| geneid | 59284 |
|---|---|
| ensemblid | ENSG00000105605.8 |
| hgncid | 13626 |
| symbol | CACNG7 |
| name | calcium voltage-gated channel auxiliary subunit gamma 7 |
| refseq_nuc | NM_031896.5 |
| refseq_prot | NP_114102.2 |
| ensembl_nuc | ENST00000391767.6 |
| ensembl_prot | ENSP00000375647.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 53909278 |
| end | 53943950 |
| strand | + |
| ver | v1.2 |
| region | chr19:53909278-53943950 |
| region5000 | chr19:53904278-53948950 |
| regionname0 | CACNG7_chr19_53909278_53943950 |
| regionname5000 | CACNG7_chr19_53904278_53948950 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 275 | 364 | 94 | 70 | 142 | 18 | 40 | 96 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 828 | 363 | 93 | 70 | 142 | 18 | 40 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| c0002 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| 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 | 1926 | 289 | 56 | 57 | 128 | 15 | 33 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0002 | 0/0 | 1927 | 30 | 5 | 10 | 8 | 2 | 5 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0003 | 0/0 | 1926 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0004 | 0/0 | 1926 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0005 | 0/0 | 1927 | 6 | 2 | 1 | 2 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0006 | 0/0 | 1927 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0007 | 0/0 | 1926 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0008 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0009 | 0/0 | 1926 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0010 | 0/0 | 1926 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0011 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0012 | 0/0 | 1928 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0013 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0014 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0015 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0016 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0017 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0018 | 0/0 | 1926 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0019 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0020 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0021 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0022 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0023 | 0/0 | 1926 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0024 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| t0025 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| 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 | 4 | 0 | 1 | 3 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 828 | 363 | 93 | 70 | 142 | 18 | 40 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0002 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2753 | 289 | 56 | 57 | 128 | 15 | 33 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0002 | 0/0 | 2754 | 29 | 4 | 10 | 8 | 2 | 5 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0003 | 0/0 | 2753 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0004 | 0/0 | 2753 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0005 | 0/0 | 2754 | 6 | 2 | 1 | 2 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0006 | 0/0 | 2754 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0007 | 0/0 | 2753 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0008 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0009 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0010 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0011 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0012 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0013 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0014 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0015 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0016 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0017 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0018 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0019 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0020 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0021 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0022 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0023 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0024 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0001t0025 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| a0001c0002t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | copy fasta | chr19 | 53904278 | 53948950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0011g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0014g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0016g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0018g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0019g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0020g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0021g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0022g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0023g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0024g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0025g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0158 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0342 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0214 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01261 | hp1 | a0001 | c0001 | t0018 | g0274 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0067 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0348 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0349 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02630 | hp2 | a0001 | c0001 | t0017 | g0063 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0058 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0351 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0068 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0208 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0233 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0347 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0099 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0052 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18939 | hp1 | a0001 | c0001 | t0025 | g0097 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18989 | hp1 | a0001 | c0001 | t0022 | g0268 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19010 | hp2 | a0001 | c0001 | t0024 | g0014 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19077 | hp2 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ASW | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | GIH | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0281 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0009 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0031 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53942218
|
C | T | 1 | a0001c0002 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.753C>T | p.Ser251Ser | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1022/2754 | 753/828 | 251/275 | chr19 | 53942218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53909285
|
A | C | 1 | a0001c0001t0025 | 1 | NA18939.hp1 | 5_prime_UTR_variant | MODIFIER | c.-262A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3547 | chr19 | 53909285 | |||||
| chr19:53909318
|
G | A | 2 | a0001c0001t0003a0001c0001t0008 | 9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-229G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3514 | chr19 | 53909318 | |||||
| chr19:53909365
|
G | C | 1 | a0001c0001t0009 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3467 | chr19 | 53909365 | |||||
| chr19:53909395
|
C | G | 1 | a0001c0001t0024 | 1 | NA19010.hp2 | 5_prime_UTR_variant | MODIFIER | c.-152C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3437 | chr19 | 53909395 | |||||
| chr19:53909450
|
G | A | 1 | a0001c0001t0010 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3382 | chr19 | 53909450 | |||||
| chr19:53942340
|
AG | A | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*53delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 53 | INFO_REALIGN_3_PRIME | chr19 | 53942340 | ||||
| chr19:53942366
|
C | T | 1 | a0001c0001t0023 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 73 | chr19 | 53942366 | |||||
| chr19:53942398
|
C | T | 1 | a0001c0001t0004 | 8 | HG02055.hp2 HG02615.hp1 HG03139.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 105 | chr19 | 53942398 | |||||
| chr19:53942460
|
C | A | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02647.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 167 | chr19 | 53942460 | |||||
| chr19:53942519
|
C | T | 1 | a0001c0001t0022 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 226 | chr19 | 53942519 | |||||
| chr19:53942551
|
C | T | 2 | a0001c0001t0008a0001c0001t0021 | 2 | HG02145.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*258C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 258 | chr19 | 53942551 | |||||
| chr19:53942644
|
G | C | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 351 | chr19 | 53942644 | |||||
| chr19:53942645
|
C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 352 | chr19 | 53942645 | |||||
| chr19:53942656
|
A | G | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 363 | chr19 | 53942656 | |||||
| chr19:53942672
|
G | A | 1 | a0001c0001t0015 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 379 | chr19 | 53942672 | |||||
| chr19:53942720
|
T | C | 1 | a0001c0001t0007 | 2 | HG02451.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*427T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 427 | chr19 | 53942720 | |||||
| chr19:53942906
|
C | A | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 613 | chr19 | 53942906 | |||||
| chr19:53943025
|
C | T | 1 | a0001c0001t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 732 | chr19 | 53943025 | |||||
| chr19:53943186
|
T | A | 2 | a0001c0001t0008a0001c0001t0021 | 2 | HG02145.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*893T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 893 | chr19 | 53943186 | |||||
| chr19:53943275
|
T | C | 2 | a0001c0001t0004a0001c0001t0017 | 9 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*982T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 982 | chr19 | 53943275 | |||||
| chr19:53943441
|
G | A | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1148 | chr19 | 53943441 | |||||
| chr19:53943547
|
A | G | 1 | a0001c0001t0012 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1254 | chr19 | 53943547 | |||||
| chr19:53943600
|
T | TG | 2 | a0001c0001t0005a0001c0001t0012 | 7 | HG00621.hp1 HG01099.hp1 HG02027.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1313dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1314 | INFO_REALIGN_3_PRIME | chr19 | 53943600 | ||||
| chr19:53943681
|
A | T | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1388 | chr19 | 53943681 | |||||
| chr19:53943748
|
T | A | 1 | a0001c0001t0018 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1455T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1455 | chr19 | 53943748 | |||||
| chr19:53943808
|
G | A | 2 | a0001c0001t0011a0001c0001t0019 | 2 | HG02109.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1515G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1515 | chr19 | 53943808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53909612
|
A | T | 2 | a0001c0001t0001g0355a0001c0001t0004g0354 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+95A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909612 | ||||||
| chr19:53909695
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-30+178G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909695 | ||||||
| chr19:53909778
|
A | G | 1 | a0001c0001t0002g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-30+261A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909778 | ||||||
| chr19:53909837
|
AGAGCAGG others(4): Show |
A | 1 | a0001c0001t0001g0352 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-30+322_-30+332del others(11): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53909837 | |||||
| chr19:53909851
|
G | A | 1 | a0001c0001t0013g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30+334G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909851 | ||||||
| chr19:53910003
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 94 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-30+486T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910003 | ||||||
| chr19:53910061
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+544C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910061 | ||||||
| chr19:53910075
|
G | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-30+558G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910075 | ||||||
| chr19:53910085
|
T | C | 1 | a0001c0001t0013g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30+568T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910085 | ||||||
| chr19:53910250
|
G | T | 1 | a0001c0001t0006g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-30+733G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910250 | ||||||
| chr19:53910255
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 49 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30+738G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910255 | ||||||
| chr19:53910279
|
C | T | 44 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0050others(41): Show | 45 | HG00741.hp2 HG01109.hp2 HG02055.hp2 others(42): Show |
intron_variant | MODIFIER | c.-30+762C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910279 | ||||||
| chr19:53910324
|
C | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 7 | HG02896.hp1 HG02897.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+807C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910324 | ||||||
| chr19:53910385
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+868G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910385 | ||||||
| chr19:53910386
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+869G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910386 | ||||||
| chr19:53910387
|
A | T | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+870A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910387 | ||||||
| chr19:53910388
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+871G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910388 | ||||||
| chr19:53910389
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+872G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910389 | ||||||
| chr19:53910392
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+875G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910392 | ||||||
| chr19:53910393
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+876G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910393 | ||||||
| chr19:53910394
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+877G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910394 | ||||||
| chr19:53910396
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+879G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910396 | ||||||
| chr19:53910397
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+880T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910397 | ||||||
| chr19:53910398
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+881G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910398 | ||||||
| chr19:53910404
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+887T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910404 | ||||||
| chr19:53910412
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+895G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910412 | ||||||
| chr19:53910413
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+896G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910413 | ||||||
| chr19:53910415
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+898G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910415 | ||||||
| chr19:53910419
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+902T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910419 | ||||||
| chr19:53910423
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+906G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910423 | ||||||
| chr19:53910424
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+907G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910424 | ||||||
| chr19:53910425
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+908T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910425 | ||||||
| chr19:53910427
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+910G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910427 | ||||||
| chr19:53910433
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+916G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910433 | ||||||
| chr19:53910436
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+919T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910436 | ||||||
| chr19:53910437
|
C | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+920C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910437 | ||||||
| chr19:53910439
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+922A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910439 | ||||||
| chr19:53910451
|
C | G | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+934C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910451 | ||||||
| chr19:53910455
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+938T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910455 | ||||||
| chr19:53910459
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+942G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910459 | ||||||
| chr19:53910460
|
C | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+943C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910460 | ||||||
| chr19:53910466
|
T | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+949T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910466 | ||||||
| chr19:53910468
|
C | A | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+951C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910468 | ||||||
| chr19:53910469
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+952A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910469 | ||||||
| chr19:53910471
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+954G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910471 | ||||||
| chr19:53910513
|
TGATTAGT others(8): Show |
T | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-30+999_-30+1013de others(16): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53910513 | |||||
| chr19:53910625
|
T | A | 1 | a0001c0001t0002g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+1108T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910625 | ||||||
| chr19:53910650
|
G | C | 61 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0033others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30+1133G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910650 | ||||||
| chr19:53910689
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(6): Show | 11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30+1172C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910689 | ||||||
| chr19:53910725
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30+1208T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910725 | ||||||
| chr19:53910783
|
G | C | 61 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0033others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30+1266G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910783 | ||||||
| chr19:53910988
|
G | A | 6 | a0001c0001t0001g0059a0001c0001t0004g0054a0001c0001t0004g0056others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910988 | ||||||
| chr19:53911001
|
A | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-30+1484A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911001 | ||||||
| chr19:53911040
|
T | TTGGTGGT others(2): Show |
91 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 94 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-30+1530_-30+1538d others(11): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911040 | |||||
| chr19:53911073
|
A | ATT | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 97 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-30+1566_-30+1567d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911073 | |||||
| chr19:53911073
|
A | ATTT | 14 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0205others(11): Show | 14 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+1565_-30+1567d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911073 | |||||
| chr19:53911093
|
G | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 100 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-30+1576G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911093 | ||||||
| chr19:53911136
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+1619G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911136 | ||||||
| chr19:53911196
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1607T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911196 | ||||||
| chr19:53911211
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1592G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911211 | ||||||
| chr19:53911226
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-1577C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911226 | ||||||
| chr19:53911383
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1420T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911383 | ||||||
| chr19:53911396
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 101 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-29-1407G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911396 | ||||||
| chr19:53911411
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-1392G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911411 | ||||||
| chr19:53911469
|
G | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(77): Show | 84 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-29-1334G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911469 | ||||||
| chr19:53911527
|
A | C | 9 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(6): Show | 11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-1276A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911527 | ||||||
| chr19:53911570
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(77): Show | 84 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-29-1233G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911570 | ||||||
| chr19:53911626
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-1177G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911626 | ||||||
| chr19:53911638
|
C | T | 10 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-1165C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911638 | ||||||
| chr19:53911646
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1157G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911646 | ||||||
| chr19:53911742
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-29-1061C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911742 | ||||||
| chr19:53912018
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(38): Show | 45 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-29-785A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912018 | ||||||
| chr19:53912085
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-29-718G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912085 | ||||||
| chr19:53912147
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(38): Show | 45 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-29-656A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912147 | ||||||
| chr19:53912238
|
G | A | 1 | a0001c0001t0020g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29-565G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912238 | ||||||
| chr19:53912470
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-333C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912470 | ||||||
| chr19:53912491
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-29-312C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912491 | ||||||
| chr19:53912653
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-150G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912653 | ||||||
| chr19:53912731
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-72C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912731 | ||||||
| chr19:53913047
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.196+20T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913047 | ||||||
| chr19:53913102
|
T | A | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196+75T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913102 | ||||||
| chr19:53913434
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+407C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913434 | ||||||
| chr19:53913555
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196+528G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913555 | ||||||
| chr19:53913589
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+562C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913589 | ||||||
| chr19:53913603
|
A | G | 2 | a0001c0001t0001g0355a0001c0001t0004g0354 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196+576A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913603 | ||||||
| chr19:53913658
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+631C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913658 | ||||||
| chr19:53913716
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0355a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.196+689C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913716 | ||||||
| chr19:53913772
|
A | G | 4 | a0001c0001t0001g0188a0001c0001t0001g0343a0001c0001t0001g0344others(1): Show | 4 | HG01106.hp1 HG01123.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-728A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913772 | ||||||
| chr19:53913785
|
T | TA | 54 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 55 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.197-692dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | |||||
| chr19:53913785
|
T | TAA | 43 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(40): Show | 44 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.197-693_197-692dup others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | |||||
| chr19:53913785
|
T | TAAA | 6 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG01106.hp2 HG02300.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-694_197-692dup others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | |||||
| chr19:53913785
|
TA | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(22): Show | 26 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.197-692delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | |||||
| chr19:53913799
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-701A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913799 | ||||||
| chr19:53913802
|
A | AG | 10 | a0001c0001t0001g0030a0001c0001t0001g0209a0001c0001t0002g0004others(7): Show | 12 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-698_197-697ins others(1): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913802 | ||||||
| chr19:53913803
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.197-697A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913803 | ||||||
| chr19:53913809
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.197-691G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913809 | ||||||
| chr19:53913817
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197-683A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913817 | ||||||
| chr19:53913827
|
G | A | 10 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-673G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913827 | ||||||
| chr19:53913879
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(6): Show | 11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-621C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913879 | ||||||
| chr19:53913925
|
A | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(18): Show | 22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-575A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913925 | ||||||
| chr19:53913929
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-571C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913929 | ||||||
| chr19:53914048
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-452G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914048 | ||||||
| chr19:53914064
|
A | T | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-436A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914064 | ||||||
| chr19:53914102
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0338a0001c0001t0002g0178 | 4 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-398C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914102 | ||||||
| chr19:53914110
|
C | A | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 8 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-390C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914110 | ||||||
| chr19:53914205
|
T | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.197-295T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914205 | ||||||
| chr19:53914273
|
C | CAAAAAA | 22 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0033others(19): Show | 25 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-218_197-213dup others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914273 | |||||
| chr19:53914273
|
C | CAAAAAAA | 63 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp2 HG00609.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.197-219_197-213dup others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914273 | |||||
| chr19:53914284
|
AAAAG | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(41): Show | 45 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-212_197-209del others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914284 | |||||
| chr19:53914288
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(18): Show | 22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-212G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914288 | ||||||
| chr19:53914290
|
A | AAAAG | 10 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-207_197-206ins others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914290 | |||||
| chr19:53914290
|
A | AAGAAAAA others(1): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 11 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-209_197-208ins others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914290 | |||||
| chr19:53914290
|
A | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(41): Show | 45 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-210A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914290 | ||||||
| chr19:53914296
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.197-204G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914296 | ||||||
| chr19:53914341
|
G | A | 17 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(14): Show | 18 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.197-159G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914341 | ||||||
| chr19:53914604
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+18C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914604 | ||||||
| chr19:53914692
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.283+106G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914692 | ||||||
| chr19:53914801
|
A | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(52): Show | 57 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.283+215A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914801 | ||||||
| chr19:53914802
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(62): Show | 67 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+216A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914802 | ||||||
| chr19:53914995
|
G | C | 7 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0003g0023others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-370G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914995 | ||||||
| chr19:53915005
|
C | CA | 13 | a0001c0001t0001g0059a0001c0001t0001g0115a0001c0001t0001g0205others(10): Show | 13 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-349dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915005 | |||||
| chr19:53915005
|
C | CAAA | 7 | a0001c0001t0002g0004a0001c0001t0003g0003a0001c0001t0003g0026others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-351_284-349dup others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915005 | |||||
| chr19:53915013
|
A | T | 7 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0087others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-352A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915013 | ||||||
| chr19:53915015
|
AAT | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0093others(43): Show | 47 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.284-348_284-347del others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915015 | |||||
| chr19:53915016
|
AT | A | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0355others(2): Show | 5 | HG02615.hp1 HG02738.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-348delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915016 | ||||||
| chr19:53915017
|
T | A | 10 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-348T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915017 | ||||||
| chr19:53915021
|
T | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0093others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-344T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915021 | ||||||
| chr19:53915031
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0093others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-334G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915031 | ||||||
| chr19:53915091
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0313a0001c0001t0001g0338others(2): Show | 6 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-274G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915091 | ||||||
| chr19:53915295
|
G | C | 2 | a0001c0001t0001g0275a0001c0001t0018g0274 | 2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.284-70G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915295 | ||||||
| chr19:53915534
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.424+29G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915534 | ||||||
| chr19:53915716
|
T | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(46): Show | 50 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.424+211T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915716 | ||||||
| chr19:53915846
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.424+341A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915846 | ||||||
| chr19:53915868
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.424+363A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915868 | ||||||
| chr19:53916084
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.424+579G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916084 | ||||||
| chr19:53916139
|
T | G | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0253 | 3 | HG02809.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.424+634T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916139 | ||||||
| chr19:53916285
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(16): Show | 19 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+780C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916285 | ||||||
| chr19:53916342
|
GGTACCAA others(31): Show |
G | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(125): Show | 133 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.424+873_424+910del others(38): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916342 | |||||
| chr19:53916487
|
C | CT | 123 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+1002dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | |||||
| chr19:53916487
|
C | CTT | 29 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0051others(26): Show | 31 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+1001_424+1002d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | |||||
| chr19:53916487
|
