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653249 | ||||||
| chr7:45653484
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1149-4243G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653484 | ||||||
| chr7:45653513
|
G | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149-4214G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653513 | ||||||
| chr7:45653662
|
G | T | 2 | a0001c0001t0004g0198a0001c0001t0004g0199 | 2 | NA18975.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1149-4065G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653662 | ||||||
| chr7:45653729
|
A | G | 15 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0087others(12): Show | 16 | HG00280.hp2 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149-3998A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653729 | ||||||
| chr7:45653763
|
G | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(121): Show | 127 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1149-3964G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653763 | ||||||
| chr7:45653968
|
C | G | 12 | a0001c0001t0002g0075a0001c0001t0002g0187a0001c0001t0002g0188others(9): Show | 12 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-3759C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45653968 | ||||||
| chr7:45654035
|
C | G | 1 | a0001c0001t0008g0011 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1149-3692C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654035 | ||||||
| chr7:45654121
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0024g0206a0001c0001t0024g0222others(2): Show | 6 | NA18954.hp1 NA18957.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-3606A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654121 | ||||||
| chr7:45654168
|
A | G | 7 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(4): Show | 7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-3559A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654168 | ||||||
| chr7:45654212
|
T | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(125): Show | 131 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1149-3515T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654212 | ||||||
| chr7:45654264
|
G | A | 82 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0030others(79): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1149-3463G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654264 | ||||||
| chr7:45654388
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0027others(133): Show | 139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1149-3339A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654388 | ||||||
| chr7:45654479
|
A | G | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG00423.hp1 HG01167.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-3248A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654479 | ||||||
| chr7:45654600
|
G | T | 1 | a0001c0001t0006g0059 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1149-3127G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654600 | ||||||
| chr7:45654639
|
C | T | 1 | a0001c0001t0004g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1149-3088C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654639 | ||||||
| chr7:45654664
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0070g0065 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1149-3063C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654664 | ||||||
| chr7:45654925
|
C | T | 2 | a0001c0002t0003g0117a0001c0002t0003g0181 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-2802C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654925 | ||||||
| chr7:45654942
|
GCCCTT | G | 6 | a0001c0001t0001g0023a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-2781_1149-277 others(9): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr7 | 45654942 | |||||
| chr7:45654988
|
G | A | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00423.hp1 HG01167.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-2739G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45654988 | ||||||
| chr7:45655044
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1149-2683A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655044 | ||||||
| chr7:45655256
|
C | T | 1 | a0001c0001t0074g0224 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1149-2471C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655256 | ||||||
| chr7:45655327
|
T | C | 14 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(11): Show | 14 | HG00423.hp1 HG00738.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1149-2400T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655327 | ||||||
| chr7:45655552
|
G | A | 4 | a0001c0002t0003g0015a0001c0002t0003g0021a0001c0002t0003g0081others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-2175G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655552 | ||||||
| chr7:45655556
|
T | C | 17 | a0001c0001t0004g0273a0001c0001t0006g0044a0001c0001t0006g0049others(14): Show | 17 | HG00423.hp1 HG00423.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1149-2171T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655556 | ||||||
| chr7:45655625
|
C | A | 1 | a0001c0016t0001g0138 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1149-2102C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655625 | ||||||
| chr7:45655732
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0091others(85): Show | 89 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1149-1995A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655732 | ||||||
| chr7:45655797
|
CCGTGCCA others(3): Show |
C | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1149-1929_1149-192 others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655797 | ||||||
| chr7:45655808
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1149-1919A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655808 | ||||||
| chr7:45655838
|
T | C | 55 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0068others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1149-1889T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655838 | ||||||
| chr7:45655855
|
G | A | 9 | a0001c0001t0002g0073a0001c0001t0006g0051a0001c0001t0006g0053others(6): Show | 9 | HG01981.hp1 HG02027.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149-1872G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655855 | ||||||
| chr7:45655869
|
A | G | 28 | a0001c0001t0001g0152a0001c0001t0001g0179a0001c0001t0001g0212others(25): Show | 28 | HG00280.hp2 HG00423.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1149-1858A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655869 | ||||||
| chr7:45655873
|
T | G | 25 | a0001c0001t0001g0152a0001c0001t0001g0179a0001c0001t0001g0212others(22): Show | 26 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1149-1854T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655873 | ||||||
| chr7:45655888
|
G | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0077a0001c0001t0016g0098others(6): Show | 9 | HG01884.hp2 HG02723.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149-1839G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655888 | ||||||
| chr7:45655984
|
G | A | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1149-1743G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45655984 | ||||||
| chr7:45656014
|
A | G | 6 | a0001c0001t0001g0249a0001c0001t0015g0041a0001c0001t0053g0236others(3): Show | 6 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-1713A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656014 | ||||||
| chr7:45656015
|
T | C | 5 | a0001c0001t0001g0249a0001c0001t0015g0041a0001c0013t0001g0223others(2): Show | 5 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-1712T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656015 | ||||||
| chr7:45656023
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1149-1704C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656023 | ||||||
| chr7:45656188
|
A | G | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1149-1539A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656188 | ||||||
| chr7:45656228
|
G | A | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149-1499G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656228 | ||||||
| chr7:45656235
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1149-1492G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656235 | ||||||
| chr7:45656281
|
C | A | 2 | a0001c0002t0003g0268a0001c0002t0003g0269 | 2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1149-1446C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656281 | ||||||
| chr7:45656298
|
G | A | 2 | a0001c0001t0006g0059a0001c0009t0006g0061 | 2 | HG01981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1149-1429G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656298 | ||||||
| chr7:45656302
|
CA | C | 18 | a0001c0001t0002g0062a0001c0001t0008g0008a0001c0001t0008g0009others(15): Show | 18 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1149-1411delA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr7 | 45656302 | |||||
| chr7:45656666
|
G | A | 1 | a0001c0002t0003g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1149-1061G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656666 | ||||||
| chr7:45656701
|
G | A | 4 | a0001c0001t0001g0249a0001c0001t0015g0041a0001c0013t0001g0223others(1): Show | 4 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-1026G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656701 | ||||||
| chr7:45656707
|
C | T | 1 | a0001c0008t0001g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1149-1020C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656707 | ||||||
| chr7:45656802
|
A | G | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1149-925A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656802 | ||||||
| chr7:45656804
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1149-923C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656804 | ||||||
| chr7:45656812
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1149-915C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656812 | ||||||
| chr7:45656824
|
C | A | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1149-903C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656824 | ||||||
| chr7:45656882
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1149-845C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656882 | ||||||
| chr7:45656952
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0077 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1149-775G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45656952 | ||||||
| chr7:45657469
|
A | T | 3 | a0001c0001t0001g0030a0001c0002t0026g0005a0001c0002t0026g0264 | 3 | HG01106.hp1 HG01109.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1149-258A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45657469 | ||||||
| chr7:45657505
|
A | C | 1 | a0001c0002t0062g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1149-222A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45657505 | ||||||
| chr7:45657596
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1149-131C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45657596 | ||||||
| chr7:45657696
|
C | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(166): Show | 171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1149-31C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45657696 | ||||||
| chr7:45657698
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(231): Show | 237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1149-29T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 5/19 | chr7 | 45657698 | ||||||
| chr7:45658155
|
C | T | 1 | a0001c0001t0005g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1307+270C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658155 | ||||||
| chr7:45658298
|
A | C | 1 | a0001c0002t0011g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1307+413A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658298 | ||||||
| chr7:45658398
|
A | G | 14 | a0001c0001t0002g0170a0001c0001t0008g0008a0001c0001t0008g0009others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1307+513A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658398 | ||||||
| chr7:45658467
|
A | G | 4 | a0001c0001t0002g0097a0001c0001t0002g0135a0001c0001t0002g0155others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+582A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658467 | ||||||
| chr7:45658478
|
G | T | 1 | a0001c0001t0008g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1307+593G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658478 | ||||||
| chr7:45658581
|
G | A | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1307+696G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658581 | ||||||
| chr7:45658654
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(173): Show | 178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1307+769T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658654 | ||||||
| chr7:45658817
|
C | A | 1 | a0001c0001t0013g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1307+932C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658817 | ||||||
| chr7:45658978
|
T | C | 1 | a0001c0001t0006g0051 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1308-1064T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45658978 | ||||||
| chr7:45659069
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(268): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1308-973A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659069 | ||||||
| chr7:45659097
|
C | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1308-945C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659097 | ||||||
| chr7:45659213
|
A | G | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1308-829A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659213 | ||||||
| chr7:45659336
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1308-706C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659336 | ||||||
| chr7:45659382
|
G | T | 68 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1308-660G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659382 | ||||||
| chr7:45659770
|
T | C | 17 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(14): Show | 17 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.1308-272T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659770 | ||||||
| chr7:45659771
|
CTT | C | 40 | a0001c0001t0001g0271a0001c0001t0043g0146a0001c0001t0044g0118others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1308-270_1308-269d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659771 | ||||||
| chr7:45659834
|
T | C | 2 | a0001c0002t0003g0195a0001c0002t0011g0014 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1308-208T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659834 | ||||||
| chr7:45659835
|
G | T | 2 | a0001c0002t0003g0195a0001c0002t0011g0014 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1308-207G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659835 | ||||||
| chr7:45659892
|
C | T | 1 | a0001c0002t0003g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1308-150C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659892 | ||||||
| chr7:45659893
|
G | A | 16 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(13): Show | 16 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1308-149G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659893 | ||||||
| chr7:45659984
|
G | C | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1308-58G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 6/19 | chr7 | 45659984 | ||||||
| chr7:45660191
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | splice_region_variant&intron_variant | LOW | c.1449+8C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660191 | ||||||
| chr7:45660495
|
G | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02258.hp1 HG03471.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+312G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660495 | ||||||
| chr7:45660503
|
G | T | 1 | a0001c0001t0002g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1449+320G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660503 | ||||||
| chr7:45660699
|
G | A | 1 | a0001c0001t0077g0012 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1449+516G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660699 | ||||||
| chr7:45660720
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1449+537G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660720 | ||||||
| chr7:45660746
|
G | T | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+563G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660746 | ||||||
| chr7:45660855
|
G | A | 1 | a0001c0001t0044g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1449+672G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660855 | ||||||
| chr7:45660858
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(89): Show | 94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1449+675C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660858 | ||||||
| chr7:45660887
|
T | G | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1449+704T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45660887 | ||||||