C | CTTT | 8 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0053others(5): Show | 9 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+1000_424+1002d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | |||||
| chr19:53916487
|
C | CTTTT | 7 | a0001c0001t0001g0207a0001c0001t0003g0023a0001c0001t0003g0024others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+999_424+1002du others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | |||||
| chr19:53916489
|
T | TTC | 45 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(42): Show | 46 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.424+985_424+986ins others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916489 | |||||
| chr19:53916552
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0007g0064a0001c0001t0017g0063 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.424+1047G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916552 | ||||||
| chr19:53916662
|
A | AT | 10 | a0001c0001t0001g0215a0001c0001t0001g0326a0001c0001t0002g0004others(7): Show | 12 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+1174dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | |||||
| chr19:53916662
|
AT | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0049others(22): Show | 26 | HG00639.hp2 HG01069.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+1174delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | |||||
| chr19:53916662
|
ATT | A | 7 | a0001c0001t0001g0207a0001c0001t0003g0023a0001c0001t0003g0024others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+1173_424+1174d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | |||||
| chr19:53916706
|
G | A | 1 | a0001c0001t0012g0223 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.424+1201G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916706 | ||||||
| chr19:53916731
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0007g0064a0001c0001t0017g0063 | 3 | HG01891.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.424+1226C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916731 | ||||||
| chr19:53916792
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+1287G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916792 | ||||||
| chr19:53916798
|
C | CT | 25 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0072others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+1310dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916798 | |||||
| chr19:53916798
|
CT | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0119others(15): Show | 18 | HG00597.hp1 HG01069.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+1310delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916798 | |||||
| chr19:53916866
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.424+1361C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916866 | ||||||
| chr19:53916867
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0338 | 3 | HG01256.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.424+1362G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916867 | ||||||
| chr19:53916921
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.424+1416C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916921 | ||||||
| chr19:53917023
|
C | G | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+1518C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917023 | ||||||
| chr19:53917058
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.424+1553G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917058 | ||||||
| chr19:53917265
|
T | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0069others(65): Show | 69 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.424+1760T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917265 | ||||||
| chr19:53917357
|
G | T | 55 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 58 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.424+1852G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917357 | ||||||
| chr19:53917416
|
C | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0087others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+1911C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917416 | ||||||
| chr19:53917669
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0105others(2): Show | 5 | HG02895.hp1 HG02922.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2164G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917669 | ||||||
| chr19:53917705
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(29): Show | 35 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.424+2200A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917705 | ||||||
| chr19:53917809
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.424+2304T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917809 | ||||||
| chr19:53917815
|
CAG | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 11 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+2313_424+2314d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53917815 | |||||
| chr19:53917824
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+2319G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917824 | ||||||
| chr19:53917887
|
A | T | 1 | a0001c0001t0007g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.424+2382A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917887 | ||||||
| chr19:53917929
|
C | CAAGGTCA others(20): Show |
1 | a0001c0001t0001g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.424+2431_424+2432i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53917929 | |||||
| chr19:53917937
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.424+2432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917937 | ||||||
| chr19:53917952
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(2): Show | 5 | NA18939.hp1 NA18971.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2447G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917952 | ||||||
| chr19:53918031
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.424+2526C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918031 | ||||||
| chr19:53918066
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+2561C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918066 | ||||||
| chr19:53918165
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+2660T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918165 | ||||||
| chr19:53918182
|
G | A | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG00735.hp1 HG01255.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+2677G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918182 | ||||||
| chr19:53918307
|
G | A | 9 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2802G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918307 | ||||||
| chr19:53918510
|
T | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+3005T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918510 | ||||||
| chr19:53918575
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+3070T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918575 | ||||||
| chr19:53918597
|
C | T | 110 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 114 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.424+3092C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918597 | ||||||
| chr19:53918669
|
TGATAGTA others(52): Show |
T | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+3167_424+3225d others(61): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53918669 | |||||
| chr19:53918670
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(45): Show | 50 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.424+3165G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918670 | ||||||
| chr19:53918698
|
G | C | 8 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+3193G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918698 | ||||||
| chr19:53918701
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+3196C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918701 | ||||||
| chr19:53918807
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+3302C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918807 | ||||||
| chr19:53918922
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.424+3417G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918922 | ||||||
| chr19:53919064
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+3559G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919064 | ||||||
| chr19:53919085
|
T | A | 1 | a0001c0001t0002g0317 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.424+3580T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919085 | ||||||
| chr19:53919091
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.424+3586T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919091 | ||||||
| chr19:53919140
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+3635C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919140 | ||||||
| chr19:53919195
|
A | C | 32 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(29): Show | 33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+3690A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919195 | ||||||
| chr19:53919323
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+3818A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919323 | ||||||
| chr19:53919376
|
G | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+3871G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919376 | ||||||
| chr19:53919421
|
CTTGCCCC others(19): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.424+3942_424+3967d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919421 | |||||
| chr19:53919450
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.424+3945G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919450 | ||||||
| chr19:53919483
|
GT | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+3979delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919483 | ||||||
| chr19:53919510
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4005G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919510 | ||||||
| chr19:53919533
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+4028T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919533 | ||||||
| chr19:53919538
|
TCTGGTCA others(519): Show |
T | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4075_424+4600d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919538 | |||||
| chr19:53919554
|
GTTGCCCC others(19): Show |
G | 3 | a0001c0001t0001g0059a0001c0001t0011g0349a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+4075_424+4100d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919554 | |||||
| chr19:53919560
|
C | G | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+4055C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919560 | ||||||
| chr19:53919566
|
T | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(48): Show | 52 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+4061T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919566 | ||||||
| chr19:53919580
|
C | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 120 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.424+4075C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919580 | ||||||
| chr19:53919590
|
G | GC | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+4086dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919590 | |||||
| chr19:53919606
|
G | C | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.424+4101G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919606 | ||||||
| chr19:53919615
|
GGCTGGTC others(280): Show |
G | 4 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4112_424+4398d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919615 | |||||
| chr19:53919616
|
G | GT | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4111_424+4112i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919616 | ||||||
| chr19:53919632
|
C | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4127C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919632 | ||||||
| chr19:53919635
|
G | GT | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4130_424+4131i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919635 | ||||||
| chr19:53919642
|
G | GT | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4137_424+4138i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919642 | ||||||
| chr19:53919647
|
TCATTGGT others(256): Show |
T | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4143_424+4405d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919647 | ||||||
| chr19:53919665
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG00609.hp1 NA18969.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4160C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919665 | ||||||
| chr19:53919675
|
TATTGGTG others(20): Show |
T | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4191_424+4217d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919675 | |||||
| chr19:53919696
|
TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.424+4214_424+4239d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919696 | |||||
| chr19:53919700
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0313a0001c0001t0001g0338others(3): Show | 7 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+4195G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919700 | ||||||
| chr19:53919702
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4197C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919702 | ||||||
| chr19:53919742
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+4237C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919742 | ||||||
| chr19:53919782
|
T | C | 114 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.424+4277T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919782 | ||||||
| chr19:53919836
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+4331G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919836 | ||||||
| chr19:53919851
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.424+4346G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919851 | ||||||
| chr19:53919868
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4363C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919868 | ||||||
| chr19:53919886
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.424+4381T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919886 | ||||||
| chr19:53919904
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4399G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919904 | ||||||
| chr19:53919922
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424+4417T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919922 | ||||||
| chr19:53919931
|
GCCTGGTA others(20): Show |
G | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4428_424+4454d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919931 | |||||
| chr19:53919932
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+4427C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919932 | ||||||
| chr19:53919937
|
TATTGGTG others(312): Show |
T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4446_424+4764d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919937 | |||||
| chr19:53919950
|
G | GT | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 7 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4445_424+4446i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919950 | ||||||
| chr19:53919958
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4453T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919958 | ||||||
| chr19:53919963
|
TC | T | 4 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4459delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919963 | ||||||
| chr19:53919978
|
TCCCCAGG others(20): Show |
T | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4477_424+4503d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919978 | |||||
| chr19:53919978
|
TCCCCAGG others(47): Show |
T | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4477_424+4530d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919978 | |||||
| chr19:53919986
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4481C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919986 | ||||||
| chr19:53919991
|
T | TC | 6 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0073others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4486_424+4487i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919991 | ||||||
| chr19:53920005
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4500C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920005 | ||||||
| chr19:53920022
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4517G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920022 | ||||||
| chr19:53920028
|
C | CTTGCCCC others(45): Show |
1 | a0001c0001t0001g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.424+4548_424+4549i others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920028 | |||||
| chr19:53920028
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0061others(8): Show | 12 | HG00597.hp2 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+4523C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920028 | ||||||
| chr19:53920031
|
G | GT | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4526_424+4527i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920031 | ||||||
| chr19:53920032
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4527C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920032 | ||||||
| chr19:53920034
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4529C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920034 | ||||||
| chr19:53920038
|
G | GT | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0032others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+4533_424+4534i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920038 | ||||||
| chr19:53920038
|
GCTGGTCA others(72): Show |
G | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4560_424+4638d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920038 | |||||
| chr19:53920048
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4543G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920048 | ||||||
| chr19:53920054
|
C | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0030others(10): Show | 15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+4549C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920054 | ||||||
| chr19:53920054
|
CTTGCCCC others(19): Show |
C | 2 | a0001c0001t0001g0066a0001c0001t0001g0285 | 2 | HG02559.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.424+4587_424+4612d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920054 | |||||
| chr19:53920058
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4553C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920058 | ||||||
| chr19:53920060
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+4555C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920060 | ||||||
| chr19:53920064
|
G | GT | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4559_424+4560i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920064 | ||||||
| chr19:53920080
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4575G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920080 | ||||||
| chr19:53920084
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4579C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920084 | ||||||
| chr19:53920090
|
G | GCTGGTCA others(20): Show |
1 | a0001c0001t0002g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+4600_424+4601i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920090 | |||||
| chr19:53920090
|
G | GT | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4585_424+4586i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920090 | ||||||
| chr19:53920101
|
G | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0239 | 2 | HG00733.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.424+4596G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920101 | ||||||
| chr19:53920104
|
G | C | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4599G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920104 | ||||||
| chr19:53920106
|
G | C | 32 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(29): Show | 33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+4601G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920106 | ||||||
| chr19:53920110
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4605C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920110 | ||||||
| chr19:53920117
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0073others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4612C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920117 | ||||||
| chr19:53920131
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4626G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920131 | ||||||
| chr19:53920133
|
C | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(4): Show | 8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+4628C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920133 | ||||||
| chr19:53920137
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4632C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920137 | ||||||
| chr19:53920144
|
T | C | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4639T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920144 | ||||||
| chr19:53920144
|
TCTGGTCA others(99): Show |
T | 2 | a0001c0001t0001g0278a0001c0001t0001g0280 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+4720_424+4825d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920144 | |||||
| chr19:53920164
|
TC | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4663delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920164 | |||||
| chr19:53920172
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0006g0017 | 3 | HG02647.hp1 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4667C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920172 | ||||||
| chr19:53920172
|
CCTGGTAT others(71): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4673_424+4750d others(80): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920172 | |||||
| chr19:53920172
|
CCTGGTAT others(340): Show |
C | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4673_424+5019d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920172 | |||||
| chr19:53920173
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+4668C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920173 | ||||||
| chr19:53920177
|
T | TC | 2 | a0001c0001t0001g0002a0001c0001t0011g0349 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4672_424+4673i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920177 | ||||||
| chr19:53920185
|
G | C | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4680G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920185 | ||||||
| chr19:53920187
|
G | C | 1 | a0001c0001t0011g0349 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+4682G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920187 | ||||||
| chr19:53920203
|
TCATTGGT others(234): Show |
T | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4699_424+4939d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920203 | ||||||
| chr19:53920204
|
CATTGGTG others(900): Show |
C | 1 | a0001c0001t0011g0349 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+4720_424+5626d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920204 | |||||
| chr19:53920218
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4713C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920218 | ||||||
| chr19:53920225
|
CTGGTCAT others(18): Show |
C | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4721_424+4745d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920225 | ||||||
| chr19:53920283
|
T | TC | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(2): Show | 6 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4778_424+4779i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920283 | ||||||
| chr19:53920296
|
GCCCCAGG others(155): Show |
G | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4845_424+5006d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920296 | |||||
| chr19:53920297
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4792C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920297 | ||||||
| chr19:53920303
|
GT | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4799delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920303 | ||||||
| chr19:53920310
|
CATTGGTG others(900): Show |
C | 10 | a0001c0001t0001g0207a0001c0001t0001g0269a0001c0001t0002g0004others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+4845_424+5751d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920310 | |||||
| chr19:53920323
|
G | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01123.hp2 HG01346.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4818G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920323 | ||||||
| chr19:53920323
|
GCCCCAGG others(20): Show |
G | 16 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0211others(13): Show | 17 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+4845_424+4871d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920323 | |||||
| chr19:53920324
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4819C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920324 | ||||||
| chr19:53920326
|
CCAGGTCT others(954): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4842_424+5802d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920326 | |||||
| chr19:53920331
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4826T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920331 | ||||||
| chr19:53920347
|
GTTTCCCC others(820): Show |
G | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+4845_424+5671d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920347 | |||||
| chr19:53920350
|
T | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 94 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.424+4845T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920350 | ||||||
| chr19:53920351
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4846C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920351 | ||||||
| chr19:53920353
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4848C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920353 | ||||||
| chr19:53920374
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4869G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920374 | ||||||
| chr19:53920377
|
G | GT | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4872_424+4873i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920377 | ||||||
| chr19:53920378
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4873C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920378 | ||||||
| chr19:53920380
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4875T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920380 | ||||||
| chr19:53920399
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4894G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920399 | ||||||
| chr19:53920401
|
C | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 7 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+4896C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920401 | ||||||
| chr19:53920405
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4900C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920405 | ||||||
| chr19:53920411
|
GT | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4907delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920411 | ||||||
| chr19:53920411
|
GTCTGGTC others(155): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4907_424+5068d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920411 | ||||||
| chr19:53920423
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+4918G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920423 | ||||||
| chr19:53920428
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02615.hp1 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+4923C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920428 | ||||||
| chr19:53920430
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4925T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920430 | ||||||
| chr19:53920431
|
G | GT | 4 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354others(1): Show | 4 | HG02615.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4926_424+4927i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920431 | ||||||
| chr19:53920432
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4927C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920432 | ||||||
| chr19:53920438
|
G | GT | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4933_424+4934i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920438 | ||||||
| chr19:53920440
|
C | CT | 3 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0015g0031 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+4935_424+4936i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920440 | ||||||
| chr19:53920440
|
C | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.424+4935C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920440 | ||||||
| chr19:53920442
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0004g0354 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.424+4937G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920442 | ||||||
| chr19:53920456
|
C | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(7): Show | 10 | HG00438.hp2 HG00544.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4951C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920456 | ||||||
| chr19:53920457
|
GT | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0073others(2): Show | 5 | HG02615.hp1 HG03209.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+4953delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920457 | ||||||
| chr19:53920466
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0006g0017 | 3 | HG02647.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4961T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920466 | ||||||
| chr19:53920482
|
G | C | 1 | a0001c0001t0001g0318 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.424+4977G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920482 | ||||||
| chr19:53920486
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4981C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920486 | ||||||
| chr19:53920513
|
C | T | 2 | a0001c0001t0006g0017a0001c0001t0015g0031 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5008C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920513 | ||||||
| chr19:53920539
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+5034C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920539 | ||||||
| chr19:53920545
|
G | GT | 336 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.424+5040_424+5041i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920545 | ||||||
| chr19:53920550
|
TC | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.424+5046delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920550 | ||||||
| chr19:53920556
|
G | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.424+5051G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920556 | ||||||
| chr19:53920561
|
GTTGTCCC others(499): Show |
G | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5060_424+5565d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920561 | |||||
| chr19:53920562
|
T | A | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5057T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920562 | ||||||
| chr19:53920564
|
GT | G | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5060delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920564 | ||||||
| chr19:53920565
|
TCCCCAGG others(46): Show |
T | 2 | a0001c0001t0001g0021a0001c0001t0001g0355 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+5068_424+5120d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920565 | |||||
| chr19:53920573
|
C | A | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5068C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920573 | ||||||
| chr19:53920573
|
C | T | 2 | a0001c0001t0006g0017a0001c0001t0015g0031 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5068C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920573 | ||||||
| chr19:53920584
|
G | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+5079G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920584 | ||||||
| chr19:53920587
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5082G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920587 | ||||||
| chr19:53920593
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5088C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920593 | ||||||
| chr19:53920600
|
T | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5095T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920600 | ||||||
| chr19:53920605
|
T | TC | 9 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5100_424+5101i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920605 | ||||||
| chr19:53920618
|
G | GT | 3 | a0001c0001t0002g0015a0001c0001t0006g0020a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5113_424+5114i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920618 | ||||||
| chr19:53920619
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(1): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5114C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920619 | ||||||
| chr19:53920624
|
G | A | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5119G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920624 | ||||||
| chr19:53920626
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5121T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920626 | ||||||
| chr19:53920640
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5135G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920640 | ||||||
| chr19:53920646
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5141C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920646 | ||||||
| chr19:53920651
|
GGCTGGTC others(72): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5148_424+5226d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920651 | |||||
| chr19:53920652
|
G | GT | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5147_424+5148i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920652 | ||||||
| chr19:53920672
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5167C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920672 | ||||||
| chr19:53920678
|
GT | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5174delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920678 | ||||||
| chr19:53920679
|
T | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5174T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920679 | ||||||
| chr19:53920684
|
TC | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5180delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920684 | ||||||
| chr19:53920695
|
C | G | 15 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0061others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5190C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920695 | ||||||
| chr19:53920695
|
CTTGCTCC others(552): Show |
C | 29 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(26): Show | 30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+5195_424+5753d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920695 | |||||
| chr19:53920697
|
T | C | 3 | a0001c0001t0003g0003a0001c0001t0003g0027a0001c0001t0008g0025 | 3 | HG01884.hp2 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.424+5192T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920697 | ||||||
| chr19:53920698
|
G | GT | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5193_424+5194i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920698 | ||||||
| chr19:53920698
|
GCTCCAGG others(955): Show |
G | 2 | a0001c0001t0003g0003a0001c0001t0003g0027 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+5194_424+6155d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920698 | ||||||
| chr19:53920699
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5194C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920699 | ||||||
| chr19:53920700
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(79): Show | 83 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.424+5195T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920700 | ||||||
| chr19:53920706
|
T | A | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5201T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920706 | ||||||
| chr19:53920706
|
TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.424+5218_424+5243d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920706 | |||||
| chr19:53920711
|
TC | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5207delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920711 | ||||||
| chr19:53920720
|
G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0355a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5215G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920720 | ||||||
| chr19:53920723
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5218C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920723 | ||||||
| chr19:53920723
|
C | T | 10 | a0001c0001t0001g0021a0001c0001t0001g0335a0001c0001t0001g0355others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5218C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920723 | ||||||
| chr19:53920726
|
T | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0335a0001c0001t0001g0355others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+5221T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920726 | ||||||
| chr19:53920726
|
TCCCAGGC others(18): Show |
T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5225_424+5249d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920726 | |||||
| chr19:53920728
|
C | T | 2 | a0001c0001t0001g0335a0001c0001t0002g0316 | 2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5223C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920728 | ||||||
| chr19:53920732
|
G | GT | 9 | a0001c0001t0001g0021a0001c0001t0001g0335a0001c0001t0001g0355others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+5227_424+5228i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | ||||||
| chr19:53920732
|
G | GTCTGGTC others(75): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5227_424+5228i others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | ||||||
| chr19:53920732
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018 | 4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5227G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | ||||||
| chr19:53920744
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5239T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920744 | ||||||
| chr19:53920748
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5243G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920748 | ||||||
| chr19:53920752
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5247C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920752 | ||||||
| chr19:53920754
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5249C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920754 | ||||||
| chr19:53920758
|
G | T | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5253G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920758 | ||||||
| chr19:53920759
|
T | TCTGGTCA others(18): Show |
1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+5267_424+5268i others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | |||||
| chr19:53920759
|
T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+5269_424+5270i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | |||||
| chr19:53920759
|
T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0201 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.424+5270_424+5295d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | |||||
| chr19:53920775
|
G | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0239a0001c0001t0001g0335 | 3 | HG01243.hp1 HG01496.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.424+5270G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920775 | ||||||
| chr19:53920775
|
G | GTTGCCCC others(19): Show |
80 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 82 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.424+5296_424+5321d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920775 | |||||
| chr19:53920778
|
G | GT | 15 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+5273_424+5274i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920778 | ||||||
| chr19:53920779
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5274C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920779 | ||||||
| chr19:53920785
|
G | GC | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5281dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920785 | |||||
| chr19:53920785
|
G | GT | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5280_424+5281i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920785 | ||||||
| chr19:53920790
|
TC | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5286delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920790 | ||||||
| chr19:53920795
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.424+5290G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920795 | ||||||
| chr19:53920801
|
C | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(6): Show | 9 | HG01496.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5296C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920801 | ||||||
| chr19:53920802
|
T | TCGTCCCC others(289): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5297_424+5298i others(298): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920802 | ||||||
| chr19:53920805
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0335 | 3 | HG01496.hp2 HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+5300C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920805 | ||||||
| chr19:53920808
|
C | CA | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5304dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920808 | |||||
| chr19:53920811
|
G | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5306G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920811 | ||||||
| chr19:53920816
|
TC | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5312delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920816 | ||||||
| chr19:53920822
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5317G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920822 | ||||||
| chr19:53920827
|
G | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(16): Show | 20 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+5322G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920827 | ||||||
| chr19:53920828
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5323T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920828 | ||||||
| chr19:53920830
|
GT | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(17): Show | 21 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+5326delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920830 | ||||||
| chr19:53920831
|
TC | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0192a0001c0001t0006g0017others(1): Show | 4 | HG02647.hp1 NA18972.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5330delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920831 | |||||
| chr19:53920838
|
GC | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5335delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920838 | |||||
| chr19:53920839
|
C | T | 2 | a0001c0001t0006g0017a0001c0001t0015g0031 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5334C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920839 | ||||||
| chr19:53920844
|
T | TC | 28 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(25): Show | 29 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+5339_424+5340i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920844 | ||||||
| chr19:53920852
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5347G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920852 | ||||||
| chr19:53920854
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5349G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920854 | ||||||
| chr19:53920857
|
G | GT | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(9): Show | 12 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5352_424+5353i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920857 | ||||||
| chr19:53920858
|
C | T | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5353C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920858 | ||||||
| chr19:53920865
|
T | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0032others(14): Show | 17 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+5360T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920865 | ||||||
| chr19:53920865
|
T | TCTGGTAT others(45): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5365_424+5366i others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920865 | |||||
| chr19:53920870
|
TC | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(8): Show | 11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5366delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920870 | ||||||
| chr19:53920881
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5376G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920881 | ||||||
| chr19:53920885
|
T | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(11): Show | 14 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5380T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920885 | ||||||
| chr19:53920885
|
T | TC | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5383dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920885 | |||||
| chr19:53920892
|
T | C | 2 | a0001c0001t0001g0335a0001c0001t0008g0025 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.424+5387T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920892 | ||||||
| chr19:53920894
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.424+5389T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920894 | ||||||
| chr19:53920906
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5401G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920906 | ||||||
| chr19:53920910
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5405T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920910 | ||||||
| chr19:53920911
|
GT | G | 3 | a0001c0001t0001g0227a0001c0001t0008g0025a0001c0001t0015g0031 | 3 | HG02145.hp1 NA19007.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5407delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920911 | ||||||
| chr19:53920912
|
TC | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(8): Show | 11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5411delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920912 | |||||
| chr19:53920912
|
TCCCCAGG others(392): Show |
T | 2 | a0001c0001t0001g0002a0001c0001t0001g0018 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5457_424+5855d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920912 | |||||
| chr19:53920915
|
C | T | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5410C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920915 | ||||||
| chr19:53920920
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5415T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920920 | ||||||
| chr19:53920920
|
T | TCTGGTCA others(19): Show |
1 | a0001c0001t0023g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.424+5457_424+5482d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | |||||
| chr19:53920920
|
TCTGGTCA others(19): Show |
T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0002g0342others(1): Show | 4 | HG00323.hp2 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5457_424+5482d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | |||||
| chr19:53920920
|
TCTGGTCA others(45): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5431_424+5482d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | |||||
| chr19:53920936
|
C | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+5431C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920936 | ||||||
| chr19:53920939
|
G | GT | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(8): Show | 11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5434_424+5435i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920939 | ||||||
| chr19:53920940
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0335 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5435C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920940 | ||||||
| chr19:53920942
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5437C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920942 | ||||||
| chr19:53920946
|
G | GT | 14 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(11): Show | 14 | HG02040.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5441_424+5442i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920946 | ||||||
| chr19:53920962
|
C | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(13): Show | 16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+5457C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920962 | ||||||
| chr19:53920962
|
CTTGCCCC others(19): Show |
C | 11 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0072others(8): Show | 11 | HG00673.hp1 HG01109.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+5521_424+5546d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920962 | |||||
| chr19:53920963
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5458T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920963 | ||||||
| chr19:53920964
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5459T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920964 | ||||||
| chr19:53920965
|
G | GT | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5460_424+5461i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920965 | ||||||
| chr19:53920966
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.424+5461C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920966 | ||||||
| chr19:53920966
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0002g0316others(1): Show | 4 | HG02451.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5461C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920966 | ||||||
| chr19:53920972
|
G | GC | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5468dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920972 | |||||
| chr19:53920972
|
G | GCTGGTCA others(48): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5483_424+5484i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920972 | |||||
| chr19:53920972
|
G | GT | 3 | a0001c0001t0001g0032a0001c0001t0001g0335a0001c0001t0015g0031 | 3 | HG01496.hp2 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5467_424+5468i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920972 | ||||||
| chr19:53920973
|
CTGGTCAT others(258): Show |
C | 1 | a0001c0001t0006g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5469_424+5733d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920973 | ||||||
| chr19:53920976
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920976 | ||||||
| chr19:53920986
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5481G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920986 | ||||||
| chr19:53920988
|
G | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0022others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.424+5483G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920988 | ||||||
| chr19:53920992
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5487C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920992 | ||||||
| chr19:53920998
|
G | GT | 13 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+5493_424+5494i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920998 | ||||||
| chr19:53920998
|
GCTGGTCA others(73): Show |
G | 2 | a0001c0001t0001g0105a0001c0001t0001g0179 | 2 | NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.424+5513_424+5592d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920998 | |||||
| chr19:53921002
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5497G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921002 | ||||||
| chr19:53921002
|
G | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5497G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921002 | ||||||
| chr19:53921003
|
TC | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5499delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921003 | ||||||
| chr19:53921014
|
G | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0089others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5509G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921014 | ||||||
| chr19:53921017
|
G | GT | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5512_424+5513i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921017 | ||||||
| chr19:53921024
|
G | GC | 6 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5520dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921024 | |||||
| chr19:53921024
|
G | GT | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+5519_424+5520i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921024 | ||||||
| chr19:53921026
|
T | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5521T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921026 | ||||||
| chr19:53921028
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5523G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921028 | ||||||
| chr19:53921028
|
G | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(10): Show | 13 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+5523G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921028 | ||||||
| chr19:53921031
|
A | G | 6 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5526A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921031 | ||||||
| chr19:53921038
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0335 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5533G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921038 | ||||||
| chr19:53921040
|
G | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5535G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921040 | ||||||
| chr19:53921043
|
G | GT | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5538_424+5539i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921043 | ||||||
| chr19:53921043
|
GCCCCAGG others(989): Show |
G | 1 | a0001c0001t0002g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+5552_424+6547d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921043 | |||||
| chr19:53921044
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5539C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921044 | ||||||
| chr19:53921051
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(16): Show | 19 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.424+5546C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921051 | ||||||
| chr19:53921056
|
TC | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+5552delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921056 | ||||||
| chr19:53921058
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0089 | 3 | HG01109.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+5553A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921058 | ||||||
| chr19:53921062
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5557G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921062 | ||||||
| chr19:53921065
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5560G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921065 | ||||||
| chr19:53921067
|
C | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(18): Show | 21 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+5562C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921067 | ||||||
| chr19:53921070
|
G | GT | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(13): Show | 16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+5565_424+5566i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921070 | ||||||
| chr19:53921078
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+5573T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921078 | ||||||
| chr19:53921083
|
TC | T | 11 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(8): Show | 11 | HG02080.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+5579delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921083 | ||||||
| chr19:53921089
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5584G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921089 | ||||||
| chr19:53921091
|
G | A | 1 | a0001c0001t0021g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.424+5586G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921091 | ||||||
| chr19:53921092
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5587G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921092 | ||||||
| chr19:53921092
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5587G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921092 | ||||||
| chr19:53921094
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5589G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921094 | ||||||
| chr19:53921097
|
G | GCCCCAGG others(69): Show |
1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5592_424+5593i others(78): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921097 | ||||||
| chr19:53921097
|
GT | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5593delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921097 | ||||||
| chr19:53921098
|
T | G | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5593T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921098 | ||||||
| chr19:53921098
|
TCCCCAGG others(125): Show |
T | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5601_424+5732d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921098 | |||||
| chr19:53921106
|
C | CCTGGTAT others(19): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG00609.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.424+5607_424+5632d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921106 | |||||
| chr19:53921106
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5601C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921106 | ||||||
| chr19:53921108
|
T | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5603T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921108 | ||||||
| chr19:53921111
|
T | TATTGGTG others(20): Show |
3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0089 | 3 | HG01109.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+5627_424+5653d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921111 | |||||
| chr19:53921111
|
T | TC | 10 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0087others(7): Show | 10 | HG01496.hp2 HG01891.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5606_424+5607i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921111 | ||||||
| chr19:53921122
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.424+5617T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921122 | ||||||
| chr19:53921123
|
T | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5618T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921123 | ||||||
| chr19:53921125
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5620C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921125 | ||||||
| chr19:53921132
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5627T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921132 | ||||||
| chr19:53921132
|
T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.424+5643_424+5668d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921132 | |||||
| chr19:53921138
|
CATTGGTG others(72): Show |
C | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0105others(1): Show | 4 | HG01243.hp2 HG02717.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5654_424+5732d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921138 | |||||
| chr19:53921146
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5641G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921146 | ||||||
| chr19:53921148
|
GTTGCCCC others(19): Show |
G | 2 | a0001c0001t0001g0008a0001c0001t0004g0354 | 2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5669_424+5694d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921148 | |||||
| chr19:53921152
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0335 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5647C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921152 | ||||||
| chr19:53921158
|
G | GT | 4 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0258others(1): Show | 4 | HG01891.hp1 HG02080.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5653_424+5654i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921158 | ||||||
| chr19:53921158
|
GCTGGTCA others(73): Show |
G | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+5669_424+5748d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921158 | |||||
| chr19:53921159
|
CTGGTCAT others(18): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5655_424+5679d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921159 | ||||||
| chr19:53921174
|
C | G | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(7): Show | 10 | HG00642.hp1 HG01109.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5669C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921174 | ||||||
| chr19:53921178
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5673C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921178 | ||||||
| chr19:53921184
|
G | GT | 5 | a0001c0001t0001g0021a0001c0001t0001g0335a0001c0001t0002g0015others(2): Show | 5 | HG01109.hp1 HG01496.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5679_424+5680i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921184 | ||||||
| chr19:53921190
|
CATTGGTG others(20): Show |
C | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5699_424+5725d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921190 | |||||
| chr19:53921200
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5695G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921200 | ||||||
| chr19:53921200
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5695G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921200 | ||||||
| chr19:53921202
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 4 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5697T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921202 | ||||||
| chr19:53921203
|
GT | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0209a0001c0001t0002g0302others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5699delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921203 | ||||||
| chr19:53921204
|
TCCCCAGG others(100): Show |
T | 4 | a0001c0001t0001g0021a0001c0001t0002g0015a0001c0001t0006g0020others(1): Show | 4 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5707_424+5813d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921204 | |||||
| chr19:53921212
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0209a0001c0001t0001g0335others(1): Show | 4 | HG00642.hp1 HG01496.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5707C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921212 | ||||||
| chr19:53921213
|
C | G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5708C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921213 | ||||||
| chr19:53921217
|
T | TATTGGTG others(20): Show |
170 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(167): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.424+5755_424+5781d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921217 | |||||
| chr19:53921217
|
T | TC | 6 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0335others(3): Show | 6 | HG00642.hp1 HG01496.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5712_424+5713i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921217 | ||||||
| chr19:53921222
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5717G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921222 | ||||||
| chr19:53921230
|
G | GT | 3 | a0001c0001t0001g0032a0001c0001t0001g0209a0001c0001t0008g0025 | 3 | HG01891.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+5725_424+5726i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921230 | ||||||
| chr19:53921231
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0335a0001c0001t0002g0316 | 3 | HG01496.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5726C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921231 | ||||||
| chr19:53921237
|
GT | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0335 | 3 | HG01243.hp2 HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.424+5733delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921237 | ||||||
| chr19:53921238
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0209a0001c0001t0008g0025 | 3 | HG01891.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+5733T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921238 | ||||||
| chr19:53921254
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5749G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921254 | ||||||
| chr19:53921257
|
G | GT | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5752_424+5753i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921257 | ||||||
| chr19:53921258
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0002g0316 | 3 | HG01891.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5753C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921258 | ||||||
| chr19:53921265
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5760T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921265 | ||||||
| chr19:53921283
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0355 | 3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5778T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921283 | ||||||
| chr19:53921284
|
G | GT | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0006g0017others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5779_424+5780i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921284 | ||||||
| chr19:53921284
|
GCCTCAGG others(19): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0355 | 3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5780_424+5805d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921284 | ||||||
| chr19:53921285
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5780C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921285 | ||||||
| chr19:53921287
|
T | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0032others(23): Show | 26 | HG00280.hp2 HG01109.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+5782T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921287 | ||||||
| chr19:53921292
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5787T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921292 | ||||||
| chr19:53921298
|
C | A | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5793C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921298 | ||||||
| chr19:53921301
|
T | TGGTGCAG others(101): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5800_424+5801i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921301 | |||||
| chr19:53921304
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(27): Show | 31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+5799T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921304 | ||||||
| chr19:53921308
|
C | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0032others(15): Show | 18 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+5803C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921308 | ||||||
| chr19:53921311
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0355 | 3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5806G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921311 | ||||||
| chr19:53921312
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5807C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921312 | ||||||
| chr19:53921314
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0210others(3): Show | 6 | HG00280.hp2 HG01993.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5809C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921314 | ||||||
| chr19:53921319
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0066others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5814T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921319 | ||||||
| chr19:53921335
|
C | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+5830C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921335 | ||||||
| chr19:53921335
|
CTTGCCCC others(47): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5841_424+5894d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921335 | |||||
| chr19:53921339
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921339 | ||||||
| chr19:53921343
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5838A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921343 | ||||||
| chr19:53921345
|
G | GT | 7 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0210others(4): Show | 7 | HG00280.hp2 HG01496.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+5840_424+5841i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921345 | ||||||
| chr19:53921361
|
G | C | 5 | a0001c0001t0001g0059a0001c0001t0001g0210a0001c0001t0001g0286others(2): Show | 5 | HG00280.hp2 HG01993.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5856G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921361 | ||||||
| chr19:53921362
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.424+5857T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921362 | ||||||
| chr19:53921363
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(11): Show | 14 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5858C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921363 | ||||||
| chr19:53921364
|
GT | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 12 | HG00280.hp2 HG01891.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5860delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921364 | ||||||
| chr19:53921372
|
GT | G | 4 | a0001c0001t0001g0210a0001c0001t0001g0286a0001c0001t0001g0309others(1): Show | 4 | HG00280.hp2 HG01993.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5868delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921372 | ||||||
| chr19:53921373
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5868T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921373 | ||||||
| chr19:53921389
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5884G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921389 | ||||||
| chr19:53921390
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5885T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921390 | ||||||
| chr19:53921391
|
T | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0286a0001c0001t0001g0309 | 3 | HG00280.hp2 HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.424+5886T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921391 | ||||||
| chr19:53921392
|
G | GT | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0209others(4): Show | 7 | HG00280.hp2 HG01993.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5887_424+5888i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921392 | ||||||
| chr19:53921393
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0335a0001c0001t0002g0316 | 3 | HG01496.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5888C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921393 | ||||||
| chr19:53921395
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0062others(91): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.424+5890C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921395 | ||||||
| chr19:53921399
|
GT | G | 3 | a0001c0001t0001g0059a0001c0001t0008g0025a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5895delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921399 | ||||||
| chr19:53921400
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5895T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921400 | ||||||
| chr19:53921400
|
TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+5922_424+5947d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921400 | |||||
| chr19:53921414
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5909G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921414 | ||||||
| chr19:53921416
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5911G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921416 | ||||||
| chr19:53921418
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5913T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921418 | ||||||
| chr19:53921419
|
G | GT | 3 | a0001c0001t0001g0059a0001c0001t0001g0209a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5914_424+5915i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921419 | ||||||
| chr19:53921420
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5915C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921420 | ||||||
| chr19:53921426
|