| chr7:45661030
|
G | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1449+847G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661030 | ||||||
| chr7:45661064
|
C | T | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1449+881C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661064 | ||||||
| chr7:45661389
|
C | T | 2 | a0001c0001t0010g0025a0001c0001t0046g0072 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1450-670C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661389 | ||||||
| chr7:45661549
|
T | G | 3 | a0002c0003t0007g0031a0002c0003t0007g0032a0002c0003t0007g0033 | 3 | HG01257.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1450-510T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661549 | ||||||
| chr7:45661635
|
C | G | 18 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(15): Show | 18 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1450-424C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661635 | ||||||
| chr7:45661716
|
A | C | 1 | a0001c0002t0014g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1450-343A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661716 | ||||||
| chr7:45661717
|
C | CG | 4 | a0001c0001t0005g0231a0001c0001t0021g0045a0001c0001t0021g0060others(1): Show | 4 | HG02897.hp1 NA18994.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-338dupG | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr7 | 45661717 | |||||
| chr7:45661717
|
C | G | 1 | a0001c0002t0014g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1450-342C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45661717 | ||||||
| chr7:45662014
|
G | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1450-45G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45662014 | ||||||
| chr7:45662014
|
G | T | 7 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450-45G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45662014 | ||||||
| chr7:45662054
|
G | T | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
splice_region_variant&intron_variant | LOW | c.1450-5G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 7/19 | chr7 | 45662054 | ||||||
| chr7:45662623
|
T | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1605+409T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45662623 | ||||||
| chr7:45662782
|
G | A | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+568G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45662782 | ||||||
| chr7:45663082
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1605+868G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663082 | ||||||
| chr7:45663203
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1605+989C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663203 | ||||||
| chr7:45663310
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1605+1096C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663310 | ||||||
| chr7:45663363
|
A | G | 4 | a0001c0001t0001g0249a0001c0001t0015g0041a0001c0013t0001g0223others(1): Show | 4 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605+1149A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663363 | ||||||
| chr7:45663483
|
G | A | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1605+1269G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663483 | ||||||
| chr7:45663497
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1605+1283G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663497 | ||||||
| chr7:45663516
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1605+1302G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663516 | ||||||
| chr7:45663602
|
C | T | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1605+1388C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663602 | ||||||
| chr7:45663715
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1605+1501A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663715 | ||||||
| chr7:45663744
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0077 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1605+1530G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663744 | ||||||
| chr7:45663818
|
C | CA | 10 | a0001c0001t0002g0170a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1605+1616dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45663818 | |||||
| chr7:45663899
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(103): Show | 108 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1605+1685A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663899 | ||||||
| chr7:45663941
|
C | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1605+1727C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45663941 | ||||||
| chr7:45664159
|
C | A | 7 | a0001c0001t0002g0170a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+1945C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664159 | ||||||
| chr7:45664236
|
G | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0075a0001c0001t0002g0077 | 3 | HG01884.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1605+2022G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664236 | ||||||
| chr7:45664372
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(97): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1605+2158G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664372 | ||||||
| chr7:45664690
|
C | T | 39 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(36): Show | 39 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1605+2476C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664690 | ||||||
| chr7:45664810
|
C | T | 1 | a0001c0002t0003g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1605+2596C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664810 | ||||||
| chr7:45664832
|
A | G | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+2618A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664832 | ||||||
| chr7:45664869
|
C | T | 12 | a0001c0001t0001g0093a0001c0001t0001g0104a0001c0001t0001g0106others(9): Show | 12 | HG00738.hp2 HG02056.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1605+2655C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664869 | ||||||
| chr7:45664891
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1605+2677G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45664891 | ||||||
| chr7:45665026
|
C | T | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1605+2812C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665026 | ||||||
| chr7:45665095
|
G | C | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+2881G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665095 | ||||||
| chr7:45665237
|
C | G | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1605+3023C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665237 | ||||||
| chr7:45665418
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(213): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1605+3204A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665418 | ||||||
| chr7:45665526
|
T | C | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1605+3312T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665526 | ||||||
| chr7:45665607
|
A | T | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1605+3393A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665607 | ||||||
| chr7:45665750
|
A | G | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1605+3536A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665750 | ||||||
| chr7:45665829
|
G | A | 40 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1605+3615G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665829 | ||||||
| chr7:45665861
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(97): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1605+3647A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665861 | ||||||
| chr7:45665925
|
T | C | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1605+3711T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45665925 | ||||||
| chr7:45666061
|
A | G | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+3847A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666061 | ||||||
| chr7:45666088
|
G | C | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1605+3874G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666088 | ||||||
| chr7:45666149
|
A | G | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1605+3935A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666149 | ||||||
| chr7:45666242
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+4028C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666242 | ||||||
| chr7:45666252
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+4038A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666252 | ||||||
| chr7:45666258
|
T | C | 9 | a0001c0001t0002g0170a0001c0001t0008g0008a0001c0001t0008g0009others(6): Show | 9 | HG00140.hp2 HG00673.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1605+4044T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666258 | ||||||
| chr7:45666281
|
C | T | 38 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4067C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666281 | ||||||
| chr7:45666304
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1605+4090G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666304 | ||||||
| chr7:45666339
|
A | T | 1 | a0001c0001t0071g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1605+4125A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666339 | ||||||
| chr7:45666365
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1605+4151T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666365 | ||||||
| chr7:45666379
|
T | C | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+4165T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666379 | ||||||
| chr7:45666404
|
C | T | 38 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1605+4190C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666404 | ||||||
| chr7:45666405
|
G | A | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1605+4191G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666405 | ||||||
| chr7:45666405
|
G | C | 1 | a0001c0001t0012g0214 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1605+4191G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666405 | ||||||
| chr7:45666589
|
C | T | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+4375C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666589 | ||||||
| chr7:45666670
|
A | G | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1605+4456A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666670 | ||||||
| chr7:45666697
|
C | T | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1605+4483C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666697 | ||||||
| chr7:45666716
|
A | G | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1605+4502A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666716 | ||||||
| chr7:45666904
|
T | C | 20 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(17): Show | 20 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1605+4690T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666904 | ||||||
| chr7:45666906
|
T | G | 20 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(17): Show | 20 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1605+4692T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45666906 | ||||||
| chr7:45667022
|
A | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(94): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1605+4808A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667022 | ||||||
| chr7:45667092
|
A | G | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1605+4878A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667092 | ||||||
| chr7:45667093
|
C | A | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1605+4879C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667093 | ||||||
| chr7:45667094
|
T | A | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1605+4880T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667094 | ||||||
| chr7:45667144
|
T | G | 7 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.1605+4930T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667144 | ||||||
| chr7:45667328
|
G | A | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG00423.hp1 HG01167.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1605+5114G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667328 | ||||||
| chr7:45667439
|
A | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1605+5225A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667439 | ||||||
| chr7:45667661
|
G | A | 1 | a0001c0002t0014g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1605+5447G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667661 | ||||||
| chr7:45667667
|
A | G | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1605+5453A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667667 | ||||||
| chr7:45667779
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(132): Show | 138 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1605+5565A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45667779 | ||||||
| chr7:45668099
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1605+5885G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668099 | ||||||
| chr7:45668160
|
A | G | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1605+5946A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668160 | ||||||
| chr7:45668185
|
G | C | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1605+5971G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668185 | ||||||
| chr7:45668189
|
G | A | 2 | a0001c0001t0004g0273a0001c0001t0066g0024 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1605+5975G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668189 | ||||||
| chr7:45668223
|
A | G | 3 | a0001c0001t0002g0063a0001c0001t0010g0025a0001c0001t0070g0065 | 3 | HG01891.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1605+6009A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668223 | ||||||
| chr7:45668347
|
G | C | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1605+6133G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668347 | ||||||
| chr7:45668402
|
G | A | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1605+6188G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668402 | ||||||
| chr7:45668402
|
G | T | 1 | a0001c0002t0003g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1605+6188G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668402 | ||||||
| chr7:45668510
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1605+6296G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668510 | ||||||
| chr7:45668541
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1605+6327C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668541 | ||||||
| chr7:45668681
|
A | G | 2 | a0001c0002t0003g0006a0001c0002t0003g0195 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1605+6467A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668681 | ||||||
| chr7:45668704
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1605+6490G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668704 | ||||||
| chr7:45668750
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1605+6536C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668750 | ||||||
| chr7:45668751
|
G | A | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1605+6537G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668751 | ||||||
| chr7:45668880
|
T | C | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1605+6666T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668880 | ||||||
| chr7:45668919
|
G | T | 1 | a0001c0002t0003g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1605+6705G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45668919 | ||||||
| chr7:45669012
|
C | G | 1 | a0001c0001t0044g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1605+6798C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669012 | ||||||
| chr7:45669106
|
A | G | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1605+6892A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669106 | ||||||
| chr7:45669261
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1605+7047A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669261 | ||||||
| chr7:45669512
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1605+7298A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669512 | ||||||
| chr7:45669736
|
A | G | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+7522A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669736 | ||||||
| chr7:45669805
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(98): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1605+7591A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45669805 | ||||||
| chr7:45670028
|
G | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(271): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1605+7814G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670028 | ||||||
| chr7:45670086
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1606-7783C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670086 | ||||||
| chr7:45670275