G | GT | 19 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(16): Show | 20 | HG00280.hp2 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+5921_424+5922i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921426 | ||||||
| chr19:53921428
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5923T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921428 | ||||||
| chr19:53921442
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5937G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921442 | ||||||
| chr19:53921445
|
GCCCCAGG others(20): Show |
G | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5948_424+5974d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921445 | |||||
| chr19:53921446
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0002g0316 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5941C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921446 | ||||||
| chr19:53921448
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5943C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921448 | ||||||
| chr19:53921451
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5946G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921451 | ||||||
| chr19:53921452
|
GT | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0286a0001c0001t0001g0309 | 3 | HG00280.hp2 HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.424+5948delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921452 | ||||||
| chr19:53921453
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5948T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921453 | ||||||
| chr19:53921453
|
TCTGGTAT others(99): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5954_424+6059d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921453 | |||||
| chr19:53921458
|
T | TC | 11 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(8): Show | 11 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5953_424+5954i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921458 | ||||||
| chr19:53921458
|
TATTGCTG others(21): Show |
T | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5958_424+5985d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921458 | |||||
| chr19:53921458
|
TATTGCTG others(46): Show |
T | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5954_424+6006d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921458 | ||||||
| chr19:53921463
|
C | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 12 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5958C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921463 | ||||||
| chr19:53921466
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5961G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921466 | ||||||
| chr19:53921471
|
GT | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0210others(3): Show | 6 | HG00280.hp2 HG01891.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5967delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921471 | ||||||
| chr19:53921480
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0335 | 3 | HG01496.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+5975C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921480 | ||||||
| chr19:53921494
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0284others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5989G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921494 | ||||||
| chr19:53921494
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5989G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921494 | ||||||
| chr19:53921500
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0002g0316 | 3 | HG01891.hp1 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+5995C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921500 | ||||||
| chr19:53921507
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0209 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6002T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921507 | ||||||
| chr19:53921512
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6007T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921512 | ||||||
| chr19:53921512
|
T | TATTGGTG others(20): Show |
2 | a0001c0001t0001g0036a0001c0001t0002g0162 | 2 | HG01168.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.424+6028_424+6054d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921512 | |||||
| chr19:53921512
|
T | TC | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0209others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6007_424+6008i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921512 | ||||||
| chr19:53921515
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6010T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921515 | ||||||
| chr19:53921517
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6012G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921517 | ||||||
| chr19:53921524
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6019T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921524 | ||||||
| chr19:53921525
|
G | GT | 4 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0209others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6020_424+6021i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921525 | ||||||
| chr19:53921526
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6021C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921526 | ||||||
| chr19:53921526
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6021C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921526 | ||||||
| chr19:53921528
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6023C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921528 | ||||||
| chr19:53921532
|
GT | G | 5 | a0001c0001t0001g0210a0001c0001t0001g0286a0001c0001t0001g0309others(2): Show | 5 | HG00280.hp2 HG01496.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6028delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921532 | ||||||
| chr19:53921533
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0019g0281 | 3 | HG01891.hp1 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6028T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921533 | ||||||
| chr19:53921533
|
T | TCTGGTCA others(19): Show |
7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+6055_424+6080d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921533 | |||||
| chr19:53921549
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6044G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921549 | ||||||
| chr19:53921550
|
T | TC | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6045_424+6046i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921550 | ||||||
| chr19:53921551
|
T | G | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6046T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921551 | ||||||
| chr19:53921552
|
GCCCCAGG others(128): Show |
G | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6048_424+6182d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921552 | ||||||
| chr19:53921553
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG01891.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6048C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921553 | ||||||
| chr19:53921553
|
CCCCAGGC others(156): Show |
C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6087_424+6249d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921553 | |||||
| chr19:53921559
|
G | GCTGGTCA others(20): Show |
4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG00408.hp1 NA18957.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6072_424+6098d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921559 | |||||
| chr19:53921559
|
G | GT | 7 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0210others(4): Show | 7 | HG00280.hp2 HG01993.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+6054_424+6055i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921559 | ||||||
| chr19:53921559
|
GCTGGTCA others(20): Show |
G | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6072_424+6098d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921559 | |||||
| chr19:53921575
|
G | GTCGGCCC others(49): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6071_424+6072i others(58): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921575 | |||||
| chr19:53921575
|
GTTGCCCC others(76): Show |
G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6097_424+6179d others(85): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921575 | |||||
| chr19:53921576
|
T | TC | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 13 | HG02055.hp1 HG02056.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6071_424+6072i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921576 | ||||||
| chr19:53921577
|
T | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 13 | HG02055.hp1 HG02056.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6072T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921577 | ||||||
| chr19:53921579
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0002g0316 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6074C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921579 | ||||||
| chr19:53921585
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6080G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921585 | ||||||
| chr19:53921586
|
T | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6081T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921586 | ||||||
| chr19:53921604
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG00597.hp1 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+6099C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921604 | ||||||
| chr19:53921605
|
GT | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0278others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6101delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921605 | ||||||
| chr19:53921606
|
T | G | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6101T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921606 | ||||||
| chr19:53921606
|
T | TCCCCAGG others(20): Show |
10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6124_424+6125i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | |||||
| chr19:53921606
|
TCCCCAGG others(48): Show |
T | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.424+6125_424+6179d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | |||||
| chr19:53921606
|
TCCCCAGG others(183): Show |
T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+6105_424+6294d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | |||||
| chr19:53921620
|
C | CATTGGTG others(73): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6124_424+6125i others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | |||||
| chr19:53921620
|
C | CATTGGTG others(234): Show |
1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6124_424+6125i others(243): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | |||||
| chr19:53921620
|
C | CATTGGTG others(207): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6124_424+6125i others(216): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | |||||
| chr19:53921628
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.424+6123G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921628 | ||||||
| chr19:53921630
|
G | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0210a0001c0001t0001g0251others(8): Show | 11 | HG00280.hp2 HG01070.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6125G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921630 | ||||||
| chr19:53921632
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 45 | HG00280.hp2 HG00597.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+6127C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921632 | ||||||
| chr19:53921633
|
GT | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0030others(15): Show | 18 | HG00280.hp2 HG01070.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6129delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921633 | ||||||
| chr19:53921634
|
T | TCCCAGGC others(341): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6132_424+6133i others(350): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | |||||
| chr19:53921634
|
T | TCCCCAGG others(182): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6142_424+6143i others(191): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | |||||
| chr19:53921634
|
T | TCCCCAGG others(20): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0084 | 2 | NA18961.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.424+6180_424+6206d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | |||||
| chr19:53921641
|
GT | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6137delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921641 | ||||||
| chr19:53921642
|
T | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6137T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921642 | ||||||
| chr19:53921642
|
TCTGGTCA others(207): Show |
T | 8 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(5): Show | 8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6153_424+6366d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921642 | |||||
| chr19:53921656
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+6151G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921656 | ||||||
| chr19:53921658
|
C | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0059others(12): Show | 15 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6153C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921658 | ||||||
| chr19:53921660
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0059others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6155T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921660 | ||||||
| chr19:53921661
|
G | GT | 5 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0059others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6156_424+6157i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921661 | ||||||
| chr19:53921661
|
G | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0027 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6156G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921661 | ||||||
| chr19:53921662
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6157C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921662 | ||||||
| chr19:53921668
|
G | A | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6163G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921668 | ||||||
| chr19:53921669
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0010g0233 | 2 | HG03139.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.424+6164T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921669 | ||||||
| chr19:53921683
|
G | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0072others(2): Show | 5 | HG01109.hp2 HG02451.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6178G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921683 | ||||||
| chr19:53921685
|
C | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0061others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.424+6180C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921685 | ||||||
| chr19:53921688
|
G | GT | 15 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0072others(12): Show | 15 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6183_424+6184i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921688 | ||||||
| chr19:53921688
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6183G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921688 | ||||||
| chr19:53921689
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0002g0316 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+6184C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921689 | ||||||
| chr19:53921691
|
C | T | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6186C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921691 | ||||||
| chr19:53921696
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6191T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921696 | ||||||
| chr19:53921696
|
T | TCTGGTCA others(48): Show |
2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6207_424+6208i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921696 | |||||
| chr19:53921702
|
CATTGGTG others(45): Show |
C | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6208_424+6259d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921702 | |||||
| chr19:53921710
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6205G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921710 | ||||||
| chr19:53921712
|
G | C | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 12 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6207G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921712 | ||||||
| chr19:53921713
|
C | G | 1 | a0001c0001t0005g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+6208C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921713 | ||||||
| chr19:53921713
|
C | T | 32 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(29): Show | 33 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+6208C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921713 | ||||||
| chr19:53921716
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 13 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6211T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921716 | ||||||
| chr19:53921716
|
T | TC | 14 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+6214dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921716 | |||||
| chr19:53921722
|
G | GC | 4 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0072others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6218dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921722 | |||||
| chr19:53921722
|
G | GT | 21 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 22 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+6217_424+6218i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921722 | ||||||
| chr19:53921722
|
GCTGGTCA others(290): Show |
G | 33 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0207others(30): Show | 34 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+6237_424+6533d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921722 | |||||
| chr19:53921728
|
CATTGGTG others(343): Show |
C | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0002g0221others(2): Show | 5 | HG02074.hp1 NA18944.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6237_424+6586d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921728 | |||||
| chr19:53921738
|
G | C | 12 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(9): Show | 12 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6233G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921738 | ||||||
| chr19:53921739
|
T | C | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6234T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921739 | ||||||
| chr19:53921741
|
G | GT | 46 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0062others(43): Show | 47 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.424+6236_424+6237i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921741 | ||||||
| chr19:53921741
|
GCCCCAGG others(181): Show |
G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6250_424+6437d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921741 | |||||
| chr19:53921741
|
GCCCCAGG others(316): Show |
G | 19 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0194others(16): Show | 19 | HG01175.hp1 HG02083.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6237_424+6559d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921741 | ||||||
| chr19:53921742
|
C | T | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+6237C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921742 | ||||||
| chr19:53921748
|
GT | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 13 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6244delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921748 | ||||||
| chr19:53921749
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0062others(44): Show | 48 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.424+6244T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921749 | ||||||
| chr19:53921753
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0219 | 2 | HG02738.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6248G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921753 | ||||||
| chr19:53921754
|
T | TATTGGTG others(20): Show |
1 | a0001c0001t0001g0166 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.424+6267_424+6293d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921754 | |||||
| chr19:53921754
|
T | TC | 30 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(27): Show | 31 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6249_424+6250i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921754 | ||||||
| chr19:53921754
|
TATTGGTG others(20): Show |
T | 2 | a0001c0001t0001g0112a0001c0001t0019g0281 | 2 | HG02109.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.424+6267_424+6293d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921754 | |||||
| chr19:53921760
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+6255T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921760 | ||||||
| chr19:53921764
|
G | C | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6259G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921764 | ||||||
| chr19:53921766
|
T | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6261T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921766 | ||||||
| chr19:53921768
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0048others(22): Show | 26 | HG01496.hp2 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.424+6263T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921768 | ||||||
| chr19:53921768
|
T | TC | 11 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0087others(8): Show | 11 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6266dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921768
|
T | TCCCAGGT others(21): Show |
2 | a0001c0001t0001g0278a0001c0001t0001g0280 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+6290_424+6317d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921768
|
T | TCCCCAGG others(427): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6266_424+6267i others(436): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921768
|
TCCCAGGT others(181): Show |
T | 31 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0211others(28): Show | 32 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+6267_424+6454d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921768
|
TCCCAGGT others(208): Show |
T | 1 | a0001c0001t0011g0349 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+6267_424+6481d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921768
|
TCCCAGGT others(344): Show |
T | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+6267_424+6617d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | |||||
| chr19:53921775
|
T | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0087others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6270T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921775 | ||||||
| chr19:53921780
|
TC | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6276delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921780 | ||||||
| chr19:53921790
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.424+6285A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921790 | ||||||
| chr19:53921791
|
G | C | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6286G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921791 | ||||||
| chr19:53921794
|
GT | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0062others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6290delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921794 | ||||||
| chr19:53921795
|
T | TCCCCAGG others(20): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.424+6318_424+6344d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | |||||
| chr19:53921795
|
TC | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6294delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | |||||
| chr19:53921795
|
TCCCCAGG others(21): Show |
T | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.424+6294_424+6321d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | |||||
| chr19:53921803
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0062others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6298T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921803 | ||||||
| chr19:53921817
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0002g0316 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6312G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921817 | ||||||
| chr19:53921820
|
T | C | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6315T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921820 | ||||||
| chr19:53921822
|
G | GT | 14 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(11): Show | 15 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6317_424+6318i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921822 | ||||||
| chr19:53921822
|
GCCCCAGG others(73): Show |
G | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6331_424+6410d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921822 | |||||
| chr19:53921823
|
C | T | 21 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0065others(18): Show | 21 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6318C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921823 | ||||||
| chr19:53921829
|
GT | G | 14 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0192others(11): Show | 14 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+6325delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921829 | ||||||
| chr19:53921829
|
GTCTGGTC others(319): Show |
G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6325_424+6650d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921829 | ||||||
| chr19:53921830
|
T | TCTGGTCA others(48): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6347_424+6348i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921830 | |||||
| chr19:53921830
|
TCTGGTCA others(19): Show |
T | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6375_424+6400d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921830 | |||||
| chr19:53921835
|
TC | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0006g0017 | 3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6331delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921835 | ||||||
| chr19:53921850
|
T | C | 25 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 26 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.424+6345T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921850 | ||||||
| chr19:53921856
|
G | GT | 30 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0048others(27): Show | 31 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6351_424+6352i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921856 | ||||||
| chr19:53921861
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6356T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921861 | ||||||
| chr19:53921861
|
TC | T | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6357delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921861 | ||||||
| chr19:53921862
|
CATTGGTG others(46): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.424+6375_424+6427d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921862 | |||||
| chr19:53921867
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6362G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921867 | ||||||
| chr19:53921872
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6367G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921872 | ||||||
| chr19:53921873
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(5): Show | 8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6368T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921873 | ||||||
| chr19:53921876
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0032others(5): Show | 8 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6371T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921876 | ||||||
| chr19:53921882
|
G | GT | 16 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(13): Show | 16 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6377_424+6378i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921882 | ||||||
| chr19:53921887
|
T | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066 | 3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6382T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921887 | ||||||
| chr19:53921888
|
CATTGGTG others(400): Show |
C | 1 | a0001c0001t0019g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.424+6411_424+6817d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921888 | |||||
| chr19:53921896
|
G | C | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6391G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921896 | ||||||
| chr19:53921901
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.424+6396G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921901 | ||||||
| chr19:53921901
|
GT | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0062others(10): Show | 13 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+6397delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921901 | ||||||
| chr19:53921902
|
TC | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6401delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921902 | |||||
| chr19:53921910
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(6): Show | 9 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6405T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921910 | ||||||
| chr19:53921915
|
T | TC | 20 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(17): Show | 20 | HG01109.hp2 HG01891.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+6410_424+6411i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921915 | ||||||
| chr19:53921923
|
G | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6418G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921923 | ||||||
| chr19:53921928
|
GT | G | 18 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(15): Show | 18 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6424delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921928 | ||||||
| chr19:53921929
|
T | TCCCAGGT others(73): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6427_424+6428i others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921929 | |||||
| chr19:53921929
|
TC | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0069others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6428delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921929 | |||||
| chr19:53921930
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6425C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921930 | ||||||
| chr19:53921932
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6427C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921932 | ||||||
| chr19:53921937
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0095a0001c0001t0001g0251others(6): Show | 9 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921937 | ||||||
| chr19:53921937
|
T | TCTGGTCA others(20): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | NA18950.hp2 NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+6479_424+6505d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921937 | |||||
| chr19:53921951
|
G | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0212 | 3 | HG01109.hp2 HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.424+6446G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921951 | ||||||
| chr19:53921956
|
G | GT | 16 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0168others(13): Show | 16 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+6451_424+6452i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921956 | ||||||
| chr19:53921956
|
GCCCCAGG others(129): Show |
G | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+6538_424+6673d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921956 | |||||
| chr19:53921956
|
GCCCCAGG others(155): Show |
G | 1 | a0001c0001t0001g0344 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.424+6452_424+6613d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921956 | ||||||
| chr19:53921956
|
GCCCCAGG others(346): Show |
G | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.424+6459_424+6811d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921956 | |||||
| chr19:53921957
|
C | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066 | 3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6452C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921957 | ||||||
| chr19:53921959
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066 | 3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6454C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921959 | ||||||
| chr19:53921963
|
GC | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+6460delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921963 | |||||
| chr19:53921964
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0069others(29): Show | 32 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+6459C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921964 | ||||||
| chr19:53921978
|
G | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0027 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6473G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921978 | ||||||
| chr19:53921980
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6475G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921980 | ||||||
| chr19:53921983
|
G | GT | 10 | a0001c0001t0001g0030a0001c0001t0001g0209a0001c0001t0001g0251others(7): Show | 11 | HG01070.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6478_424+6479i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921983 | ||||||
| chr19:53921984
|
C | T | 13 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0192others(10): Show | 13 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6479C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921984 | ||||||
| chr19:53921985
|
C | G | 1 | a0001c0001t0005g0304 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424+6480C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921985 | ||||||
| chr19:53921990
|
GC | G | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6487delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921990 | |||||
| chr19:53921991
|
C | CCTGGTCA others(21): Show |
1 | a0001c0001t0001g0124 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.424+6514_424+6541d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921991 | |||||
| chr19:53921991
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0030others(15): Show | 19 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6486C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921991 | ||||||
| chr19:53921992
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6487C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921992 | ||||||
| chr19:53921997
|
CATTGGTG others(209): Show |
C | 1 | a0001c0001t0001g0322 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.424+6542_424+6757d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921997 | |||||
| chr19:53922005
|
G | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0027 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6500G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922005 | ||||||
| chr19:53922007
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6502G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922007 | ||||||
| chr19:53922009
|
T | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6504T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922009 | ||||||
| chr19:53922010
|
G | GCCTCAGG others(100): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6505_424+6506i others(109): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922010 | ||||||
| chr19:53922010
|
GT | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(2): Show | 5 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6506delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922010 | ||||||
| chr19:53922011
|
T | G | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6506T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922011 | ||||||
| chr19:53922011
|
TC | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0030others(19): Show | 22 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6510delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922011 | |||||
| chr19:53922011
|
TCCCCAGG others(182): Show |
T | 11 | a0001c0001t0001g0168a0001c0001t0001g0188a0001c0001t0001g0279others(8): Show | 11 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6520_424+6708d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922011 | |||||
| chr19:53922018
|
GT | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0030others(19): Show | 22 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6514delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922018 | ||||||
| chr19:53922019
|
T | C | 4 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0107others(1): Show | 4 | HG01109.hp2 HG03579.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6514T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922019 | ||||||
| chr19:53922020
|
C | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066 | 3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6515C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922020 | ||||||
| chr19:53922024
|
TC | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0007g0067others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6520delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922024 | ||||||
| chr19:53922035
|
G | C | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6530G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922035 | ||||||
| chr19:53922036
|
T | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(26): Show | 30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+6531T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922036 | ||||||
| chr19:53922039
|
TC | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0209others(2): Show | 5 | HG01109.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6538delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | |||||
| chr19:53922039
|
TCCCCAGG others(47): Show |
T | 8 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(5): Show | 8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6538_424+6591d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | |||||
| chr19:53922039
|
TCCCCAGG others(102): Show |
T | 32 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0211others(29): Show | 33 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+6538_424+6646d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | |||||
| chr19:53922046
|
GC | G | 6 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0209others(3): Show | 6 | HG01109.hp2 HG01496.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6543delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922046 | |||||
| chr19:53922047
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0032others(19): Show | 22 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+6542C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922047 | ||||||
| chr19:53922047
|
CCTGGTAT others(19): Show |
C | 30 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0213others(27): Show | 31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6561_424+6586d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922047 | |||||
| chr19:53922052
|
T | TC | 8 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0209others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6547_424+6548i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922052 | ||||||
| chr19:53922052
|
T | TCATTGGT others(20): Show |
1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6547_424+6548i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922052 | ||||||
| chr19:53922062
|
G | GT | 3 | a0001c0001t0001g0062a0001c0001t0001g0098a0001c0001t0010g0233 | 3 | HG02630.hp1 HG03669.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.424+6559dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922062 | |||||
| chr19:53922065
|
G | GT | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0032others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+6560_424+6561i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | ||||||
| chr19:53922065
|
G | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0062others(18): Show | 21 | HG01175.hp1 HG02083.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6560G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | ||||||
| chr19:53922065
|
GCCCCAGG others(46): Show |
G | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6561_424+6613d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | ||||||
| chr19:53922066
|
C | T | 2 | a0001c0001t0002g0317a0001c0001t0002g0342 | 2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.424+6561C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922066 | ||||||
| chr19:53922073
|
T | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0194others(23): Show | 26 | HG01175.hp1 HG01884.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+6568T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922073 | ||||||
| chr19:53922078
|
T | TC | 20 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0069others(17): Show | 20 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+6573_424+6574i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922078 | ||||||
| chr19:53922078
|
TATTGGTG others(21): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.424+6587_424+6614d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922078 | |||||
| chr19:53922083
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6578G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922083 | ||||||
| chr19:53922091
|
GT | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0069others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6587delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922091 | ||||||
| chr19:53922092
|
T | C | 1 | a0001c0001t0002g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+6587T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922092 | ||||||
| chr19:53922092
|
TC | T | 4 | a0001c0001t0001g0124a0001c0001t0003g0003a0001c0001t0003g0027others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6591delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922092 | |||||
| chr19:53922099
|
GC | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(5): Show | 8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6596delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922099 | |||||
| chr19:53922100
|
C | CCTGGTCA others(20): Show |
1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6614_424+6615i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922100 | |||||
| chr19:53922100
|
C | T | 6 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0169others(3): Show | 6 | HG01109.hp2 HG01952.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6595C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922100 | ||||||
| chr19:53922105
|
TCATTGGT others(101): Show |
T | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+6601_424+6708d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922105 | ||||||
| chr19:53922107
|
A | T | 1 | a0001c0001t0002g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+6602A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922107 | ||||||
| chr19:53922119
|
G | GT | 6 | a0001c0001t0001g0107a0001c0001t0001g0207a0001c0001t0002g0316others(3): Show | 6 | HG02818.hp1 HG03195.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6614_424+6615i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922119 | ||||||
| chr19:53922119
|
G | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0344a0001c0001t0007g0067 | 3 | HG02451.hp2 HG03516.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.424+6614G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922119 | ||||||
| chr19:53922120
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6615C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922120 | ||||||
| chr19:53922123
|
C | CAGGTCTG others(234): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6621_424+6622i others(243): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922123 | |||||
| chr19:53922127
|
C | T | 23 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0061others(20): Show | 24 | HG01070.hp2 HG01109.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+6622C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922127 | ||||||
| chr19:53922127
|
CCTGGTCA others(1019): Show |
C | 1 | a0001c0001t0001g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.424+6646_424+7671d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922127 | |||||
| chr19:53922132
|
TC | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315others(6): Show | 9 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6628delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922132 | ||||||
| chr19:53922141
|
GAGTTGTC others(509): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+6646_424+7161d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922141 | |||||
| chr19:53922143
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6638G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922143 | ||||||
| chr19:53922146
|
GT | G | 4 | a0001c0001t0001g0328a0001c0001t0001g0335a0001c0001t0002g0316others(1): Show | 4 | HG01496.hp2 HG02818.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6642delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922146 | ||||||
| chr19:53922147
|
TC | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(12): Show | 15 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6646delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922147 | |||||
| chr19:53922153
|
G | GGCCTGGT others(19): Show |
1 | a0001c0001t0001g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+6649_424+6650i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922153 | |||||
| chr19:53922154
|
GT | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0061others(34): Show | 38 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+6650delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922154 | ||||||
| chr19:53922155
|
T | C | 3 | a0001c0001t0001g0328a0001c0001t0002g0316a0001c0001t0010g0233 | 3 | HG02818.hp1 HG03669.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.424+6650T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922155 | ||||||
| chr19:53922155
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+6650T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922155 | ||||||
| chr19:53922169
|
GAGTTGTC others(101): Show |
G | 3 | a0001c0001t0001g0030a0001c0001t0001g0251a0001c0001t0001g0315 | 3 | HG01993.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.424+6670_424+6777d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922169 | |||||
| chr19:53922171
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6666G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922171 | ||||||
| chr19:53922174
|
GTCCCAGG others(46): Show |
G | 3 | a0001c0001t0003g0003a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG01884.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+6670_424+6722d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922174 | ||||||
| chr19:53922174
|
GTCCCAGG others(74): Show |
G | 1 | a0001c0001t0002g0004 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.424+6670_424+6750d others(83): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922174 | ||||||
| chr19:53922175
|
T | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0335a0001c0001t0001g0344others(2): Show | 5 | HG01496.hp2 HG02647.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6670T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922175 | ||||||
| chr19:53922175
|
T | TC | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6673dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | |||||
| chr19:53922175
|
T | TCCCCAGG others(49): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6673_424+6674i others(58): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | |||||
| chr19:53922175
|
TCCCAGGC others(18): Show |
T | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+6674_424+6698d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | |||||
| chr19:53922181
|
G | GC | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6677dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922181 | |||||
| chr19:53922181
|
G | GT | 3 | a0001c0001t0001g0277a0001c0001t0002g0316a0001c0001t0003g0026 | 3 | HG02647.hp2 HG02818.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.424+6676_424+6677i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922181 | ||||||
| chr19:53922181
|
GCTGGTCA others(20): Show |
G | 1 | a0001c0001t0001g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.424+6682_424+6708d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922181 | |||||
| chr19:53922186
|
TC | T | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6682delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922186 | ||||||
| chr19:53922187
|
C | CATTGGTG others(19): Show |
21 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0106others(18): Show | 21 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6696_424+6721d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922187 | |||||
| chr19:53922195
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6690G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922195 | ||||||
| chr19:53922197
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6692G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922197 | ||||||
| chr19:53922201
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0002g0091a0001c0001t0007g0067others(1): Show | 4 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6696C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922201 | ||||||
| chr19:53922207
|
GT | G | 3 | a0001c0001t0001g0065a0001c0001t0007g0067a0001c0001t0008g0025 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6703delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | ||||||
| chr19:53922207
|
GTCTGGTA others(103): Show |
G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6703_424+6812d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | ||||||
| chr19:53922207
|
GTCTGGTA others(294): Show |
G | 1 | a0001c0001t0002g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.424+6703_424+7003d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | ||||||
| chr19:53922213
|
T | TATTGGTG others(21): Show |
1 | a0001c0001t0001g0161 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+6744_424+6771d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922213 | |||||
| chr19:53922213
|
T | TC | 13 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6708_424+6709i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | ||||||
| chr19:53922213
|
T | TCATTGGT others(47): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6708_424+6709i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | ||||||
| chr19:53922213
|
T | TCATTGGT others(101): Show |
1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6708_424+6709i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | ||||||
| chr19:53922213
|
T | TCATTGGT others(505): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6708_424+6709i others(514): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | ||||||
| chr19:53922213
|
TATTGGTG others(21): Show |
T | 2 | a0001c0001t0001g0168a0001c0001t0001g0341 | 2 | NA18953.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.424+6744_424+6771d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922213 | |||||
| chr19:53922221
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6716G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922221 | ||||||
| chr19:53922226
|
GT | G | 9 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0072others(6): Show | 9 | HG01109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6722delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922226 | ||||||
| chr19:53922227
|
T | G | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6722T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922227 | ||||||
| chr19:53922227
|
TC | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6726delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922227 | |||||
| chr19:53922228
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6723C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922228 | ||||||
| chr19:53922235
|
T | C | 12 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0192others(9): Show | 12 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6730T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922235 | ||||||
| chr19:53922240
|
TC | T | 8 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0179others(5): Show | 8 | HG02145.hp1 HG03669.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6736delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922240 | ||||||
| chr19:53922249
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0066others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6744G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922249 | ||||||
| chr19:53922249
|
G | T | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6744G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922249 | ||||||
| chr19:53922254
|
GT | G | 60 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0066others(57): Show | 61 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.424+6750delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | ||||||
| chr19:53922254
|
GTCCCCAG others(48): Show |
G | 42 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 43 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+6750_424+6804d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | ||||||
| chr19:53922254
|
GTCCCCAG others(132): Show |
G | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6750_424+6888d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | ||||||
| chr19:53922255
|
TC | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0335others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6754delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922255 | |||||
| chr19:53922263
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6758T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922263 | ||||||
| chr19:53922263
|
T | TCTGGTAT others(126): Show |
1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6763_424+6764i others(135): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922263 | |||||
| chr19:53922269
|
CATTGGTG others(19): Show |
C | 3 | a0001c0001t0001g0207a0001c0001t0006g0351a0001c0001t0014g0208 | 3 | HG03195.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.424+6772_424+6797d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922269 | |||||
| chr19:53922277
|
C | G | 16 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0069others(13): Show | 16 | HG01109.hp2 HG01496.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6772C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922277 | ||||||
| chr19:53922277
|
CAGTTGCC others(19): Show |
C | 50 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0213others(47): Show | 51 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.424+6778_424+6803d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922277 | |||||
| chr19:53922277
|
CAGTTGCC others(75): Show |
C | 1 | a0001c0001t0004g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424+6778_424+6859d others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922277 | |||||
| chr19:53922282
|
G | GT | 13 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0105others(10): Show | 13 | HG01070.hp2 HG01109.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6777_424+6778i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922282 | ||||||
| chr19:53922282
|
GCCCCAGG others(20): Show |
G | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6791_424+6817d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922282 | |||||
| chr19:53922283
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0209 | 3 | HG02559.hp2 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6778C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922283 | ||||||
| chr19:53922290
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0003g0026 | 3 | HG02559.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6785T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922290 | ||||||
| chr19:53922292
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.424+6787T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922292 | ||||||
| chr19:53922295
|
T | TC | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00597.hp1 HG01070.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.424+6790_424+6791i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922295 | ||||||
| chr19:53922295
|
T | TCATTGGT others(155): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6790_424+6791i others(164): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922295 | ||||||
| chr19:53922295
|
TATTGGTG others(21): Show |
T | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6812_424+6839d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922295 | |||||
| chr19:53922303
|
G | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(16): Show | 19 | HG00597.hp1 HG01993.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6798G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922303 | ||||||
| chr19:53922308
|
GT | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6804delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922308 | ||||||
| chr19:53922309
|
T | TCCCAGGC others(99): Show |
1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6807_424+6808i others(108): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922309 | |||||
| chr19:53922309
|
TCCCCAGG others(1367): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.424+6808_424+8181d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922309 | |||||
| chr19:53922317
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0002g0004others(3): Show | 6 | HG01070.hp2 HG01884.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+6812T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922317 | ||||||
| chr19:53922317
|
T | TCTGGTCA others(21): Show |
1 | a0001c0001t0002g0321 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+6892_424+6919d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922317 | |||||
| chr19:53922317
|
TCTGGTCA others(21): Show |
T | 30 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(27): Show | 31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6892_424+6919d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922317 | |||||
| chr19:53922321
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6816G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922321 | ||||||
| chr19:53922322
|
TC | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+6818delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922322 | ||||||
| chr19:53922331
|
G | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0022others(40): Show | 44 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.424+6826G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922331 | ||||||
| chr19:53922331
|
G | GAGTTGCC others(20): Show |
2 | a0001c0001t0001g0212a0001c0001t0001g0335 | 2 | HG01496.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+6831_424+6832i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922331 | |||||
| chr19:53922333
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+6828G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922333 | ||||||
| chr19:53922333
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6828G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922333 | ||||||
| chr19:53922336
|
GT | G | 3 | a0001c0001t0001g0238a0001c0001t0015g0031a0001c0001t0019g0281 | 3 | HG02109.hp1 NA20905.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+6832delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922336 | ||||||
| chr19:53922337
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6832T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922337 | ||||||
| chr19:53922337
|
TC | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6836delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922337 | |||||
| chr19:53922340
|
C | CAGGTCTG others(46): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6835_424+6836i others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922340 | ||||||
| chr19:53922345
|
C | T | 56 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0022others(53): Show | 57 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.424+6840C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922345 | ||||||
| chr19:53922350
|
TC | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0010g0233 | 3 | HG01109.hp2 HG03579.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.424+6846delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922350 | ||||||
| chr19:53922359
|
G | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6854G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922359 | ||||||
| chr19:53922361
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6856G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922361 | ||||||
| chr19:53922364
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6859G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922364 | ||||||
| chr19:53922364
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0107others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6860delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922364 | ||||||
| chr19:53922365
|
TC | T | 5 | a0001c0001t0001g0328a0001c0001t0002g0004a0001c0001t0003g0003others(2): Show | 5 | HG01070.hp2 HG01884.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+6864delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922365 | |||||
| chr19:53922373
|
C | T | 13 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0069others(10): Show | 13 | HG01070.hp2 HG01109.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6868C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922373 | ||||||
| chr19:53922373
|
CCTGGTCA others(154): Show |
C | 3 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0179 | 3 | NA18954.hp2 NA19085.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.424+6888_424+7048d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922373 | |||||
| chr19:53922378
|
TC | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0107 | 3 | HG01109.hp2 HG03579.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+6874delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922378 | ||||||
| chr19:53922387
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6882G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922387 | ||||||
| chr19:53922387
|
GAGTTGTC others(263): Show |
G | 3 | a0001c0001t0001g0032a0001c0001t0003g0003a0001c0001t0003g0027 | 3 | HG01884.hp2 HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6892_424+7161d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922387 | |||||
| chr19:53922389
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+6884G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922389 | ||||||
| chr19:53922392
|
GT | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG01884.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+6888delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922392 | ||||||
| chr19:53922393
|
TC | T | 33 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0065others(30): Show | 34 | HG01070.hp2 HG01071.hp1 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+6892delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922393 | |||||
| chr19:53922400
|
GC | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0328others(2): Show | 5 | HG01070.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6897delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922400 | |||||
| chr19:53922401
|
C | T | 32 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0066others(29): Show | 32 | HG01071.hp1 HG01884.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+6896C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922401 | ||||||
| chr19:53922406
|
T | C | 18 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0220others(15): Show | 18 | HG02074.hp1 HG02083.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6901T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922406 | ||||||
| chr19:53922417
|
G | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6912G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922417 | ||||||
| chr19:53922421
|
T | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6916T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922421 | ||||||
| chr19:53922421
|
T | TC | 16 | a0001c0001t0001g0107a0001c0001t0001g0192a0001c0001t0001g0196others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6919dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922421 | |||||
| chr19:53922427
|
GT | G | 28 | a0001c0001t0001g0030a0001c0001t0001g0207a0001c0001t0001g0213others(25): Show | 28 | HG00323.hp1 HG01071.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6923delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922427 | ||||||
| chr19:53922428
|
T | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0210a0001c0001t0002g0167others(4): Show | 7 | HG01993.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6923T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922428 | ||||||
| chr19:53922433
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18747.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.424+6928T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922433 | ||||||
| chr19:53922448
|
T | C | 25 | a0001c0001t0001g0030a0001c0001t0001g0213a0001c0001t0001g0216others(22): Show | 25 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+6943T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922448 | ||||||
| chr19:53922448
|
TCCCAGGC others(19): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6950_424+6975d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922448 | |||||
| chr19:53922454
|
G | GCTGGTCA others(690): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6964_424+6965i others(699): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | |||||
| chr19:53922454
|
G | GT | 30 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0213others(27): Show | 30 | HG01071.hp1 HG01993.hp2 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+6949_424+6950i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922454 | ||||||
| chr19:53922454
|
GCTGGTCA others(20): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.424+6969_424+6995d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | |||||
| chr19:53922454
|
GCTGGTCA others(47): Show |
G | 1 | a0001c0001t0001g0256 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.424+6969_424+7022d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | |||||
| chr19:53922470
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6965G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922470 | ||||||
| chr19:53922470
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6965G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922470 | ||||||
| chr19:53922474
|
C | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0210a0001c0001t0001g0213others(25): Show | 28 | HG01071.hp1 HG01993.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6969C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922474 | ||||||
| chr19:53922479
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+6974G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922479 | ||||||
| chr19:53922480
|
GT | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0328a0001c0001t0002g0004others(3): Show | 6 | HG01071.hp1 HG01993.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6976delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922480 | ||||||
| chr19:53922481
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+6976T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922481 | ||||||
| chr19:53922481
|
TCTGGTCA others(422): Show |
T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.424+7023_424+7451d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922481 | |||||
| chr19:53922486
|
T | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6981T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922486 | ||||||
| chr19:53922486
|
TC | T | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6982delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922486 | ||||||
| chr19:53922487
|
C | T | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6982C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922487 | ||||||
| chr19:53922497
|
G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6992G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922497 | ||||||
| chr19:53922501
|
T | C | 11 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0238others(8): Show | 11 | HG01071.hp1 HG01109.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6996T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922501 | ||||||
| chr19:53922501
|
T | TC | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6999dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | |||||
| chr19:53922501
|
TCCCAGGT others(46): Show |
T | 4 | a0001c0001t0002g0004a0001c0001t0003g0003a0001c0001t0003g0028others(1): Show | 4 | HG01070.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7030_424+7082d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | |||||
| chr19:53922501
|
TCCCAGGT others(287): Show |
T | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7000_424+7293d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | |||||
| chr19:53922507
|
GT | G | 24 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0213others(21): Show | 24 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+7003delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922507 | ||||||
| chr19:53922508
|
TCTGGTCA others(19): Show |
T | 3 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0019g0281 | 3 | HG02109.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.424+7023_424+7048d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922508 | |||||
| chr19:53922522
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7017G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922522 | ||||||
| chr19:53922524
|
G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7019G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922524 | ||||||
| chr19:53922528
|
T | C | 30 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0065others(27): Show | 30 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.424+7023T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922528 | ||||||
| chr19:53922528
|
T | TC | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7026dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922528 | |||||
| chr19:53922532
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+7027A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922532 | ||||||
| chr19:53922534
|
G | GT | 46 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0065others(43): Show | 46 | HG01071.hp1 HG01175.hp1 HG01934.hp1 others(43): Show |
intron_variant | MODIFIER | c.424+7029_424+7030i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922534 | ||||||
| chr19:53922534
|
GCTGGTCA others(396): Show |
G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7103_424+7505d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922534 | |||||
| chr19:53922548
|
G | C | 13 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(10): Show | 13 | HG01071.hp1 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+7043G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922548 | ||||||
| chr19:53922554
|
C | T | 33 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0102others(30): Show | 33 | HG00438.hp2 HG01175.hp1 HG01993.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+7049C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922554 | ||||||
| chr19:53922556
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7051C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922556 | ||||||
| chr19:53922560
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0102others(2): Show | 5 | HG00438.hp2 HG01993.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7056delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922560 | ||||||
| chr19:53922562
|
CTGGTCAT others(397): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7058_424+7461d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922562 | ||||||
| chr19:53922575
|
G | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0119others(42): Show | 45 | HG01070.hp2 HG01175.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+7070G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922575 | ||||||
| chr19:53922575
|
G | T | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7070G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922575 | ||||||
| chr19:53922575
|
GAGTTGTC others(20): Show |
G | 1 | a0001c0001t0002g0004 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.424+7083_424+7109d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922575 | |||||