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(271): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1606-7594G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670275 | ||||||
| chr7:45670317
|
C | T | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1606-7552C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670317 | ||||||
| chr7:45670408
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1606-7461G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670408 | ||||||
| chr7:45670462
|
C | G | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1606-7407C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670462 | ||||||
| chr7:45670528
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1606-7341C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670528 | ||||||
| chr7:45670636
|
G | A | 4 | a0001c0001t0002g0274a0001c0001t0029g0203a0001c0001t0029g0204others(1): Show | 4 | HG02027.hp2 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1606-7233G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670636 | ||||||
| chr7:45670669
|
G | A | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1606-7200G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670669 | ||||||
| chr7:45670683
|
A | G | 40 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1606-7186A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670683 | ||||||
| chr7:45670717
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1606-7152C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45670717 | ||||||
| chr7:45671274
|
T | A | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1606-6595T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45671274 | ||||||
| chr7:45671275
|
T | C | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1606-6594T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45671275 | ||||||
| chr7:45671276
|
T | A | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1606-6593T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45671276 | ||||||
| chr7:45671360
|
A | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1606-6509A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45671360 | ||||||
| chr7:45671574
|
C | G | 1 | a0001c0002t0003g0248 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1606-6295C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45671574 | ||||||
| chr7:45672085
|
T | C | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1606-5784T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672085 | ||||||
| chr7:45672104
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1606-5765T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672104 | ||||||
| chr7:45672182
|
C | A | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1606-5687C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672182 | ||||||
| chr7:45672298
|
A | G | 1 | a0001c0016t0001g0138 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1606-5571A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672298 | ||||||
| chr7:45672389
|
T | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1606-5480T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672389 | ||||||
| chr7:45672444
|
G | GT | 40 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1606-5424dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45672444 | |||||
| chr7:45672487
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1606-5382C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672487 | ||||||
| chr7:45672769
|
T | C | 1 | a0001c0007t0005g0233 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1606-5100T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672769 | ||||||
| chr7:45672797
|
C | T | 66 | a0001c0001t0001g0271a0001c0001t0004g0067a0001c0001t0004g0147others(63): Show | 66 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1606-5072C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672797 | ||||||
| chr7:45672859
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1606-5010G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45672859 | ||||||
| chr7:45673118
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1606-4751C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673118 | ||||||
| chr7:45673196
|
A | AT | 39 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(36): Show | 39 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1606-4665dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673196 | |||||
| chr7:45673377
|
C | T | 17 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(14): Show | 17 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.1606-4492C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673377 | ||||||
| chr7:45673462
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(170): Show | 175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1606-4407A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673462 | ||||||
| chr7:45673692
|
T | A | 1 | a0001c0002t0011g0167 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1606-4177T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673692 | ||||||
| chr7:45673717
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(169): Show | 174 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1606-4152T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673717 | ||||||
| chr7:45673751
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1606-4118T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673751 | ||||||
| chr7:45673964
|
C | CAT | 13 | a0001c0001t0001g0271a0001c0001t0005g0182a0001c0001t0009g0083others(10): Show | 13 | HG01071.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1606-3862_1606-386 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
C | CATATATA others(7): Show |
1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1606-3874_1606-386 others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CAT | C | 23 | a0001c0001t0009g0080a0001c0001t0009g0085a0001c0001t0009g0086others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.1606-3862_1606-386 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATAT | C | 6 | a0001c0001t0004g0205a0001c0001t0005g0230a0001c0001t0005g0231others(3): Show | 6 | HG01891.hp1 NA18612.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.1606-3864_1606-386 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATAT | C | 9 | a0001c0001t0004g0198a0001c0001t0005g0001a0001c0001t0005g0088others(6): Show | 10 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1606-3866_1606-386 others(10): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(1): Show |
C | 15 | a0001c0001t0004g0199a0001c0001t0004g0273a0001c0001t0005g0158others(12): Show | 15 | HG00423.hp2 HG01256.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1606-3868_1606-386 others(12): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(3): Show |
C | 8 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0006g0049others(5): Show | 8 | HG00673.hp2 HG02809.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1606-3870_1606-386 others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(7): Show |
C | 9 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1606-3874_1606-386 others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(9): Show |
C | 3 | a0001c0001t0002g0132a0001c0001t0060g0019a0001c0008t0001g0244 | 3 | HG00423.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1606-3876_1606-386 others(20): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(11): Show |
C | 6 | a0001c0001t0001g0257a0001c0001t0016g0028a0001c0001t0016g0098others(3): Show | 6 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606-3878_1606-386 others(22): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(13): Show |
C | 3 | a0001c0001t0001g0107a0001c0001t0001g0252a0001c0001t0051g0254 | 3 | HG01175.hp1 HG03239.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1606-3880_1606-386 others(24): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(15): Show |
C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(98): Show | 103 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1606-3882_1606-386 others(26): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673964
|
CATATATA others(17): Show |
C | 62 | a0001c0001t0001g0030a0001c0001t0002g0016a0001c0001t0002g0022others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1606-3884_1606-386 others(28): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45673964 | |||||
| chr7:45673997
|
A | G | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1606-3872A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45673997 | ||||||
| chr7:45674172
|
T | A | 1 | a0001c0001t0066g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1606-3697T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674172 | ||||||
| chr7:45674401
|
C | T | 38 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1606-3468C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674401 | ||||||
| chr7:45674438
|
G | T | 1 | a0001c0001t0022g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1606-3431G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674438 | ||||||
| chr7:45674479
|
A | G | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1606-3390A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674479 | ||||||
| chr7:45674506
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | NA18939.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1606-3363T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674506 | ||||||
| chr7:45674651
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1606-3218C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674651 | ||||||
| chr7:45674664
|
G | A | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1606-3205G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674664 | ||||||
| chr7:45674698
|
G | A | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1606-3171G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674698 | ||||||
| chr7:45674842
|
G | A | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1606-3027G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45674842 | ||||||
| chr7:45675016
|
T | C | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1606-2853T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675016 | ||||||
| chr7:45675047
|
T | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1606-2822T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675047 | ||||||
| chr7:45675067
|
T | C | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1606-2802T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675067 | ||||||
| chr7:45675095
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1606-2774G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675095 | ||||||
| chr7:45675241
|
A | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1606-2628A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675241 | ||||||
| chr7:45675290
|
A | C | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1606-2579A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675290 | ||||||
| chr7:45675302
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1606-2567T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675302 | ||||||
| chr7:45675351
|
T | C | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1606-2518T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675351 | ||||||
| chr7:45675375
|
T | C | 40 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1606-2494T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675375 | ||||||
| chr7:45675468
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(165): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1606-2401T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45675468 | ||||||
| chr7:45676048
|
G | GT | 88 | a0001c0001t0001g0215a0001c0001t0002g0016a0001c0001t0002g0022others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1606-1809dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676048 | |||||
| chr7:45676050
|
T | TTTG | 19 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(16): Show | 19 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1606-1817_1606-181 others(7): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676050 | |||||
| chr7:45676053
|
T | G | 40 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1606-1816T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676053 | ||||||
| chr7:45676115
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(97): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1606-1754T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676115 | ||||||
| chr7:45676168
|
T | G | 108 | a0001c0001t0001g0215a0001c0001t0002g0016a0001c0001t0002g0022others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1606-1701T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676168 | ||||||
| chr7:45676345
|
C | CT | 26 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(23): Show | 26 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.1606-1523dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676345 | |||||
| chr7:45676664
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1606-1205T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676664 | ||||||
| chr7:45676749
|
T | G | 42 | a0001c0001t0001g0271a0001c0001t0068g0180a0001c0002t0003g0006others(39): Show | 42 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1606-1120T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676749 | ||||||
| chr7:45676787
|
C | T | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1606-1082C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676787 | ||||||
| chr7:45676837
|
A | AT | 11 | a0001c0001t0002g0097a0001c0001t0002g0135a0001c0001t0002g0148others(8): Show | 11 | HG00609.hp1 HG02027.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1606-1014dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676837 | |||||
| chr7:45676837
|
AT | A | 27 | a0001c0001t0001g0242a0001c0001t0002g0022a0001c0001t0002g0073others(24): Show | 27 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1606-1014delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676837 | |||||
| chr7:45676837
|
ATT | A | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1606-1015_1606-101 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676837 | |||||
| chr7:45676990
|
A | AT | 70 | a0001c0001t0001g0215a0001c0001t0002g0016a0001c0001t0002g0022others(67): Show | 70 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.1606-873dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr7 | 45676990 | |||||
| chr7:45676992
|
T | A | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1606-877T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45676992 | ||||||
| chr7:45677063
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(112): Show | 118 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1606-806T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677063 | ||||||
| chr7:45677086
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1606-783G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677086 | ||||||
| chr7:45677304
|
T | G | 84 | a0001c0001t0001g0215a0001c0001t0002g0016a0001c0001t0002g0022others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1606-565T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677304 | ||||||
| chr7:45677314
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1606-555G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677314 | ||||||
| chr7:45677335
|
T | C | 3 | a0001c0001t0056g0241a0001c0001t0057g0010a0007c0017t0001g0153 | 3 | HG03017.hp1 HG03239.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1606-534T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677335 | ||||||
| chr7:45677351
|
C | G | 7 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.1606-518C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677351 | ||||||
| chr7:45677367
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1606-502C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677367 | ||||||
| chr7:45677567
|
C | T | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1606-302C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677567 | ||||||
| chr7:45677637
|
A | C | 3 | a0001c0001t0001g0030a0001c0002t0026g0005a0001c0002t0026g0264 | 3 | HG01106.hp1 HG01109.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1606-232A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 8/19 | chr7 | 45677637 | ||||||
| chr7:45678112
|
T | C | 19 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(16): Show | 19 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1800+49T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 9/19 | chr7 | 45678112 | ||||||
| chr7:45678311
|
T | C | 2 | a0001c0001t0001g0003a0001c0002t0050g0260 | 3 | NA18954.hp1 NA18998.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1898+48T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678311 | ||||||
| chr7:45678344
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0240a0001c0002t0026g0264others(1): Show | 4 | HG01071.hp1 HG01346.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898+81G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678344 | ||||||
| chr7:45678622
|
G | A | 38 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1898+359G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678622 | ||||||
| chr7:45678676
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(169): Show | 174 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1898+413T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678676 | ||||||