| chr19:53922579
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7074T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922579 | ||||||
| chr19:53922581
|
T | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0065others(42): Show | 45 | HG01070.hp2 HG01175.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+7076T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922581 | ||||||
| chr19:53922581
|
T | TCCCAGAT others(20): Show |
1 | a0001c0001t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.424+7081_424+7082i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922581 | |||||
| chr19:53922581
|
T | TCCCCAGG others(102): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7079_424+7080i others(111): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922581 | |||||
| chr19:53922582
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7077C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922582 | ||||||
| chr19:53922588
|
A | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0161others(3): Show | 6 | HG01358.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7083A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922588 | ||||||
| chr19:53922588
|
A | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.424+7083A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922588 | ||||||
| chr19:53922588
|
ACTGGTCA others(20): Show |
A | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+7107_424+7133d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922588 | |||||
| chr19:53922593
|
TC | T | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7089delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922593 | ||||||
| chr19:53922602
|
C | CAGTTGCC others(20): Show |
36 | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0088others(33): Show | 37 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+7102_424+7103i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922602 | |||||
| chr19:53922602
|
C | G | 53 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0061others(50): Show | 53 | HG00323.hp1 HG01070.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+7097C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922602 | ||||||
| chr19:53922608
|
T | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 59 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.424+7103T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922608 | ||||||
| chr19:53922608
|
T | TC | 12 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(9): Show | 12 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7106dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | |||||
| chr19:53922608
|
T | TCCCAGGC others(21): Show |
1 | a0001c0001t0001g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.424+7134_424+7161d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | |||||
| chr19:53922608
|
TCCCAGGC others(21): Show |
T | 1 | a0001c0001t0001g0134 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.424+7134_424+7161d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | |||||
| chr19:53922610
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+7105C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922610 | ||||||
| chr19:53922614
|
GC | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0256others(1): Show | 4 | HG00323.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7111delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922614 | |||||
| chr19:53922614
|
GCCTGGTC others(343): Show |
G | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+7111_424+7460d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922614 | |||||
| chr19:53922615
|
C | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG02071.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7110C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922615 | ||||||
| chr19:53922615
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0061others(37): Show | 41 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.424+7110C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922615 | ||||||
| chr19:53922629
|
C | G | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(119): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+7124C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922629 | ||||||
| chr19:53922629
|
CAGTTGTC others(47): Show |
C | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.424+7130_424+7183d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922629 | |||||
| chr19:53922634
|
GT | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0256others(3): Show | 6 | HG00323.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7130delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922634 | ||||||
| chr19:53922635
|
TC | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 55 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.424+7134delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922635 | |||||
| chr19:53922639
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7134C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922639 | ||||||
| chr19:53922643
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0209others(4): Show | 7 | HG00323.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7138C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922643 | ||||||
| chr19:53922648
|
TCATTGGT others(47): Show |
T | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7144_424+7197d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922648 | ||||||
| chr19:53922652
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+7147T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922652 | ||||||
| chr19:53922657
|
C | G | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(119): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+7152C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922657 | ||||||
| chr19:53922659
|
G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7154G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922659 | ||||||
| chr19:53922663
|
T | A | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7158T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922663 | ||||||
| chr19:53922663
|
T | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0210a0001c0001t0001g0328others(3): Show | 6 | HG01993.hp1 HG02451.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7158T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922663 | ||||||
| chr19:53922663
|
T | TC | 51 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 53 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7161dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922663 | |||||
| chr19:53922664
|
CCCAGGCT others(152): Show |
C | 9 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 9 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+7162_424+7320d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922664 | |||||
| chr19:53922665
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7160C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922665 | ||||||
| chr19:53922669
|
G | GC | 51 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 53 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7165dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922669 | |||||
| chr19:53922669
|
G | GT | 7 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0256others(4): Show | 7 | HG00323.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7164_424+7165i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922669 | ||||||
| chr19:53922670
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7165C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922670 | ||||||
| chr19:53922671
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7166T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922671 | ||||||
| chr19:53922681
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+7176T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922681 | ||||||
| chr19:53922683
|
G | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0209a0001c0001t0001g0256 | 3 | HG00323.hp1 HG00438.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.424+7178G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922683 | ||||||
| chr19:53922689
|
C | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+7184C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922689 | ||||||
| chr19:53922695
|
GT | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 52 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+7191delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922695 | ||||||
| chr19:53922696
|
T | C | 2 | a0001c0001t0003g0026a0001c0001t0010g0233 | 2 | HG02647.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.424+7191T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922696 | ||||||
| chr19:53922701
|
TC | T | 3 | a0001c0001t0001g0065a0001c0001t0002g0316a0001c0001t0007g0067 | 3 | HG02451.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+7197delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922701 | ||||||
| chr19:53922705
|
T | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0245others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7200T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922705 | ||||||
| chr19:53922712
|
G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7207G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922712 | ||||||
| chr19:53922715
|
G | GT | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7210_424+7211i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922715 | ||||||
| chr19:53922716
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00323.hp1 HG01891.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+7211C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922716 | ||||||
| chr19:53922718
|
C | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7213C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922718 | ||||||
| chr19:53922720
|
AGGTCTGG others(155): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7217_424+7378d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922720 | |||||
| chr19:53922723
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0238a0001c0001t0001g0256 | 3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7218T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922723 | ||||||
| chr19:53922723
|
TCTGGTCA others(153): Show |
T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7238_424+7397d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922723 | |||||
| chr19:53922726
|
GGTCATTG others(46): Show |
G | 29 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0246others(26): Show | 30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+7238_424+7290d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922726 | |||||
| chr19:53922728
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7224delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922728 | ||||||
| chr19:53922739
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+7234G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922739 | ||||||
| chr19:53922743
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0212others(1): Show | 4 | HG01891.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7238T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922743 | ||||||
| chr19:53922743
|
T | TC | 8 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7241dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922743 | |||||
| chr19:53922743
|
T | TCCCCAGG others(48): Show |
1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7241_424+7242i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922743 | |||||
| chr19:53922750
|
T | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7245T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922750 | ||||||
| chr19:53922753
|
GGTCATTG others(19): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7260_424+7285d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922753 | |||||
| chr19:53922764
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7259G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922764 | ||||||
| chr19:53922765
|
G | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0030others(83): Show | 89 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.424+7260G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922765 | ||||||
| chr19:53922770
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7265T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922770 | ||||||
| chr19:53922770
|
T | TC | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7268dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922770 | |||||
| chr19:53922770
|
TCCCAGGC others(289): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7273_424+7568d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922770 | |||||
| chr19:53922776
|
G | GC | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7272dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922776 | |||||
| chr19:53922776
|
G | GT | 72 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0059others(69): Show | 75 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.424+7271_424+7272i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922776 | ||||||
| chr19:53922779
|
C | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(82): Show | 88 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+7274C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922779 | ||||||
| chr19:53922790
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7285G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922790 | ||||||
| chr19:53922796
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0059others(66): Show | 72 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.424+7291C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922796 | ||||||
| chr19:53922802
|
GT | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0059others(65): Show | 71 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.424+7298delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922802 | ||||||
| chr19:53922803
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7298T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922803 | ||||||
| chr19:53922813
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7308G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922813 | ||||||
| chr19:53922817
|
G | C | 1 | a0001c0001t0001g0352 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7312G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922817 | ||||||
| chr19:53922819
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7314G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922819 | ||||||
| chr19:53922823
|
T | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0059others(72): Show | 78 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.424+7318T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922823 | ||||||
| chr19:53922823
|
T | TC | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7321dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922823 | |||||
| chr19:53922825
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7320C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922825 | ||||||
| chr19:53922829
|
GT | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0212others(1): Show | 4 | HG01109.hp2 HG02647.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7325delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922829 | ||||||
| chr19:53922830
|
T | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7325T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922830 | ||||||
| chr19:53922844
|
C | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(49): Show | 53 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7339C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922844 | ||||||
| chr19:53922849
|
G | GT | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7344_424+7345i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922849 | ||||||
| chr19:53922850
|
C | A | 1 | a0001c0001t0001g0352 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7345C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922850 | ||||||
| chr19:53922850
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0196others(40): Show | 44 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.424+7345C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922850 | ||||||
| chr19:53922852
|
C | T | 1 | a0001c0001t0001g0352 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7347C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922852 | ||||||
| chr19:53922853
|
C | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7348C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922853 | ||||||
| chr19:53922857
|
T | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7352T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922857 | ||||||
| chr19:53922857
|
T | TCTGGTAT others(1547): Show |
1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+7357_424+7358i others(1556): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | |||||
| chr19:53922857
|
T | TCTGGTAT others(597): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7357_424+7358i others(606): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | |||||
| chr19:53922857
|
TCTGGTCA others(19): Show |
T | 2 | a0001c0001t0001g0210a0001c0001t0005g0099 | 2 | HG01993.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.424+7372_424+7397d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | |||||
| chr19:53922862
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7358delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922862 | ||||||
| chr19:53922871
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.424+7366G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922871 | ||||||
| chr19:53922871
|
GAGTTGAC others(154): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7372_424+7532d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922871 | |||||
| chr19:53922873
|
G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7368G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922873 | ||||||
| chr19:53922877
|
A | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+7372A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922877 | ||||||
| chr19:53922877
|
A | T | 42 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0196others(39): Show | 43 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+7372A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922877 | ||||||
| chr19:53922879
|
T | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(48): Show | 52 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+7374T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922879 | ||||||
| chr19:53922879
|
TCAGGCTG others(46): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7379_424+7431d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922879 | |||||
| chr19:53922880
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.424+7375C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922880 | ||||||
| chr19:53922883
|
G | GC | 15 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0272others(12): Show | 15 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.424+7379dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922883 | |||||
| chr19:53922883
|
G | GT | 10 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+7378_424+7379i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922883 | ||||||
| chr19:53922888
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7384delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922888 | ||||||
| chr19:53922898
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7393A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922898 | ||||||
| chr19:53922902
|
G | GT | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7397_424+7398i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922902 | ||||||
| chr19:53922903
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0238others(1): Show | 4 | HG00323.hp1 HG02886.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7398C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922903 | ||||||
| chr19:53922909
|
GC | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0238others(1): Show | 4 | HG00323.hp1 HG01993.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7406delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922909 | |||||
| chr19:53922910
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0072others(44): Show | 48 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.424+7405C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922910 | ||||||
| chr19:53922915
|
T | C | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7410T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922915 | ||||||
| chr19:53922924
|
G | C | 1 | a0001c0001t0003g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7419G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922924 | ||||||
| chr19:53922930
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(79): Show | 85 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.424+7425T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922930 | ||||||
| chr19:53922930
|
TCCCAGGT others(20): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+7452_424+7478d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922930 | |||||
| chr19:53922936
|
GT | G | 3 | a0001c0001t0001g0212a0001c0001t0003g0026a0001c0001t0010g0233 | 3 | HG02647.hp2 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+7432delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922936 | ||||||
| chr19:53922937
|
T | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922937 | ||||||
| chr19:53922937
|
T | TCTGGTCA others(19): Show |
11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7451_424+7452i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922937 | |||||
| chr19:53922944
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.424+7439A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922944 | ||||||
| chr19:53922951
|
G | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7446G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922951 | ||||||
| chr19:53922952
|
AGTTGCCC others(236): Show |
A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7452_424+7694d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922952 | |||||
| chr19:53922956
|
G | GT | 78 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(75): Show | 81 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.424+7451_424+7452i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922956 | ||||||
| chr19:53922957
|
C | A | 1 | a0001c0001t0003g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7452C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922957 | ||||||
| chr19:53922957
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7452C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922957 | ||||||
| chr19:53922959
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7454C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922959 | ||||||
| chr19:53922969
|
TC | T | 66 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(63): Show | 69 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.424+7465delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922969 | ||||||
| chr19:53922978
|
G | A | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7473G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922978 | ||||||
| chr19:53922984
|
T | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7479T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922984 | ||||||
| chr19:53922984
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0003g0024 | 2 | HG03041.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7479T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922984 | ||||||
| chr19:53922984
|
T | TC | 71 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(68): Show | 74 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.424+7482dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | |||||
| chr19:53922984
|
TCCCAGGA others(19): Show |
T | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7483_424+7508d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | |||||
| chr19:53922984
|
TCCCAGGA others(368): Show |
T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+7483_424+7857d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | |||||
| chr19:53922985
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7480C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922985 | ||||||
| chr19:53922986
|
C | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7481C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922986 | ||||||
| chr19:53922990
|
GA | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(34): Show | 38 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+7486delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922990 | ||||||
| chr19:53922991
|
A | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0003g0024 | 3 | HG01109.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7486A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922991 | ||||||
| chr19:53922991
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(82): Show | 89 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.424+7486A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922991 | ||||||
| chr19:53922996
|
TC | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(66): Show | 72 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.424+7492delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922996 | ||||||
| chr19:53923005
|
C | G | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0030others(108): Show | 115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.424+7500C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923005 | ||||||
| chr19:53923007
|
G | GT | 55 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(52): Show | 56 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.424+7504dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923007 | |||||
| chr19:53923010
|
G | GT | 16 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0069others(13): Show | 18 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.424+7505_424+7506i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923010 | ||||||
| chr19:53923010
|
G | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(52): Show | 56 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.424+7505G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923010 | ||||||
| chr19:53923011
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0005g0099 | 2 | HG04115.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7506C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923011 | ||||||
| chr19:53923018
|
C | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0285 | 2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7513C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923018 | ||||||
| chr19:53923018
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(88): Show | 95 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.424+7513C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923018 | ||||||
| chr19:53923023
|
TC | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0061others(70): Show | 76 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.424+7519delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923023 | ||||||
| chr19:53923026
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7521T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923026 | ||||||
| chr19:53923032
|
C | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.424+7527C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923032 | ||||||
| chr19:53923037
|
G | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7532G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923037 | ||||||
| chr19:53923038
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0072others(30): Show | 34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7533T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923038 | ||||||
| chr19:53923038
|
T | TC | 78 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0022others(75): Show | 81 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.424+7536dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923038 | |||||
| chr19:53923041
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0003g0026 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+7536C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923041 | ||||||
| chr19:53923045
|
C | T | 45 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(42): Show | 46 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.424+7540C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923045 | ||||||
| chr19:53923050
|
TC | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+7546delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923050 | ||||||
| chr19:53923059
|
C | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.424+7554C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923059 | ||||||
| chr19:53923064
|
GT | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0245a0001c0001t0001g0335 | 3 | HG01496.hp2 HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7560delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923064 | ||||||
| chr19:53923065
|
TC | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0093others(60): Show | 66 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.424+7564delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923065 | |||||
| chr19:53923073
|
C | T | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(100): Show | 107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.424+7568C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923073 | ||||||
| chr19:53923073
|
CCTGGTCA others(19): Show |
C | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.424+7588_424+7613d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923073 | |||||
| chr19:53923078
|
T | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG02155.hp2 NA18961.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7573T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923078 | ||||||
| chr19:53923078
|
TC | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+7574delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923078 | ||||||
| chr19:53923087
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+7582G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923087 | ||||||
| chr19:53923092
|
G | T | 1 | a0001c0001t0003g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7587G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923092 | ||||||
| chr19:53923093
|
T | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7588T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923093 | ||||||
| chr19:53923093
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(4): Show | 8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7588T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923093 | ||||||
| chr19:53923093
|
T | TC | 33 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0172others(30): Show | 34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7591dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923093 | |||||
| chr19:53923095
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7590C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923095 | ||||||
| chr19:53923099
|
G | GCTGGTCA others(20): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7602_424+7603i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923099 | |||||
| chr19:53923099
|
G | GT | 42 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0069others(39): Show | 43 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+7594_424+7595i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923099 | ||||||
| chr19:53923099
|
GCTGGTCA others(20): Show |
G | 12 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(9): Show | 12 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7641_424+7667d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923099 | |||||
| chr19:53923102
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7597G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923102 | ||||||
| chr19:53923104
|
TC | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+7600delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923104 | ||||||
| chr19:53923113
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7608G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923113 | ||||||
| chr19:53923113
|
GAGTTGCC others(530): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7641_424+8177d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923113 | |||||
| chr19:53923115
|
G | GT | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7612dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923115 | |||||
| chr19:53923118
|
G | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7613G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923118 | ||||||
| chr19:53923119
|
C | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7614C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923119 | ||||||
| chr19:53923125
|
GT | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7621delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923125 | ||||||
| chr19:53923126
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0245a0001c0001t0001g0335others(1): Show | 4 | HG01496.hp2 HG01891.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7621T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923126 | ||||||
| chr19:53923131
|
TC | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0061others(33): Show | 37 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+7627delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923131 | ||||||
| chr19:53923145
|
G | GT | 35 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(32): Show | 36 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.424+7640_424+7641i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923145 | ||||||
| chr19:53923146
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(12): Show | 16 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7641C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923146 | ||||||
| chr19:53923149
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7644C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923149 | ||||||
| chr19:53923153
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0072others(30): Show | 34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7648T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923153 | ||||||
| chr19:53923168
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+7663A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923168 | ||||||
| chr19:53923172
|
G | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7667G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923172 | ||||||
| chr19:53923173
|
T | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0087others(59): Show | 65 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.424+7668T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923173 | ||||||
| chr19:53923173
|
T | TC | 9 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+7671dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923173 | |||||
| chr19:53923173
|
TCCCAGGT others(46): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7690_424+7742d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923173 | |||||
| chr19:53923175
|
C | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.424+7670C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923175 | ||||||
| chr19:53923179
|
GTCTGGTC others(290): Show |
G | 7 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7675_424+7971d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923179 | ||||||
| chr19:53923180
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0072 | 3 | HG01109.hp2 HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7675T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923180 | ||||||
| chr19:53923183
|
GGTCATTG others(19): Show |
G | 1 | a0001c0001t0002g0321 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+7690_424+7715d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923183 | |||||
| chr19:53923185
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7681delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923185 | ||||||
| chr19:53923185
|
TCATTGGT others(154): Show |
T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7681_424+7841d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923185 | ||||||
| chr19:53923195
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 121 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.424+7690G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923195 | ||||||
| chr19:53923200
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0003g0026 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+7695T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923200 | ||||||
| chr19:53923206
|
G | GT | 8 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7701_424+7702i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923206 | ||||||
| chr19:53923209
|
C | G | 114 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.424+7704C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923209 | ||||||
| chr19:53923220
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7715G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923220 | ||||||
| chr19:53923226
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0010g0233a0001c0001t0015g0031 | 3 | HG03669.hp2 HG03834.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+7721C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923226 | ||||||
| chr19:53923232
|
GTCTGGTC others(210): Show |
G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7728_424+7944d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923232 | ||||||
| chr19:53923233
|
TCTGGTCA others(262): Show |
T | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+7748_424+8016d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923233 | |||||
| chr19:53923238
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7734delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923238 | ||||||
| chr19:53923243
|
G | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0194others(41): Show | 45 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7738G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923243 | ||||||
| chr19:53923247
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0003g0026 | 2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7742G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923247 | ||||||
| chr19:53923252
|
GTCCCAGG others(182): Show |
G | 1 | a0001c0001t0002g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+7748_424+7936d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923252 | ||||||
| chr19:53923253
|
T | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0172others(31): Show | 35 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.424+7748T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923253 | ||||||
| chr19:53923253
|
T | TC | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7751dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923253 | |||||
| chr19:53923260
|
T | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7755T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923260 | ||||||
| chr19:53923274
|
C | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0032others(36): Show | 40 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.424+7769C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923274 | ||||||
| chr19:53923274
|
CAGTTGCC others(315): Show |
C | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7802_424+8123d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923274 | |||||
| chr19:53923279
|
G | GT | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7774_424+7775i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923279 | ||||||
| chr19:53923280
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7775C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923280 | ||||||
| chr19:53923280
|
C | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0246others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7775C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923280 | ||||||
| chr19:53923280
|
CCCCAGGT others(262): Show |
C | 55 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0093others(52): Show | 58 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.424+7802_424+8070d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923280 | |||||
| chr19:53923282
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0003g0026 | 2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7777C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923282 | ||||||
| chr19:53923287
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7782T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923287 | ||||||
| chr19:53923294
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7789A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923294 | ||||||
| chr19:53923301
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7796G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923301 | ||||||
| chr19:53923306
|
G | GT | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7801_424+7802i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923306 | ||||||
| chr19:53923306
|
GACTCAGG others(101): Show |
G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7802_424+7909d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923306 | ||||||
| chr19:53923307
|
A | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0061others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7802A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923307 | ||||||
| chr19:53923307
|
A | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0209others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7802A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923307 | ||||||
| chr19:53923309
|
T | C | 40 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0032others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.424+7804T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923309 | ||||||
| chr19:53923310
|
C | T | 1 | a0001c0001t0020g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.424+7805C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923310 | ||||||
| chr19:53923313
|
G | GC | 7 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7809dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923313 | |||||
| chr19:53923313
|
G | GTCTGGTC others(47): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7808_424+7809i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923313 | ||||||
| chr19:53923320
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7815A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923320 | ||||||
| chr19:53923332
|
GCCCCAGG others(102): Show |
G | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+7855_424+7963d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923332 | |||||
| chr19:53923333
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7828C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923333 | ||||||
| chr19:53923338
|
GGCCTGGT others(155): Show |
G | 3 | a0001c0001t0001g0209a0001c0001t0001g0238a0001c0001t0001g0256 | 3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7835_424+7996d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923338 | |||||
| chr19:53923340
|
C | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0061others(29): Show | 33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+7835C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923340 | ||||||
| chr19:53923360
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0065others(40): Show | 44 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+7855C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923360 | ||||||
| chr19:53923366
|
GT | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7862delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923366 | ||||||
| chr19:53923366
|
GTCTGGTC others(290): Show |
G | 1 | a0001c0001t0020g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.424+7862_424+8158d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923366 | ||||||
| chr19:53923367
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+7862T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923367 | ||||||
| chr19:53923370
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+7865G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923370 | ||||||
| chr19:53923372
|
TC | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0245others(2): Show | 5 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7868delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923372 | ||||||
| chr19:53923373
|
C | CATTGGTG others(20): Show |
10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7917_424+7943d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923373 | |||||
| chr19:53923386
|
G | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7881G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923386 | ||||||
| chr19:53923386
|
GT | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+7882delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923386 | ||||||
| chr19:53923387
|
TC | T | 28 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0192others(25): Show | 29 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+7886delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923387 | |||||
| chr19:53923387
|
TCCCCAGG others(48): Show |
T | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7886_424+7940d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923387 | |||||
| chr19:53923400
|
T | TC | 42 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(39): Show | 44 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+7895_424+7896i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923400 | ||||||
| chr19:53923408
|
G | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0246others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7903G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923408 | ||||||
| chr19:53923413
|
G | GTCCCCAG others(20): Show |
3 | a0001c0001t0001g0212a0001c0001t0002g0316a0001c0001t0010g0233 | 3 | HG02818.hp1 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+7934_424+7935i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923413 | |||||
| chr19:53923413
|
G | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0019g0281 | 3 | HG01891.hp1 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+7908G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923413 | ||||||
| chr19:53923413
|
GT | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0192others(25): Show | 29 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+7909delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923413 | ||||||
| chr19:53923415
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7910C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923415 | ||||||
| chr19:53923416
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7911C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923416 | ||||||
| chr19:53923422
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00597.hp1 HG01496.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7917T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923422 | ||||||
| chr19:53923427
|
T | TC | 40 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 41 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.424+7922_424+7923i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923427 | ||||||
| chr19:53923434
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7929G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923434 | ||||||
| chr19:53923438
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7933T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923438 | ||||||
| chr19:53923440
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7935G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923440 | ||||||
| chr19:53923441
|
TC | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0172others(28): Show | 32 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+7940delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923441 | |||||
| chr19:53923445
|
C | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0246others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7940C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923445 | ||||||
| chr19:53923448
|
GC | G | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7945delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923448 | |||||
| chr19:53923449
|
C | A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7944C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923449 | ||||||
| chr19:53923449
|
C | CCTGGTAT others(20): Show |
1 | a0001c0001t0005g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+7949_424+7950i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923449 | |||||
| chr19:53923449
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7944C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923449 | ||||||
| chr19:53923454
|
TC | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+7950delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923454 | ||||||
| chr19:53923454
|
TCATTGGT others(451): Show |
T | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7950_424+8407d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923454 | ||||||
| chr19:53923456
|
A | G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7951A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923456 | ||||||
| chr19:53923463
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0192 | 2 | HG01891.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.424+7958G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923463 | ||||||
| chr19:53923469
|
T | C | 17 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(14): Show | 17 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+7964T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923469 | ||||||
| chr19:53923469
|
T | TC | 43 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(40): Show | 45 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7967dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923469 | |||||
| chr19:53923469
|
TCCCAGGT others(45): Show |
T | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+7968_424+8019d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923469 | |||||
| chr19:53923474
|
G | C | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7969G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923474 | ||||||
| chr19:53923476
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(40): Show | 45 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7971T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923476 | ||||||
| chr19:53923492
|
G | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0292others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7987G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923492 | ||||||
| chr19:53923493
|
T | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7988T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923493 | ||||||
| chr19:53923496
|
T | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 16 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+7991T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923496 | ||||||
| chr19:53923502
|
G | GA | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7997_424+7998i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | ||||||
| chr19:53923502
|
G | GCCTGGTC others(77): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7998_424+7999i others(86): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923502 | |||||
| chr19:53923502
|
G | GCTGGTCA others(20): Show |
2 | a0001c0001t0001g0212a0001c0001t0010g0233 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8017_424+8043d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923502 | |||||
| chr19:53923502
|
G | GT | 15 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7997_424+7998i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | ||||||
| chr19:53923502
|
G | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0238a0001c0001t0001g0256 | 3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7997G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | ||||||
| chr19:53923512
|
G | A | 9 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG00323.hp1 HG02486.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8007G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923512 | ||||||
| chr19:53923516
|
G | C | 11 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8011G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923516 | ||||||
| chr19:53923518
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8013G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923518 | ||||||
| chr19:53923520
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0292others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+8015T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923520 | ||||||
| chr19:53923521
|
G | GT | 10 | a0001c0001t0001g0032a0001c0001t0001g0103a0001c0001t0001g0115others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8016_424+8017i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923521 | ||||||
| chr19:53923522
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp1 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+8017C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923522 | ||||||
| chr19:53923528
|
GT | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(4): Show | 8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8024delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923528 | ||||||
| chr19:53923529
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0192a0001c0001t0001g0355 | 3 | HG01891.hp1 HG03209.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.424+8024T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923529 | ||||||
| chr19:53923529
|
TCTGGTCA others(154): Show |
T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8071_424+8231d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923529 | |||||
| chr19:53923536
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8031A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923536 | ||||||
| chr19:53923543
|
G | C | 10 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0230others(7): Show | 10 | HG00323.hp1 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8038G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923543 | ||||||
| chr19:53923546
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+8041T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923546 | ||||||
| chr19:53923549
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+8044T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923549 | ||||||
| chr19:53923552
|
C | T | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+8047C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923552 | ||||||
| chr19:53923555
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8051delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923555 | ||||||
| chr19:53923556
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+8051T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923556 | ||||||
| chr19:53923556
|
T | C | 13 | a0001c0001t0001g0032a0001c0001t0001g0192a0001c0001t0001g0196others(10): Show | 13 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+8051T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923556 | ||||||
| chr19:53923561
|
T | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8056T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923561 | ||||||
| chr19:53923562
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8057C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923562 | ||||||
| chr19:53923563
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8058A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923563 | ||||||
| chr19:53923564
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8059T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923564 | ||||||
| chr19:53923569
|
G | A | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+8064G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923569 | ||||||
| chr19:53923570
|
G | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0245a0001c0001t0001g0328others(2): Show | 5 | HG01496.hp2 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8065G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923570 | ||||||
| chr19:53923570
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8065G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923570 | ||||||
| chr19:53923572
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8067G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923572 | ||||||
| chr19:53923576
|
T | C | 14 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0131others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+8071T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923576 | ||||||
| chr19:53923576
|
T | TC | 11 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(8): Show | 11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8074dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | |||||
| chr19:53923576
|
TCCCAGGC others(18): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+8075_424+8099d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | |||||
| chr19:53923576
|
TCCCAGGC others(154): Show |
T | 27 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0246others(24): Show | 28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+8078_424+8238d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | |||||
| chr19:53923579
|
C | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0093others(62): Show | 68 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+8074C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923579 | ||||||
| chr19:53923582
|
G | GC | 76 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0093others(73): Show | 79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8078dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923582 | |||||
| chr19:53923582
|
G | GT | 20 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(17): Show | 21 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+8077_424+8078i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | ||||||
| chr19:53923582
|
G | GTCTGGTC others(76): Show |
1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8077_424+8078i others(85): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | ||||||
| chr19:53923582
|
G | GTCTGGTC others(47): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+8077_424+8078i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | ||||||
| chr19:53923596
|
G | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0131 | 3 | HG01109.hp2 HG03579.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8091G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923596 | ||||||
| chr19:53923598
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8093G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923598 | ||||||
| chr19:53923601
|
G | GT | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(79): Show | 86 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.424+8096_424+8097i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923601 | ||||||
| chr19:53923602
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0200others(6): Show | 9 | HG01496.hp2 HG01891.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8097C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923602 | ||||||
| chr19:53923605
|
C | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0328a0001c0001t0001g0335others(1): Show | 4 | HG01496.hp2 HG02280.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8100C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923605 | ||||||
| chr19:53923608
|
GT | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0015g0031 | 3 | HG01891.hp1 NA18950.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+8104delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923608 | ||||||
| chr19:53923609
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(85): Show | 92 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.424+8104T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923609 | ||||||
| chr19:53923614
|
TC | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8110delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923614 | ||||||
| chr19:53923615
|
CATTGGTG others(73): Show |
C | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+8111_424+8190d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923615 | ||||||
| chr19:53923619
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0010g0233 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8114G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923619 | ||||||
| chr19:53923623
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8118G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923623 | ||||||
| chr19:53923629
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(15): Show | 19 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.424+8124T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923629 | ||||||
| chr19:53923629
|
T | TC | 5 | a0001c0001t0001g0200a0001c0001t0001g0245a0001c0001t0001g0328others(2): Show | 5 | HG01496.hp2 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8127dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923629 | |||||
| chr19:53923632
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8127C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923632 | ||||||
| chr19:53923635
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8130G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | ||||||
| chr19:53923635
|
GT | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0093others(62): Show | 68 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+8131delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | ||||||
| chr19:53923635
|
GTCTGGTC others(21): Show |
G | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(7): Show | 10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8131_424+8158d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | ||||||
| chr19:53923636
|
T | C | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG01496.hp2 HG02135.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8131T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923636 | ||||||
| chr19:53923650
|
C | CAGTTGCC others(101): Show |
2 | a0001c0001t0001g0212a0001c0001t0010g0233 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8180_424+8181i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923650 | |||||
| chr19:53923650
|
C | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(90): Show | 97 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.424+8145C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923650 | ||||||
| chr19:53923650
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8145C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923650 | ||||||
| chr19:53923652
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8147G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923652 | ||||||
| chr19:53923655
|
G | GT | 7 | a0001c0001t0001g0032a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8150_424+8151i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923655 | ||||||
| chr19:53923656
|
C | T | 7 | a0001c0001t0001g0245a0001c0001t0001g0328a0001c0001t0001g0335others(4): Show | 7 | HG01496.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8151C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923656 | ||||||
| chr19:53923657
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8152C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923657 | ||||||
| chr19:53923662
|
GT | G | 4 | a0001c0001t0001g0245a0001c0001t0001g0328a0001c0001t0001g0335others(1): Show | 4 | HG01496.hp2 HG02280.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8158delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923662 | ||||||
| chr19:53923663
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG00609.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8158T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923663 | ||||||
| chr19:53923676
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8171G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923676 | ||||||
| chr19:53923677
|
G | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8172G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923677 | ||||||
| chr19:53923683
|
T | C | 22 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(19): Show | 22 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+8178T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923683 | ||||||
| chr19:53923683
|
T | TCCTAGGC others(74): Show |
1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+8180_424+8181i others(83): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923683 | |||||
| chr19:53923686
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8181C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923686 | ||||||
| chr19:53923689
|
GC | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02135.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8186delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923689 | |||||
| chr19:53923690
|
C | CCTGGTCA others(47): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8200_424+8201i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923690 | |||||
| chr19:53923690
|
C | CCTGGTCA others(102): Show |
2 | a0001c0001t0001g0051a0001c0001t0016g0052 | 2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424+8208_424+8209i others(111): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923690 | |||||
| chr19:53923690
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(96): Show | 103 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.424+8185C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923690 | ||||||
| chr19:53923695
|
TCATTGGT others(48): Show |
T | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8191_424+8245d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923695 | ||||||
| chr19:53923705
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8200A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923705 | ||||||
| chr19:53923706
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8201G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923706 | ||||||
| chr19:53923710
|
T | C | 13 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(10): Show | 13 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+8205T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923710 | ||||||
| chr19:53923710
|
T | TCCCCAGG others(75): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 9 | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8208_424+8209i others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923710 | |||||
| chr19:53923717
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0254a0001c0001t0019g0281 | 3 | HG01952.hp2 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8212T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923717 | ||||||
| chr19:53923720
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8215G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923720 | ||||||
| chr19:53923733
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8228G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923733 | ||||||
| chr19:53923735
|
T | TG | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8231dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923735 | |||||
| chr19:53923737
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(32): Show | 37 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+8232C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923737 | ||||||
| chr19:53923743
|
GT | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 11 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+8239delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923743 | ||||||
| chr19:53923754
|
G | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0006g0351others(1): Show | 4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8249G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923754 | ||||||
| chr19:53923758
|
G | C | 2 | a0001c0001t0015g0031a0001c0001t0020g0058 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+8253G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923758 | ||||||
| chr19:53923764
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8259C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923764 | ||||||
| chr19:53923771
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8266T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923771 | ||||||
| chr19:53923779
|
T | C | 3 | a0001c0001t0004g0054a0001c0001t0004g0056a0001c0001t0005g0055 | 3 | HG02055.hp2 HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424+8274T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923779 | ||||||
| chr19:53923785
|
C | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0048others(46): Show | 51 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.424+8280C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923785 | ||||||
| chr19:53923787
|
G | C | 3 | a0001c0001t0001g0059a0001c0001t0003g0026a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8282G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923787 | ||||||
| chr19:53923791
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8286C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923791 | ||||||
| chr19:53923793
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8288C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923793 | ||||||
| chr19:53923812
|
G | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0049others(40): Show | 45 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+8307G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923812 | ||||||
| chr19:53923817
|
G | GT | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8312_424+8313i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923817 | ||||||
| chr19:53923818
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8313C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923818 | ||||||
| chr19:53923818
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0355 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8313C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923818 | ||||||
| chr19:53923820
|
C | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0062others(73): Show | 79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8315C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923820 | ||||||
| chr19:53923824
|
GT | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0062others(73): Show | 79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8320delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923824 | ||||||
| chr19:53923825
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 29 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.424+8320T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923825 | ||||||
| chr19:53923825
|
T | TCTGGTCA others(20): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 9 | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8374_424+8400d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923825 | |||||
| chr19:53923825
|
TCTGGTCA others(20): Show |
T | 2 | a0001c0001t0001g0119a0001c0001t0001g0132 | 2 | NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+8374_424+8400d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923825 | |||||
| chr19:53923839
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8334G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923839 | ||||||
| chr19:53923841
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8336G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923841 | ||||||
| chr19:53923844
|
G | GT | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8339_424+8340i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923844 | ||||||
| chr19:53923845
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8340C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923845 | ||||||
| chr19:53923852
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8347C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923852 | ||||||
| chr19:53923853
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8348C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923853 | ||||||
| chr19:53923866
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8361G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923866 | ||||||
| chr19:53923872
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0355 | 2 | HG03209.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8367C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923872 | ||||||
| chr19:53923874
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8369C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923874 | ||||||
| chr19:53923878
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8373G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923878 | ||||||
| chr19:53923879
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+8374C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923879 | ||||||
| chr19:53923893
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8388G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923893 | ||||||
| chr19:53923895
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8390G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923895 | ||||||