| chr7:45678687
|
C | T | 1 | a0001c0002t0003g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1898+424C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678687 | ||||||
| chr7:45678714
|
C | CA | 92 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0125others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1898+471dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr7 | 45678714 | |||||
| chr7:45678889
|
A | AAAT | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(97): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1898+644_1898+646d others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr7 | 45678889 | |||||
| chr7:45678896
|
A | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1898+633A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678896 | ||||||
| chr7:45678988
|
C | T | 1 | a0001c0001t0008g0258 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1899-721C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45678988 | ||||||
| chr7:45679041
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0092others(36): Show | 39 | HG00438.hp1 HG01261.hp1 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.1899-668G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679041 | ||||||
| chr7:45679084
|
G | A | 1 | a0001c0001t0035g0058 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1899-625G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679084 | ||||||
| chr7:45679214
|
G | A | 2 | a0001c0001t0043g0146a0001c0012t0045g0035 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1899-495G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679214 | ||||||
| chr7:45679235
|
C | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1899-474C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679235 | ||||||
| chr7:45679239
|
G | A | 2 | a0001c0002t0011g0112a0001c0002t0011g0167 | 2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1899-470G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679239 | ||||||
| chr7:45679312
|
C | T | 1 | a0001c0001t0038g0054 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1899-397C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679312 | ||||||
| chr7:45679327
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1899-382C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679327 | ||||||
| chr7:45679490
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1899-219G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679490 | ||||||
| chr7:45679657
|
C | T | 1 | a0001c0002t0003g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1899-52C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 10/19 | chr7 | 45679657 | ||||||
| chr7:45679923
|
CT | C | 18 | a0001c0001t0004g0067a0001c0001t0004g0147a0001c0001t0004g0198others(15): Show | 18 | HG00423.hp2 HG01981.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1983+132delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr7 | 45679923 | |||||
| chr7:45680110
|
G | C | 1 | a0001c0001t0008g0009 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1983+317G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680110 | ||||||
| chr7:45680276
|
C | T | 2 | a0001c0001t0001g0030a0001c0002t0026g0005 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1983+483C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680276 | ||||||
| chr7:45680328
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1983+535G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680328 | ||||||
| chr7:45680366
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1983+573A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680366 | ||||||
| chr7:45680379
|
G | A | 2 | a0001c0001t0006g0049a0001c0001t0034g0047 | 2 | NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1983+586G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680379 | ||||||
| chr7:45680404
|
T | TG | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1983+613dupG | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr7 | 45680404 | |||||
| chr7:45680429
|
T | A | 1 | a0001c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1983+636T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680429 | ||||||
| chr7:45680733
|
C | G | 1 | a0001c0006t0023g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1983+940C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680733 | ||||||
| chr7:45680879
|
T | C | 1 | a0001c0001t0066g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1983+1086T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45680879 | ||||||
| chr7:45681053
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1983+1260A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681053 | ||||||
| chr7:45681116
|
G | C | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1983+1323G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681116 | ||||||
| chr7:45681252
|
A | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(11): Show | 15 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1983+1459A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681252 | ||||||
| chr7:45681767
|
G | A | 5 | a0001c0002t0003g0015a0001c0002t0003g0017a0001c0002t0003g0021others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1983+1974G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681767 | ||||||
| chr7:45681797
|
C | T | 1 | a0001c0001t0071g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1983+2004C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681797 | ||||||
| chr7:45681849
|
G | C | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1983+2056G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681849 | ||||||
| chr7:45681935
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1983+2142G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45681935 | ||||||
| chr7:45682093
|
C | A | 1 | a0001c0001t0044g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1983+2300C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682093 | ||||||
| chr7:45682164
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1983+2371C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682164 | ||||||
| chr7:45682239
|
G | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1983+2446G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682239 | ||||||
| chr7:45682320
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(110): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1983+2527T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682320 | ||||||
| chr7:45682368
|
A | G | 1 | a0001c0001t0044g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1983+2575A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682368 | ||||||
| chr7:45682420
|
G | A | 38 | a0001c0001t0001g0271a0001c0002t0003g0006a0001c0002t0003g0015others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1984-2559G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682420 | ||||||
| chr7:45682429
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1984-2550A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682429 | ||||||
| chr7:45682590
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1984-2389G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682590 | ||||||
| chr7:45682667
|
G | A | 26 | a0001c0001t0001g0271a0001c0002t0003g0110a0001c0002t0003g0115others(23): Show | 26 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1984-2312G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682667 | ||||||
| chr7:45682722
|
C | A | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1984-2257C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682722 | ||||||
| chr7:45682952
|
T | C | 1 | a0001c0002t0014g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1984-2027T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45682952 | ||||||
| chr7:45683331
|
A | G | 65 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(62): Show | 65 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1984-1648A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683331 | ||||||
| chr7:45683385
|
C | A | 65 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(62): Show | 65 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1984-1594C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683385 | ||||||
| chr7:45683473
|
A | G | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1984-1506A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683473 | ||||||
| chr7:45683730
|
A | T | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1984-1249A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683730 | ||||||
| chr7:45683839
|
T | G | 1 | a0001c0001t0002g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1984-1140T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683839 | ||||||
| chr7:45683869
|
T | C | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1984-1110T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45683869 | ||||||
| chr7:45684053
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1984-926G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684053 | ||||||
| chr7:45684094
|
C | T | 6 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(3): Show | 6 | HG00738.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1984-885C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684094 | ||||||
| chr7:45684154
|
A | G | 2 | a0001c0002t0003g0115a0001c0002t0003g0126 | 2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1984-825A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684154 | ||||||
| chr7:45684235
|
T | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(171): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1984-744T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684235 | ||||||
| chr7:45684305
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1984-674C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684305 | ||||||
| chr7:45684351
|
C | T | 80 | a0001c0001t0002g0016a0001c0001t0002g0036a0001c0001t0002g0062others(77): Show | 81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1984-628C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684351 | ||||||
| chr7:45684608
|
CAAA | C | 5 | a0001c0001t0009g0080a0001c0001t0009g0083a0001c0001t0009g0084others(2): Show | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1984-370_1984-368d others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684608 | ||||||
| chr7:45684691
|
C | T | 3 | a0001c0001t0002g0089a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG00280.hp2 HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1984-288C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 11/19 | chr7 | 45684691 | ||||||
| chr7:45685097
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0068others(44): Show | 47 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2073+29T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685097 | ||||||
| chr7:45685182
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2073+114A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685182 | ||||||
| chr7:45685260
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2073+192G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685260 | ||||||
| chr7:45685423
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(180): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2073+355G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685423 | ||||||
| chr7:45685528
|
C | G | 1 | a0001c0001t0035g0058 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2074-434C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685528 | ||||||
| chr7:45685534
|
G | A | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2074-428G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685534 | ||||||
| chr7:45685575
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2074-387C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685575 | ||||||
| chr7:45685841
|
C | T | 2 | a0001c0001t0005g0182a0001c0007t0005g0233 | 2 | HG01358.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2074-121C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685841 | ||||||
| chr7:45685886
|
G | T | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2074-76G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 12/19 | chr7 | 45685886 | ||||||
| chr7:45686246
|
T | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0036 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2327+31T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686246 | ||||||
| chr7:45686253
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2327+38C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686253 | ||||||
| chr7:45686394
|
A | G | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2328-153A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686394 | ||||||
| chr7:45686395
|
T | C | 1 | a0001c0001t0010g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2328-152T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686395 | ||||||
| chr7:45686402
|
T | A | 11 | a0001c0002t0003g0121a0001c0002t0003g0196a0001c0002t0003g0247others(8): Show | 11 | HG00609.hp2 HG02083.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.2328-145T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686402 | ||||||
| chr7:45686407
|
C | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2328-140C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686407 | ||||||
| chr7:45686427
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2328-120G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 13/19 | chr7 | 45686427 | ||||||
| chr7:45686853
|
G | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(178): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2454+180G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45686853 | ||||||
| chr7:45686866
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0169 | 3 | NA18952.hp1 NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2454+193G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45686866 | ||||||
| chr7:45686904
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(177): Show | 183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2454+231G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45686904 | ||||||
| chr7:45686906
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2454+233G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45686906 | ||||||
| chr7:45686978
|
C | T | 1 | a0001c0002t0003g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2454+305C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45686978 | ||||||
| chr7:45687067
|
G | A | 2 | a0001c0001t0005g0158a0001c0001t0005g0220 | 2 | NA18960.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2454+394G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687067 | ||||||
| chr7:45687172
|
G | A | 1 | a0007c0017t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2454+499G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687172 | ||||||
| chr7:45687207
|
AG | A | 69 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(66): Show | 69 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.2454+535delG | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687207 | ||||||
| chr7:45687461
|
C | T | 1 | a0001c0002t0003g0126 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2454+788C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687461 | ||||||
| chr7:45687475
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(183): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2454+802A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687475 | ||||||
| chr7:45687647
|
A | T | 1 | a0004c0011t0001g0178 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2454+974A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687647 | ||||||
| chr7:45687808
|
G | C | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2454+1135G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687808 | ||||||
| chr7:45687997
|
A | C | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2454+1324A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45687997 | ||||||
| chr7:45688057
|
G | C | 24 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(21): Show | 24 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+1384G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688057 | ||||||
| chr7:45688063
|
G | T | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+1390G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688063 | ||||||
| chr7:45688072
|
G | A | 1 | a0001c0002t0026g0005 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2454+1399G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688072 | ||||||
| chr7:45688088
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2454+1415G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688088 | ||||||
| chr7:45688093
|
G | T | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(3): Show | 6 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+1420G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688093 | ||||||
| chr7:45688184
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+1511C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688184 | ||||||
| chr7:45688269
|
T | C | 1 | a0001c0001t0054g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2454+1596T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688269 | ||||||
| chr7:45688270
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2454+1597C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688270 | ||||||
| chr7:45688347
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(183): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2454+1674A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688347 | ||||||
| chr7:45688436
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2454+1763G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688436 | ||||||
| chr7:45688472
|
G | A | 3 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0077g0012 | 3 | HG00140.hp2 HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2454+1799G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688472 | ||||||
| chr7:45688539
|
G | A | 1 | a0005c0010t0013g0246 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2454+1866G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688539 | ||||||
| chr7:45688675
|
T | C | 1 | a0001c0002t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2454+2002T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688675 | ||||||
| chr7:45688754
|
T | C | 1 | a0001c0002t0003g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2454+2081T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688754 | ||||||
| chr7:45688800
|
G | T | 4 | a0001c0001t0002g0216a0001c0001t0002g0221a0001c0001t0073g0207others(1): Show | 4 | NA18960.hp2 NA19010.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+2127G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45688800 | ||||||
| chr7:45689313
|
A | G | 2 | a0001c0002t0003g0115a0001c0002t0003g0126 | 2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2454+2640A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689313 | ||||||
| chr7:45689434
|
T | C | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2454+2761T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689434 | ||||||
| chr7:45689481
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(101): Show | 107 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2454+2808G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689481 | ||||||
| chr7:45689516
|
C | T | 2 | a0001c0002t0003g0006a0001c0002t0003g0195 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2454+2843C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689516 | ||||||
| chr7:45689558
|
G | A | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454+2885G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689558 | ||||||
| chr7:45689559
|
C | T | 5 | a0001c0001t0002g0097a0001c0001t0002g0135a0001c0001t0002g0155others(2): Show | 5 | HG02109.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454+2886C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689559 | ||||||
| chr7:45689768
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0169 | 3 | NA18952.hp1 NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2454+3095C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689768 | ||||||
| chr7:45689784
|
G | T | 1 | a0001c0005t0025g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2454+3111G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689784 | ||||||
| chr7:45689928
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0156others(12): Show | 15 | HG01261.hp1 HG01928.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454+3255A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45689928 | ||||||
| chr7:45690164
|
A | T | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+3491A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690164 | ||||||
| chr7:45690446
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0068g0180 | 2 | HG02258.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2454+3773C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690446 | ||||||
| chr7:45690447
|
G | A | 2 | a0001c0001t0004g0163a0001c0018t0004g0154 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2454+3774G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690447 | ||||||
| chr7:45690519
|
C | T | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2454+3846C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690519 | ||||||
| chr7:45690592
|
C | T | 1 | a0001c0001t0051g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2454+3919C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690592 | ||||||
| chr7:45690598
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(187): Show | 193 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2454+3925T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690598 | ||||||
| chr7:45690695
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0238a0001c0001t0052g0256 | 4 | HG02683.hp2 NA18954.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+4022T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45690695 | ||||||
| chr7:45691115
|
T | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(249): Show | 255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2454+4442T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691115 | ||||||
| chr7:45691188
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2454+4515C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691188 | ||||||
| chr7:45691203
|
A | G | 3 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0077g0012 | 3 | HG00140.hp2 HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2454+4530A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691203 | ||||||
| chr7:45691232
|
A | G | 1 | a0001c0002t0026g0005 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2454+4559A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691232 | ||||||
| chr7:45691255
|
G | A | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2454+4582G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691255 | ||||||
| chr7:45691377
|
C | G | 4 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+4704C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691377 | ||||||
| chr7:45691449
|
G | A | 6 | a0001c0001t0002g0159a0001c0001t0002g0162a0001c0001t0002g0170others(3): Show | 6 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+4776G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691449 | ||||||
| chr7:45691545
|
C | T | 11 | a0001c0001t0068g0180a0001c0002t0003g0015a0001c0002t0003g0017others(8): Show | 11 | HG01106.hp1 HG02071.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2454+4872C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691545 | ||||||
| chr7:45691572
|
T | A | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2454+4899T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691572 | ||||||
| chr7:45691720
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2454+5047C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691720 | ||||||
| chr7:45691750
|
A | C | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2454+5077A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691750 | ||||||
| chr7:45691803
|
T | G | 1 | a0001c0001t0043g0146 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2454+5130T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691803 | ||||||
| chr7:45691933
|
ATATAAAG others(18): Show |
A | 1 | a0001c0001t0017g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2454+5262_2454+528 others(29): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45691933 | |||||
| chr7:45691979
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2454+5306C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691979 | ||||||
| chr7:45691984
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2454+5311G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45691984 | ||||||
| chr7:45692001
|
C | T | 96 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.2454+5328C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692001 | ||||||
| chr7:45692134
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2454+5461G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692134 | ||||||
| chr7:45692219
|
A | C | 1 | a0001c0002t0011g0167 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2454+5546A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692219 | ||||||
| chr7:45692249
|
C | T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+5576C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692249 | ||||||
| chr7:45692476
|
G | A | 90 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2454+5803G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692476 | ||||||
| chr7:45692587
|
C | T | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2454+5914C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692587 | ||||||
| chr7:45692626
|
T | C | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2454+5953T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692626 | ||||||
| chr7:45692753
|
C | T | 6 | a0001c0001t0002g0087a0001c0001t0020g0039a0001c0001t0020g0042others(3): Show | 6 | HG00408.hp1 HG00408.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+6080C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692753 | ||||||
| chr7:45692773
|
T | C | 4 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+6100T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692773 | ||||||
| chr7:45692846
|
T | TA | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+6182dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45692846 | |||||
| chr7:45692984
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2454+6311A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45692984 | ||||||
| chr7:45693013
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2454+6340A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693013 | ||||||
| chr7:45693091
|
C | T | 87 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(84): Show | 88 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2454+6418C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693091 | ||||||
| chr7:45693095
|
C | G | 1 | a0001c0001t0058g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2454+6422C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693095 | ||||||
| chr7:45693144
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(174): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2454+6471C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693144 | ||||||
| chr7:45693158
|
C | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(180): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2454+6485C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693158 | ||||||
| chr7:45693181
|
A | G | 2 | a0001c0002t0026g0005a0001c0002t0026g0264 | 2 | HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2454+6508A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693181 | ||||||
| chr7:45693186
|
A | G | 24 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(21): Show | 24 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+6513A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693186 | ||||||
| chr7:45693244
|
T | G | 43 | a0001c0001t0066g0024a0001c0002t0003g0006a0001c0002t0003g0015others(40): Show | 43 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2454+6571T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693244 | ||||||
| chr7:45693289
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2454+6616A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693289 | ||||||
| chr7:45693292
|
T | A | 2 | a0001c0002t0026g0005a0001c0002t0026g0264 | 2 | HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2454+6619T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693292 | ||||||
| chr7:45693370
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2454+6697C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693370 | ||||||
| chr7:45693394
|
C | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(269): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2454+6721C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693394 | ||||||
| chr7:45693539
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(175): Show | 181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2454+6866A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693539 | ||||||
| chr7:45693731
|
A | G | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+7058A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693731 | ||||||
| chr7:45693811
|
T | C | 2 | a0001c0001t0056g0241a0007c0017t0001g0153 | 2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2454+7138T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693811 | ||||||
| chr7:45693830
|
T | C | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2454+7157T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693830 | ||||||
| chr7:45693929
|
C | T | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2454+7256C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693929 | ||||||
| chr7:45693940
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2454+7267G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693940 | ||||||
| chr7:45693944
|
A | G | 4 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+7271A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693944 | ||||||
| chr7:45693978
|
G | C | 1 | a0001c0001t0030g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2454+7305G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45693978 | ||||||
| chr7:45694002
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(269): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2454+7329C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694002 | ||||||
| chr7:45694038
|
C | T | 8 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(5): Show | 8 | HG00140.hp2 HG00673.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454+7365C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694038 | ||||||
| chr7:45694039
|
G | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2454+7366G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694039 | ||||||
| chr7:45694058
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(174): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2454+7385A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694058 | ||||||
| chr7:45694074
|
G | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(178): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2454+7401G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694074 | ||||||
| chr7:45694075
|
C | T | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2454+7402C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694075 | ||||||
| chr7:45694112
|
T | TA | 3 | a0001c0002t0003g0021a0001c0002t0003g0131a0001c0002t0003g0251 | 3 | HG01071.hp2 HG02083.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2454+7441dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694112 | |||||
| chr7:45694114
|
AT | A | 3 | a0001c0002t0011g0014a0001c0002t0011g0167a0001c0002t0026g0264 | 3 | HG01433.hp2 HG02071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2454+7442delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694114 | ||||||
| chr7:45694115
|
T | A | 41 | a0001c0001t0066g0024a0001c0002t0003g0006a0001c0002t0003g0015others(38): Show | 41 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2454+7442T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694115 | ||||||
| chr7:45694115
|
T | TA | 25 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(22): Show | 25 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.2454+7464dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694115 | |||||
| chr7:45694115
|
TA | T | 11 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(8): Show | 11 | HG00140.hp2 HG00673.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2454+7464delA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694115 | |||||
| chr7:45694115
|
TAAA | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0208a0001c0001t0001g0229others(3): Show | 6 | NA18955.hp2 NA18994.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.2454+7462_2454+746 others(7): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694115 | |||||
| chr7:45694115
|
TAAAA | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(141): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2454+7461_2454+746 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694115 | |||||
| chr7:45694115
|
TAAAAA | T | 25 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(22): Show | 26 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.2454+7460_2454+746 others(9): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45694115 | |||||
| chr7:45694145
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0077 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2454+7472A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694145 | ||||||
| chr7:45694479
|
A | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2454+7806A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694479 | ||||||
| chr7:45694604
|
T | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+7931T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694604 | ||||||
| chr7:45694721
|
G | A | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+8048G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694721 | ||||||
| chr7:45694897
|
C | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(86): Show | 91 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2454+8224C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694897 | ||||||
| chr7:45694897
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2454+8224C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694897 | ||||||
| chr7:45694924
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+8251A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694924 | ||||||
| chr7:45694974
|
G | A | 2 | a0001c0001t0004g0198a0001c0001t0004g0199 | 2 | NA18975.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2454+8301G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45694974 | ||||||
| chr7:45695043
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(180): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2455-8333T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695043 | ||||||
| chr7:45695059
|
C | A | 2 | a0001c0002t0003g0119a0001c0002t0003g0120 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2455-8317C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695059 | ||||||
| chr7:45695103
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(180): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2455-8273T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695103 | ||||||
| chr7:45695664
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2455-7712A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695664 | ||||||
| chr7:45695673
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2455-7703A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695673 | ||||||
| chr7:45695883
|
A | G | 1 | a0001c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2455-7493A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45695883 | ||||||
| chr7:45696004
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2455-7372T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696004 | ||||||
| chr7:45696087
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(176): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.2455-7289T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696087 | ||||||
| chr7:45696150
|
G | GGC | 3 | a0001c0002t0003g0115a0001c0002t0003g0126a0001c0002t0064g0094 | 3 | HG01257.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2455-7226_2455-722 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696150 | ||||||
| chr7:45696154
|
T | G | 3 | a0001c0002t0003g0115a0001c0002t0003g0126a0001c0002t0064g0094 | 3 | HG01257.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2455-7222T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696154 | ||||||
| chr7:45696155
|
T | TTAAGAAA others(44): Show |
3 | a0001c0002t0003g0115a0001c0002t0003g0126a0001c0002t0064g0094 | 3 | HG01257.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2455-7221_2455-722 others(55): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696155 | ||||||
| chr7:45696156
|
C | T | 3 | a0001c0002t0003g0115a0001c0002t0003g0126a0001c0002t0064g0094 | 3 | HG01257.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2455-7220C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696156 | ||||||
| chr7:45696164
|
C | T | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2455-7212C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696164 | ||||||
| chr7:45696167
|
C | G | 3 | a0001c0002t0003g0115a0001c0002t0003g0126a0001c0002t0064g0094 | 3 | HG01257.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2455-7209C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696167 | ||||||
| chr7:45696176
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(252): Show | 258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2455-7200T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696176 | ||||||
| chr7:45696265
|
C | T | 25 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0152others(22): Show | 26 | HG00280.hp1 HG00438.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2455-7111C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696265 | ||||||
| chr7:45696438
|
CA | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(189): Show | 195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2455-6916delA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45696438 | |||||
| chr7:45696438
|
CAA | C | 46 | a0001c0001t0002g0036a0001c0001t0002g0076a0001c0001t0002g0187others(43): Show | 46 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.2455-6917_2455-691 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45696438 | |||||
| chr7:45696641
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2455-6735C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696641 | ||||||
| chr7:45696671
|
G | A | 1 | a0001c0001t0005g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2455-6705G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696671 | ||||||
| chr7:45696814
|
G | T | 3 | a0001c0001t0002g0109a0001c0001t0002g0148a0001c0001t0002g0262 | 3 | HG00609.hp1 NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2455-6562G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696814 | ||||||
| chr7:45696815
|
G | C | 3 | a0001c0001t0002g0109a0001c0001t0002g0148a0001c0001t0002g0262 | 3 | HG00609.hp1 NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2455-6561G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696815 | ||||||
| chr7:45696816
|
A | C | 3 | a0001c0001t0002g0109a0001c0001t0002g0148a0001c0001t0002g0262 | 3 | HG00609.hp1 NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2455-6560A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696816 | ||||||
| chr7:45696879
|
G | A | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2455-6497G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45696879 | ||||||
| chr7:45697241
|
T | C | 4 | a0001c0002t0011g0014a0001c0002t0011g0112a0001c0002t0011g0142others(1): Show | 4 | HG01433.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-6135T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697241 | ||||||
| chr7:45697286
|
G | A | 1 | a0001c0002t0011g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2455-6090G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697286 | ||||||
| chr7:45697303
|
A | T | 1 | a0001c0001t0002g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2455-6073A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697303 | ||||||
| chr7:45697386
|
C | CT | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(165): Show | 171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2455-5969dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45697386 | |||||
| chr7:45697386
|
C | CTT | 7 | a0001c0001t0001g0215a0001c0001t0002g0135a0001c0001t0005g0231others(4): Show | 7 | HG01261.hp1 HG02027.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2455-5970_2455-596 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45697386 | |||||
| chr7:45697386
|
CT | C | 6 | a0001c0001t0008g0009a0001c0001t0034g0047a0001c0002t0003g0006others(3): Show | 6 | HG03041.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-5969delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45697386 | |||||
| chr7:45697486
|
G | C | 3 | a0002c0003t0007g0031a0002c0003t0007g0032a0002c0003t0007g0033 | 3 | HG01257.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2455-5890G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697486 | ||||||
| chr7:45697665
|
C | T | 1 | a0001c0008t0001g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2455-5711C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697665 | ||||||
| chr7:45697878
|
T | A | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(178): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2455-5498T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697878 | ||||||
| chr7:45697892
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2455-5484C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697892 | ||||||
| chr7:45697952
|
A | G | 2 | a0001c0002t0003g0117a0001c0002t0003g0181 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2455-5424A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697952 | ||||||
| chr7:45697978
|
A | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0169others(2): Show | 5 | NA18942.hp1 NA18952.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2455-5398A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45697978 | ||||||
| chr7:45698067
|
T | C | 1 | a0001c0001t0005g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2455-5309T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698067 | ||||||
| chr7:45698164
|
T | TAC | 4 | a0001c0001t0002g0016a0001c0001t0002g0036a0001c0001t0002g0221others(1): Show | 4 | HG02451.hp1 HG03471.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-5188_2455-518 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45698164 | |||||
| chr7:45698164
|
T | TACAC | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2455-5190_2455-518 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45698164 | |||||
| chr7:45698164
|
TACAC | T | 4 | a0001c0001t0005g0185a0001c0001t0048g0064a0001c0001t0070g0065others(1): Show | 4 | HG01884.hp1 HG03041.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-5190_2455-518 others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 45698164 | |||||
| chr7:45698184
|
C | A | 1 | a0001c0005t0025g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2455-5192C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698184 | ||||||
| chr7:45698190
|
T | C | 1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2455-5186T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698190 | ||||||
| chr7:45698202
|
G | C | 44 | a0001c0001t0068g0180a0001c0002t0003g0006a0001c0002t0003g0015others(41): Show | 44 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2455-5174G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698202 | ||||||
| chr7:45698239
|
T | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2455-5137T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698239 | ||||||
| chr7:45698586
|
C | T | 1 | a0001c0002t0050g0260 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2455-4790C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698586 | ||||||
| chr7:45698640
|
C | T | 1 | a0001c0002t0011g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2455-4736C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45698640 | ||||||
| chr7:45699030
|
A | C | 4 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-4346A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699030 | ||||||
| chr7:45699347
|
T | G | 1 | a0001c0001t0052g0256 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2455-4029T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699347 | ||||||
| chr7:45699362
|
G | C | 1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2455-4014G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699362 | ||||||
| chr7:45699392
|
C | T | 1 | a0001c0001t0053g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2455-3984C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699392 | ||||||
| chr7:45699421
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2455-3955G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699421 | ||||||
| chr7:45699553
|
G | A | 1 | a0001c0002t0075g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2455-3823G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699553 | ||||||
| chr7:45699559
|
G | C | 2 | a0001c0001t0032g0040a0001c0001t0033g0043 | 2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2455-3817G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699559 | ||||||
| chr7:45699593
|
G | A | 3 | a0001c0001t0017g0141a0001c0001t0017g0193a0001c0007t0017g0234 | 3 | HG00280.hp1 HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2455-3783G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699593 | ||||||
| chr7:45699759
|
G | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(87): Show | 92 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2455-3617G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699759 | ||||||
| chr7:45699776
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(174): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2455-3600T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699776 | ||||||
| chr7:45699974
|
C | A | 1 | a0001c0002t0050g0260 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2455-3402C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45699974 | ||||||
| chr7:45700098
|
A | T | 1 | a0001c0001t0057g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2455-3278A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700098 | ||||||
| chr7:45700103
|
G | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2455-3273G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700103 | ||||||
| chr7:45700274
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2455-3102C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700274 | ||||||
| chr7:45700529
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2455-2847G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700529 | ||||||
| chr7:45700549
|
C | A | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2455-2827C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700549 | ||||||
| chr7:45700584
|
G | A | 2 | a0001c0002t0026g0005a0001c0002t0026g0264 | 2 | HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2455-2792G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700584 | ||||||
| chr7:45700717
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(267): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2455-2659T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700717 | ||||||
| chr7:45700717
|
T | G | 1 | a0001c0001t0002g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2455-2659T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700717 | ||||||
| chr7:45700969
|
C | T | 6 | a0001c0001t0002g0159a0001c0001t0002g0162a0001c0001t0002g0170others(3): Show | 6 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-2407C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700969 | ||||||
| chr7:45700976
|
A | G | 4 | a0001c0002t0011g0014a0001c0002t0011g0112a0001c0002t0011g0142others(1): Show | 4 | HG01433.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-2400A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45700976 | ||||||
| chr7:45701022
|
T | A | 15 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(12): Show | 16 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.2455-2354T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701022 | ||||||
| chr7:45701293
|
C | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0030others(47): Show | 50 | HG00438.hp1 HG00738.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.2455-2083C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701293 | ||||||
| chr7:45701399
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2455-1977T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701399 | ||||||
| chr7:45701429
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2455-1947A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701429 | ||||||
| chr7:45701445
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2455-1931G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701445 | ||||||
| chr7:45701472
|
G | A | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2455-1904G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701472 | ||||||
| chr7:45701490
|
C | T | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-1886C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701490 | ||||||
| chr7:45701586
|
T | G | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2455-1790T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701586 | ||||||
| chr7:45701649
|
A | G | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2455-1727A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701649 | ||||||
| chr7:45701687
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2455-1689C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701687 | ||||||
| chr7:45701694
|
C | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(271): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2455-1682C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701694 | ||||||
| chr7:45701817
|
G | C | 1 | a0001c0001t0002g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2455-1559G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701817 | ||||||
| chr7:45701834
|
C | T | 1 | a0001c0001t0012g0202 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2455-1542C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701834 | ||||||
| chr7:45701926
|
C | T | 43 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(40): Show | 43 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2455-1450C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701926 | ||||||
| chr7:45701930
|
C | T | 4 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-1446C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701930 | ||||||
| chr7:45701965
|
A | C | 4 | a0001c0001t0001g0249a0001c0001t0015g0041a0001c0013t0001g0223others(1): Show | 4 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-1411A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701965 | ||||||
| chr7:45701980
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2455-1396A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45701980 | ||||||
| chr7:45702089
|
G | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2455-1287G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702089 | ||||||
| chr7:45702097
|
G | A | 2 | a0001c0001t0068g0180a0004c0011t0001g0178 | 2 | HG02258.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2455-1279G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702097 | ||||||
| chr7:45702164
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(174): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2455-1212C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702164 | ||||||
| chr7:45702207
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2455-1169C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702207 | ||||||
| chr7:45702246
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(249): Show | 255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2455-1130A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702246 | ||||||
| chr7:45702280
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2455-1096T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702280 | ||||||
| chr7:45702344
|
G | A | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2455-1032G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702344 | ||||||
| chr7:45702372
|
C | T | 24 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(21): Show | 24 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2455-1004C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702372 | ||||||
| chr7:45702552
|
G | C | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2455-824G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702552 | ||||||
| chr7:45702566
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2455-810G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702566 | ||||||
| chr7:45702755
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2455-621C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702755 | ||||||
| chr7:45702886
|
C | T | 1 | a0001c0001t0016g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2455-490C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702886 | ||||||
| chr7:45702907
|
G | C | 4 | a0001c0002t0011g0014a0001c0002t0011g0112a0001c0002t0011g0142others(1): Show | 4 | HG01433.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-469G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45702907 | ||||||
| chr7:45703021
|
G | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(87): Show | 92 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2455-355G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45703021 | ||||||
| chr7:45703128
|
G | A | 4 | a0001c0001t0057g0010a0001c0001t0058g0071a0001c0006t0023g0078others(1): Show | 4 | HG02735.hp2 HG03239.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-248G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45703128 | ||||||
| chr7:45703219
|
T | C | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2455-157T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 14/19 | chr7 | 45703219 | ||||||
| chr7:45703529
|
T | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(108): Show | 114 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2571+37T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 15/19 | chr7 | 45703529 | ||||||
| chr7:45703804
|
G | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(269): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2718+58G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45703804 | ||||||
| chr7:45703812
|
A | G | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2718+66A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45703812 | ||||||
| chr7:45703840
|
C | T | 3 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0014t0004g0164 | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2718+94C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45703840 | ||||||
| chr7:45703939
|
C | G | 48 | a0001c0001t0068g0180a0001c0002t0003g0006a0001c0002t0003g0015others(45): Show | 48 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2718+193C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45703939 | ||||||
| chr7:45704222
|
C | G | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2719-296C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704222 | ||||||
| chr7:45704228
|
C | A | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2719-290C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704228 | ||||||
| chr7:45704268
|
G | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(108): Show | 114 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2719-250G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704268 | ||||||
| chr7:45704373
|
T | A | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2719-145T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704373 | ||||||
| chr7:45704426
|
A | G | 1 | a0001c0001t0002g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2719-92A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704426 | ||||||
| chr7:45704456
|
C | T | 54 | a0001c0001t0068g0180a0001c0002t0003g0006a0001c0002t0003g0015others(51): Show | 54 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2719-62C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704456 | ||||||
| chr7:45704465
|
C | T | 2 | a0001c0001t0028g0133a0001c0001t0028g0211 | 2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2719-53C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 16/19 | chr7 | 45704465 | ||||||
| chr7:45704632
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2817+16C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45704632 | ||||||
| chr7:45704755
|
T | C | 1 | a0001c0001t0070g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2817+139T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45704755 | ||||||
| chr7:45704822
|
T | G | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2817+206T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45704822 | ||||||
| chr7:45704833
|
C | T | 44 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(41): Show | 44 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2817+217C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45704833 | ||||||
| chr7:45705056
|
A | G | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2817+440A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705056 | ||||||
| chr7:45705065
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(93): Show | 98 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2817+449G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705065 | ||||||
| chr7:45705161
|
C | G | 1 | a0001c0001t0046g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2817+545C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705161 | ||||||
| chr7:45705333
|
G | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2817+717G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705333 | ||||||
| chr7:45705380
|
C | G | 7 | a0001c0001t0068g0180a0001c0002t0014g0099a0001c0002t0014g0101others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817+764C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705380 | ||||||
| chr7:45705503
|
T | C | 68 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(65): Show | 68 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.2817+887T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705503 | ||||||
| chr7:45705642
|
C | T | 1 | a0001c0001t0005g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2817+1026C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705642 | ||||||
| chr7:45705673
|
C | T | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2817+1057C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705673 | ||||||
| chr7:45705820
|
A | G | 3 | a0001c0002t0003g0268a0001c0002t0003g0269a0001c0002t0003g0270 | 3 | NA18948.hp1 NA19011.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2817+1204A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45705820 | ||||||
| chr7:45706492
|
C | CA | 130 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0036others(127): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2818-1837dupA | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr7 | 45706492 | |||||
| chr7:45706492
|
C | CAA | 22 | a0001c0001t0002g0217a0001c0001t0004g0066a0001c0001t0004g0096others(19): Show | 22 | HG01109.hp2 HG01168.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.2818-1838_2818-183 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr7 | 45706492 | |||||
| chr7:45706492
|
C | CAAA | 8 | a0001c0001t0004g0067a0001c0001t0004g0198a0001c0001t0006g0044others(5): Show | 8 | HG00423.hp2 HG04228.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-1839_2818-183 others(7): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr7 | 45706492 | |||||
| chr7:45706492
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0019g0038a0001c0002t0049g0007 | 2 | HG02074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2818-1846_2818-183 others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr7 | 45706492 | |||||
| chr7:45706512
|
A | AG | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(78): Show | 83 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2818-1838_2818-183 others(5): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706512 | ||||||
| chr7:45706512
|
A | G | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0114others(3): Show | 6 | HG00738.hp1 HG02027.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-1838A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706512 | ||||||
| chr7:45706563
|
A | G | 41 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(38): Show | 41 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2818-1787A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706563 | ||||||
| chr7:45706646
|
G | A | 3 | a0001c0001t0016g0028a0001c0001t0016g0098a0001c0001t0016g0235 | 3 | HG03098.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2818-1704G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706646 | ||||||
| chr7:45706789
|
A | T | 2 | a0001c0001t0004g0163a0001c0018t0004g0154 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2818-1561A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706789 | ||||||
| chr7:45706817
|
G | A | 7 | a0001c0002t0003g0015a0001c0002t0003g0017a0001c0002t0003g0018others(4): Show | 7 | HG02257.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2818-1533G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706817 | ||||||
| chr7:45706982
|
T | C | 1 | a0001c0002t0003g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2818-1368T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45706982 | ||||||
| chr7:45707077
|
G | A | 47 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(44): Show | 47 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2818-1273G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45707077 | ||||||
| chr7:45707480
|
C | T | 6 | a0001c0001t0012g0201a0001c0001t0012g0202a0001c0001t0012g0213others(3): Show | 6 | HG02071.hp2 NA18978.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-870C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45707480 | ||||||
| chr7:45708084
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2818-266C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45708084 | ||||||
| chr7:45708334
|
A | G | 42 | a0001c0001t0066g0024a0001c0002t0003g0006a0001c0002t0003g0015others(39): Show | 42 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.2818-16A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 17/19 | chr7 | 45708334 | ||||||
| chr7:45708531
|
G | A | 1 | a0001c0001t0010g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2932+67G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708531 | ||||||
| chr7:45708723
|
C | T | 1 | a0001c0001t0004g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2932+259C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708723 | ||||||
| chr7:45708782
|
G | A | 2 | a0001c0001t0001g0114a0001c0012t0045g0035 | 2 | HG00738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2932+318G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708782 | ||||||
| chr7:45708790
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2932+326C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708790 | ||||||
| chr7:45708825
|
A | G | 2 | a0001c0005t0025g0122a0001c0005t0025g0173 | 2 | HG01106.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2932+361A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708825 | ||||||
| chr7:45708837
|
C | T | 1 | a0001c0001t0042g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2932+373C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708837 | ||||||
| chr7:45708921
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(88): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2932+457T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708921 | ||||||
| chr7:45708968
|
GT | G | 50 | a0001c0001t0001g0257a0001c0001t0002g0097a0001c0001t0002g0135others(47): Show | 50 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.2932+515delT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr7 | 45708968 | |||||
| chr7:45708969
|
T | G | 2 | a0001c0001t0001g0023a0001c0001t0039g0150 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2932+505T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45708969 | ||||||
| chr7:45709036
|
T | C | 2 | a0001c0001t0020g0039a0001c0001t0020g0042 | 2 | NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2932+572T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709036 | ||||||
| chr7:45709095
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2932+631A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709095 | ||||||
| chr7:45709255
|
C | G | 2 | a0001c0002t0026g0005a0001c0002t0026g0264 | 2 | HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2932+791C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709255 | ||||||
| chr7:45709304
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2932+840C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709304 | ||||||
| chr7:45709332
|
T | A | 1 | a0001c0001t0002g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2932+868T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709332 | ||||||
| chr7:45709391
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2932+927T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709391 | ||||||
| chr7:45709791
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2933-737C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709791 | ||||||
| chr7:45709809
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0215a0001c0001t0001g0238others(1): Show | 5 | HG02683.hp2 NA18941.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-719C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709809 | ||||||
| chr7:45709866
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2933-662C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709866 | ||||||
| chr7:45709921
|
G | T | 1 | a0001c0001t0068g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2933-607G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709921 | ||||||
| chr7:45709927
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2933-601G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709927 | ||||||
| chr7:45709935
|
A | G | 98 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(95): Show | 99 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.2933-593A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45709935 | ||||||
| chr7:45710035
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2933-493C>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710035 | ||||||
| chr7:45710050
|
A | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(188): Show | 194 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.2933-478A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710050 | ||||||
| chr7:45710077
|
A | G | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2933-451A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710077 | ||||||
| chr7:45710088
|
C | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(88): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2933-440C>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710088 | ||||||
| chr7:45710102
|
G | A | 3 | a0001c0001t0043g0146a0001c0001t0044g0118a0001c0012t0045g0035 | 3 | HG00738.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2933-426G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710102 | ||||||
| chr7:45710174
|
C | T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2933-354C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710174 | ||||||
| chr7:45710494
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2933-34G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 18/19 | chr7 | 45710494 | ||||||
| chr7:45710969
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(90): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.3057+317G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45710969 | ||||||
| chr7:45711289
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3057+637G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711289 | ||||||
| chr7:45711474
|
T | C | 2 | a0001c0001t0043g0146a0001c0012t0045g0035 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3057+822T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711474 | ||||||
| chr7:45711607
|
G | GTA | 4 | a0001c0001t0005g0220a0001c0001t0005g0230a0001c0001t0005g0231others(1): Show | 4 | HG04228.hp2 NA19066.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3057+992_3057+993d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATA | 4 | a0001c0001t0005g0182a0001c0001t0005g0185a0001c0001t0044g0118others(1): Show | 4 | HG00738.hp2 HG01358.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.3057+990_3057+993d others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATATA | 8 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0194others(5): Show | 9 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.3057+988_3057+993d others(8): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0008g0008a0001c0001t0008g0011a0001c0001t0008g0013others(1): Show | 4 | HG00140.hp2 HG00673.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3057+986_3057+993d others(10): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATATAT others(3): Show |
5 | a0001c0001t0006g0051a0001c0001t0008g0009a0001c0001t0009g0086others(2): Show | 5 | HG02970.hp2 HG03516.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.3057+984_3057+993d others(12): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATATAT others(7): Show |
1 | a0001c0012t0045g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3057+980_3057+993d others(16): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0069g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3057+978_3057+993d others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
GTA | G | 20 | a0001c0001t0002g0075a0001c0001t0002g0089a0001c0001t0002g0097others(17): Show | 20 | HG00280.hp2 HG00642.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.3057+992_3057+993d others(4): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
GTATA | G | 44 | a0001c0001t0002g0022a0001c0001t0002g0036a0001c0001t0002g0062others(41): Show | 44 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.3057+990_3057+993d others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
GTATATAT others(9): Show |
G | 6 | a0001c0002t0014g0099a0001c0002t0014g0101a0001c0002t0014g0102others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3057+978_3057+993d others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711607
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3057+972_3057+993d others(24): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711607 | |||||
| chr7:45711611
|
A | C | 1 | a0001c0001t0060g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3057+959A>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711611 | ||||||
| chr7:45711622
|
TATATATA others(23): Show |
T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(91): Show | 96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.3057+972_3057+1001 others(33): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711622 | |||||
| chr7:45711624
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+972T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711624 | ||||||
| chr7:45711624
|
TATATATA others(21): Show |
T | 2 | a0001c0006t0023g0078a0001c0006t0023g0079 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3057+974_3057+1001 others(31): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711624 | |||||
| chr7:45711626
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+974T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711626 | ||||||
| chr7:45711627
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+975A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711627 | ||||||
| chr7:45711630
|
TATATATA others(9): Show |
T | 41 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(38): Show | 41 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.3057+980_3057+995d others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711630 | |||||
| chr7:45711631
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+979A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711631 | ||||||
| chr7:45711632
|
TATATATA others(7): Show |
T | 3 | a0001c0002t0011g0167a0001c0002t0026g0005a0001c0002t0041g0082 | 3 | HG01106.hp1 HG01433.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3057+982_3057+995d others(16): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711632 | |||||
| chr7:45711634
|
TATATATA others(5): Show |
T | 1 | a0001c0002t0026g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3057+984_3057+995d others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711634 | |||||
| chr7:45711636
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+984T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711636 | ||||||
| chr7:45711638
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+986T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711638 | ||||||
| chr7:45711642
|
T | C | 12 | a0001c0001t0002g0089a0001c0001t0002g0218a0001c0001t0002g0221others(9): Show | 12 | HG00280.hp2 HG04199.hp1 NA18957.hp2 others(9): Show |
intron_variant | MODIFIER | c.3057+990T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711642 | ||||||
| chr7:45711644
|
T | C | 64 | a0001c0001t0001g0107a0001c0001t0002g0022a0001c0001t0002g0036others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.3057+992T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711644 | ||||||
| chr7:45711644
|
T | TATATACA others(1): Show |
3 | a0001c0001t0004g0199a0001c0001t0006g0049a0001c0001t0034g0047 | 3 | NA18959.hp2 NA18975.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3057+993_3057+994i others(10): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711644
|
T | TATATATA others(3): Show |
5 | a0001c0001t0004g0066a0001c0001t0004g0198a0001c0001t0006g0044others(2): Show | 5 | HG01981.hp1 HG02809.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.3057+993_3057+994i others(12): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711644
|
T | TATATATA others(5): Show |
1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3057+993_3057+994i others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711644
|
T | TATATATA others(5): Show |
8 | a0001c0001t0004g0067a0001c0001t0004g0096a0001c0001t0006g0059others(5): Show | 8 | HG00423.hp2 HG01168.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3057+993_3057+994i others(14): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711644
|
T | TATATATA others(9): Show |
1 | a0001c0001t0004g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3057+993_3057+994i others(18): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711644
|
T | TATATATA others(11): Show |
2 | a0001c0001t0004g0205a0001c0001t0028g0211 | 2 | HG01952.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3057+993_3057+994i others(20): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711644 | |||||
| chr7:45711646
|
C | T | 17 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(14): Show | 18 | HG00738.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.3057+994C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711646 | ||||||
| chr7:45711648
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+996C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711648 | ||||||
| chr7:45711650
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+998C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711650 | ||||||
| chr7:45711652
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1000C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711652 | ||||||
| chr7:45711679
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1027A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711679 | ||||||
| chr7:45711684
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1032C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711684 | ||||||
| chr7:45711686
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1034C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711686 | ||||||
| chr7:45711690
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1038C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711690 | ||||||
| chr7:45711695
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1043A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711695 | ||||||
| chr7:45711699
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3057+1047A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711699 | ||||||
| chr7:45711699
|
ATATATAC others(11): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3057+1072_3057+108 others(22): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711699 | |||||
| chr7:45711731
|
G | A | 27 | a0001c0002t0003g0110a0001c0002t0003g0115a0001c0002t0003g0116others(24): Show | 27 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3057+1079G>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711731 | ||||||
| chr7:45711764
|
T | C | 7 | a0001c0001t0005g0001a0001c0001t0005g0088a0001c0001t0005g0158others(4): Show | 8 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3057+1112T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711764 | ||||||
| chr7:45711821
|
C | CT | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(179): Show | 185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3057+1173dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711821 | |||||
| chr7:45711867
|
A | ATATATTA others(23): Show |
1 | a0001c0001t0063g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3057+1239_3057+126 others(34): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711867 | |||||
| chr7:45711880
|
A | ATAAATAT others(44): Show |
7 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0011others(4): Show | 7 | HG00140.hp2 HG00673.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.3057+1238_3057+128 others(55): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711880 | |||||
| chr7:45711889
|
T | TTTATATA others(22): Show |
49 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(46): Show | 49 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.3057+1265_3057+129 others(33): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711889 | |||||
| chr7:45711889
|
T | TTTATATA others(52): Show |
1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3057+1268_3057+126 others(63): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711889 | |||||
| chr7:45711889
|
TTTATATA others(22): Show |
T | 1 | a0001c0001t0048g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3057+1265_3057+129 others(33): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711889 | |||||
| chr7:45711897
|
T | TTATATTA others(17): Show |
1 | a0001c0002t0064g0094 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3057+1253_3057+127 others(28): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711897 | |||||
| chr7:45711910
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(88): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.3057+1258A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711910 | ||||||
| chr7:45711913
|
A | AAT | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(179): Show | 185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3057+1266_3057+126 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711913 | |||||
| chr7:45711918
|
A | ATTTATAT others(24): Show |
23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.3057+1268_3057+126 others(35): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711918 | |||||
| chr7:45711940
|
T | G | 3 | a0001c0001t0017g0141a0001c0001t0017g0193a0001c0007t0017g0234 | 3 | HG00280.hp1 HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3057+1288T>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711940 | ||||||
| chr7:45711943
|
A | ATATATTT others(29): Show |
1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3057+1293_3057+129 others(40): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711943 | |||||
| chr7:45711946
|
C | T | 1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3057+1294C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45711946 | ||||||
| chr7:45711970
|
C | CATATATT others(15): Show |
83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(80): Show | 85 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.3057+1322_3057+132 others(26): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711970 | |||||
| chr7:45711971
|
ATAT | A | 10 | a0001c0001t0001g0144a0001c0001t0001g0197a0001c0001t0001g0249others(7): Show | 10 | HG00438.hp2 HG00738.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.3057+1323_3057+132 others(7): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711971 | |||||
| chr7:45711971
|
ATATTATA others(21): Show |
A | 1 | a0003c0004t0001g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3057+1323_3057+135 others(32): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45711971 | |||||
| chr7:45712004
|
TTAAATAT others(18): Show |
T | 2 | a0001c0001t0005g0001a0001c0001t0005g0088 | 3 | HG01099.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3057+1372_3057+139 others(29): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45712004 | |||||
| chr7:45712024
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0059g0157 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3057+1372T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712024 | ||||||
| chr7:45712024
|
TTATAC | T | 51 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(48): Show | 51 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.3057+1375_3057+137 others(9): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45712024 | |||||
| chr7:45712029
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(218): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.3057+1377C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712029 | ||||||
| chr7:45712040
|
T | A | 23 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0096others(20): Show | 23 | HG00423.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.3057+1388T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712040 | ||||||
| chr7:45712049
|
A | T | 4 | a0001c0001t0002g0087a0001c0001t0043g0146a0001c0001t0044g0118others(1): Show | 4 | HG00738.hp2 HG02040.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3057+1397A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712049 | ||||||
| chr7:45712068
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3057+1416T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712068 | ||||||
| chr7:45712074
|
T | A | 4 | a0001c0001t0001g0240a0001c0001t0043g0146a0001c0001t0044g0118others(1): Show | 4 | HG00738.hp2 HG01346.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3057+1422T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712074 | ||||||
| chr7:45712080
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3057+1428T>A | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712080 | ||||||
| chr7:45712232
|
A | AAC | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(94): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.3058-1460_3058-145 others(6): Show |
ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45712232 | |||||
| chr7:45712251
|
C | CT | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(95): Show | 100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.3058-1431dupT | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr7 | 45712251 | |||||
| chr7:45712311
|
A | T | 51 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(48): Show | 51 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.3058-1382A>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712311 | ||||||
| chr7:45712398
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(88): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.3058-1295T>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712398 | ||||||
| chr7:45712548
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0039g0150 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3058-1145G>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712548 | ||||||
| chr7:45712774
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3058-919G>C | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712774 | ||||||
| chr7:45712791
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(94): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.3058-902C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712791 | ||||||
| chr7:45712910
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(94): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.3058-783A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712910 | ||||||
| chr7:45712996
|
A | G | 3 | a0001c0001t0017g0141a0001c0001t0017g0193a0001c0007t0017g0234 | 3 | HG00280.hp1 HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3058-697A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45712996 | ||||||
| chr7:45713321
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(88): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.3058-372A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45713321 | ||||||
| chr7:45713459
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0039g0150 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3058-234C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45713459 | ||||||
| chr7:45713567
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3058-126C>T | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45713567 | ||||||
| chr7:45713640
|
A | G | 41 | a0001c0002t0003g0006a0001c0002t0003g0015a0001c0002t0003g0017others(38): Show | 41 | HG00140.hp1 HG00609.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.3058-53A>G | ADCY1 | ENSG00000164742.16 | transcript | ENST00000297323.12 | protein_coding | 19/19 | chr7 | 45713640 |