| chr19:53923899
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0003g0026 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8394C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923899 | ||||||
| chr19:53923901
|
C | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8396C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923901 | ||||||
| chr19:53923906
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8401T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923906 | ||||||
| chr19:53923920
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0355 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8415G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923920 | ||||||
| chr19:53923925
|
GT | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0355others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8421delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923925 | ||||||
| chr19:53923925
|
GTCCCCAG others(131): Show |
G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8421_424+8558d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923925 | ||||||
| chr19:53923930
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8425C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923930 | ||||||
| chr19:53923934
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8429T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923934 | ||||||
| chr19:53923934
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+8429T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923934 | ||||||
| chr19:53923939
|
T | TC | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0032others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+8434_424+8435i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923939 | ||||||
| chr19:53923947
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8442G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923947 | ||||||
| chr19:53923949
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8444G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923949 | ||||||
| chr19:53923961
|
T | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8456T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923961 | ||||||
| chr19:53923965
|
G | A | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8460G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923965 | ||||||
| chr19:53923966
|
T | TC | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8461_424+8462i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923966 | ||||||
| chr19:53923974
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8469G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923974 | ||||||
| chr19:53923979
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8475delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923979 | ||||||
| chr19:53923980
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8475T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923980 | ||||||
| chr19:53923981
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8476C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923981 | ||||||
| chr19:53923988
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8483C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923988 | ||||||
| chr19:53923993
|
TC | T | 3 | a0001c0001t0001g0059a0001c0001t0003g0026a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8489delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923993 | ||||||
| chr19:53924002
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8497G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924002 | ||||||
| chr19:53924008
|
TC | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8507delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924008 | |||||
| chr19:53924009
|
C | CCGAGGTC others(225): Show |
1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8505_424+8506i others(234): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924009 | |||||
| chr19:53924012
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8507C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924012 | ||||||
| chr19:53924016
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8511C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924016 | ||||||
| chr19:53924016
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8511C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924016 | ||||||
| chr19:53924030
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0355 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8525G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924030 | ||||||
| chr19:53924032
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8527G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924032 | ||||||
| chr19:53924036
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8531C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924036 | ||||||
| chr19:53924039
|
C | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8534C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924039 | ||||||
| chr19:53924043
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8538C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924043 | ||||||
| chr19:53924048
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8544delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924048 | ||||||
| chr19:53924062
|
GT | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0131others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8558delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924062 | ||||||
| chr19:53924071
|
T | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8566T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924071 | ||||||
| chr19:53924077
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8572C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924077 | ||||||
| chr19:53924085
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8580G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924085 | ||||||
| chr19:53924087
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0003g0026 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+8582G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924087 | ||||||
| chr19:53924090
|
GT | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+8586delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924090 | ||||||
| chr19:53924099
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8594T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924099 | ||||||
| chr19:53924101
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8596T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924101 | ||||||
| chr19:53924101
|
TG | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8599delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924101 | |||||
| chr19:53924104
|
G | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8599G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924104 | ||||||
| chr19:53924105
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8600T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924105 | ||||||
| chr19:53924113
|
G | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8608G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924113 | ||||||
| chr19:53924115
|
C | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8610C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924115 | ||||||
| chr19:53924118
|
GCCCCAGG others(19): Show |
G | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8614_424+8639d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924118 | ||||||
| chr19:53924118
|
GCCCCAGG others(156): Show |
G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+8627_424+8789d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924118 | |||||
| chr19:53924119
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8614C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924119 | ||||||
| chr19:53924122
|
C | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8617C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924122 | ||||||
| chr19:53924126
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8621T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924126 | ||||||
| chr19:53924128
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8623T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924128 | ||||||
| chr19:53924130
|
GT | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8627delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924130 | |||||
| chr19:53924132
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.424+8627T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924132 | ||||||
| chr19:53924141
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8636A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924141 | ||||||
| chr19:53924142
|
C | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8637C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924142 | ||||||
| chr19:53924143
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8638T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924143 | ||||||
| chr19:53924146
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0019g0281 | 3 | HG02109.hp1 HG03098.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8641C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924146 | ||||||
| chr19:53924148
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8643C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924148 | ||||||
| chr19:53924152
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8648delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924152 | ||||||
| chr19:53924156
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8651G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924156 | ||||||
| chr19:53924167
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8662G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924167 | ||||||
| chr19:53924171
|
TG | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0003g0026others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8668delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924171 | |||||
| chr19:53924172
|
GGT | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8668_424+8669d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924172 | ||||||
| chr19:53924173
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8668G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924173 | ||||||
| chr19:53924174
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0131 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8669T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924174 | ||||||
| chr19:53924180
|
GT | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8676delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924180 | ||||||
| chr19:53924187
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8682C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924187 | ||||||
| chr19:53924195
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8690G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924195 | ||||||
| chr19:53924195
|
G | T | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+8690G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924195 | ||||||
| chr19:53924196
|
A | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8691A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924196 | ||||||
| chr19:53924197
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8692G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924197 | ||||||
| chr19:53924201
|
T | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8696T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924201 | ||||||
| chr19:53924204
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8699C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924204 | ||||||
| chr19:53924207
|
GT | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8703delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924207 | ||||||
| chr19:53924208
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8703T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924208 | ||||||
| chr19:53924211
|
G | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0114a0001c0001t0001g0173 | 3 | HG02074.hp2 HG04184.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.424+8706G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924211 | ||||||
| chr19:53924222
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0061others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8717C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924222 | ||||||
| chr19:53924228
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8723C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924228 | ||||||
| chr19:53924231
|
C | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8726C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924231 | ||||||
| chr19:53924240
|
TC | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8736delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924240 | ||||||
| chr19:53924249
|
G | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8744G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924249 | ||||||
| chr19:53924251
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8746G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924251 | ||||||
| chr19:53924255
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8750C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924255 | ||||||
| chr19:53924255
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8750C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924255 | ||||||
| chr19:53924257
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8752C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924257 | ||||||
| chr19:53924261
|
G | T | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8756G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924261 | ||||||
| chr19:53924267
|
TC | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8763delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924267 | ||||||
| chr19:53924278
|
C | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG00597.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+8773C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924278 | ||||||
| chr19:53924281
|
T | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.424+8776T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924281 | ||||||
| chr19:53924282
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8777C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924282 | ||||||
| chr19:53924284
|
C | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+8779C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924284 | ||||||
| chr19:53924285
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8780C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924285 | ||||||
| chr19:53924288
|
G | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8783G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924288 | ||||||
| chr19:53924289
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0019g0281 | 3 | HG02109.hp1 HG03098.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8784T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924289 | ||||||
| chr19:53924294
|
TC | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8790delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924294 | ||||||
| chr19:53924305
|
G | C | 3 | a0001c0001t0001g0059a0001c0001t0003g0026a0001c0001t0019g0281 | 3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8800G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924305 | ||||||
| chr19:53924305
|
G | GTTGCCCC others(20): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+8806_424+8832d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924305 | |||||
| chr19:53924312
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8807C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924312 | ||||||
| chr19:53924316
|
C | G | 2 | a0001c0001t0001g0326a0001c0001t0003g0026 | 2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.424+8811C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924316 | ||||||
| chr19:53924316
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+8811C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924316 | ||||||
| chr19:53924322
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8817C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924322 | ||||||
| chr19:53924332
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0131 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8827C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924332 | ||||||
| chr19:53924337
|
CG | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8833delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924337 | ||||||
| chr19:53924338
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8833G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924338 | ||||||
| chr19:53924339
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924339 | ||||||
| chr19:53924343
|
T | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8838T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924343 | ||||||
| chr19:53924359
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8854G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924359 | ||||||
| chr19:53924362
|
GTC | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8858_424+8859d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924362 | ||||||
| chr19:53924363
|
TCCCCAGG others(680): Show |
T | 2 | a0001c0001t0001g0119a0001c0001t0001g0132 | 2 | NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+8886_424+9572d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924363 | |||||
| chr19:53924367
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8862C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924367 | ||||||
| chr19:53924367
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8862C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924367 | ||||||
| chr19:53924371
|
T | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8866T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924371 | ||||||
| chr19:53924387
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8882G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924387 | ||||||
| chr19:53924390
|
GT | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8886delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924390 | ||||||
| chr19:53924399
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8894C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924399 | ||||||
| chr19:53924411
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8906T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924411 | ||||||
| chr19:53924413
|
G | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8908G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924413 | ||||||
| chr19:53924415
|
G | C | 3 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG02647.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8910G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924415 | ||||||
| chr19:53924419
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8914C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924419 | ||||||
| chr19:53924442
|
G | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8937G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924442 | ||||||
| chr19:53924443
|
T | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8938T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924443 | ||||||
| chr19:53924446
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(5): Show | 8 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8941T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924446 | ||||||
| chr19:53924446
|
T | TCCCAGGC others(153): Show |
1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8947_424+8948i others(162): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924446 | |||||
| chr19:53924452
|
GT | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8948delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924452 | ||||||
| chr19:53924467
|
G | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8962G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924467 | ||||||
| chr19:53924469
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8964G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924469 | ||||||
| chr19:53924473
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8968T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924473 | ||||||
| chr19:53924473
|
TCCGAGGT others(150): Show |
T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8971_424+9127d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924473 | |||||
| chr19:53924476
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.424+8971G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924476 | ||||||
| chr19:53924476
|
G | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8971G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924476 | ||||||
| chr19:53924480
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8975T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924480 | ||||||
| chr19:53924485
|
T | TC | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8980_424+8981i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924485 | ||||||
| chr19:53924498
|
GT | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8994delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924498 | ||||||
| chr19:53924507
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9002C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924507 | ||||||
| chr19:53924513
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9008T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924513 | ||||||
| chr19:53924523
|
G | C | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+9018G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924523 | ||||||
| chr19:53924527
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9022C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924527 | ||||||
| chr19:53924533
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9028G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924533 | ||||||
| chr19:53924533
|
GT | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9029delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924533 | ||||||
| chr19:53924539
|
T | TG | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9034_424+9035i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924539 | ||||||
| chr19:53924548
|
A | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9043A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924548 | ||||||
| chr19:53924553
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9048T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924553 | ||||||
| chr19:53924556
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9051G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924556 | ||||||
| chr19:53924565
|
T | TCATTGGT others(46): Show |
1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9060_424+9061i others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924565 | ||||||
| chr19:53924573
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9068G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924573 | ||||||
| chr19:53924585
|
G | GT | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+9080_424+9081i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924585 | ||||||
| chr19:53924590
|
TC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9086delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924590 | ||||||
| chr19:53924601
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9096G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924601 | ||||||
| chr19:53924604
|
G | GTCCCAGG others(152): Show |
1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+9099_424+9100i others(161): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924604 | ||||||
| chr19:53924607
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9102C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924607 | ||||||
| chr19:53924608
|
A | AG | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9105dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924608 | |||||
| chr19:53924610
|
G | GT | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9105_424+9106i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924610 | ||||||
| chr19:53924616
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9111C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924616 | ||||||
| chr19:53924626
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9121C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924626 | ||||||
| chr19:53924636
|
GCTGGTCA others(71): Show |
G | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9132_424+9209d others(80): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924636 | ||||||
| chr19:53924639
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+9134G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924639 | ||||||
| chr19:53924642
|
C | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9137C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924642 | ||||||
| chr19:53924650
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9145G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924650 | ||||||
| chr19:53924651
|
A | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9146A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924651 | ||||||
| chr19:53924652
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0003g0026 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+9147G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924652 | ||||||
| chr19:53924656
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9151T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924656 | ||||||
| chr19:53924659
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9154G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924659 | ||||||
| chr19:53924668
|
T | TC | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0026 | 3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9163_424+9164i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924668 | ||||||
| chr19:53924674
|
T | G | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+9169T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924674 | ||||||
| chr19:53924682
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9177C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924682 | ||||||
| chr19:53924703
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9198A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924703 | ||||||
| chr19:53924708
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9203C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924708 | ||||||
| chr19:53924711
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9206C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924711 | ||||||
| chr19:53924714
|
T | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0135others(2): Show | 5 | HG01891.hp1 HG02922.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+9209T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924714 | ||||||
| chr19:53924720
|
T | TC | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9215_424+9216i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924720 | ||||||
| chr19:53924741
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9236T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924741 | ||||||
| chr19:53924742
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9237C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924742 | ||||||
| chr19:53924757
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9252C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924757 | ||||||
| chr19:53924763
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9258T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924763 | ||||||
| chr19:53924766
|
GGCTGGTC others(19): Show |
G | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9284_424+9309d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924766 | |||||
| chr19:53924767
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9262G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924767 | ||||||
| chr19:53924783
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9278C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924783 | ||||||
| chr19:53924789
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0131 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9284T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924789 | ||||||
| chr19:53924792
|
T | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.424+9287T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924792 | ||||||
| chr19:53924793
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9288G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924793 | ||||||
| chr19:53924793
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9288G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924793 | ||||||
| chr19:53924800
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9295A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924800 | ||||||
| chr19:53924809
|
C | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9304C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924809 | ||||||
| chr19:53924833
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+9328G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924833 | ||||||
| chr19:53924836
|
G | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0093others(49): Show | 53 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+9331G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924836 | ||||||
| chr19:53924843
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9338C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924843 | ||||||
| chr19:53924847
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9342T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924847 | ||||||
| chr19:53924852
|
T | G | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9347T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924852 | ||||||
| chr19:53924853
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9348C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924853 | ||||||
| chr19:53924863
|
C | G | 56 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0093others(53): Show | 57 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.424+9358C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924863 | ||||||
| chr19:53924869
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9364C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924869 | ||||||
| chr19:53924870
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9365C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924870 | ||||||
| chr19:53924871
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9366A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924871 | ||||||
| chr19:53924879
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9374C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924879 | ||||||
| chr19:53924885
|
T | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9380T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924885 | ||||||
| chr19:53924887
|
T | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0003g0028others(1): Show | 4 | HG01891.hp1 HG02922.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9382T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924887 | ||||||
| chr19:53924889
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9384C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924889 | ||||||
| chr19:53924917
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9412T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924917 | ||||||
| chr19:53924920
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9415C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924920 | ||||||
| chr19:53924943
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9438G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924943 | ||||||
| chr19:53924944
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9439T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924944 | ||||||
| chr19:53924947
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0271 | 2 | HG01891.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.424+9442T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924947 | ||||||
| chr19:53924947
|
TCCCAGGC others(283): Show |
T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9449_424+9738d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924947 | |||||
| chr19:53924959
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0271 | 3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9454G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924959 | ||||||
| chr19:53924961
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.424+9456T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924961 | ||||||
| chr19:53924963
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9458G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924963 | ||||||
| chr19:53924966
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9461G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924966 | ||||||
| chr19:53924967
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9462G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924967 | ||||||
| chr19:53924967
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9462G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924967 | ||||||
| chr19:53924968
|
T | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0271 | 3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9463T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924968 | ||||||
| chr19:53924969
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9464G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924969 | ||||||
| chr19:53924973
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0131 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9468T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924973 | ||||||
| chr19:53924976
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924976 | ||||||
| chr19:53924976
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0271 | 3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9471G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924976 | ||||||
| chr19:53924988
|
T | G | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9483T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924988 | ||||||
| chr19:53924994
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9489A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924994 | ||||||
| chr19:53924999
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9494C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924999 | ||||||
| chr19:53925002
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9497C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925002 | ||||||
| chr19:53925011
|
T | TCATTGGT others(48): Show |
1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9506_424+9507i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925011 | ||||||
| chr19:53925011
|
TATTGGTG others(19): Show |
T | 1 | a0001c0001t0001g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9522_424+9547d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | |||||
| chr19:53925011
|
TATTGGTG others(46): Show |
T | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+9516_424+9568d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | |||||
| chr19:53925011
|
TATTGGTG others(73): Show |
T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9548_424+9627d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | |||||
| chr19:53925021
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0222 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+9516C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925021 | ||||||
| chr19:53925025
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9520C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925025 | ||||||
| chr19:53925025
|
CCTAGGGC others(72): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+9522_424+9600d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925025 | |||||
| chr19:53925027
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0131 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9522T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925027 | ||||||
| chr19:53925028
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9523A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925028 | ||||||
| chr19:53925029
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9524G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925029 | ||||||
| chr19:53925031
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9526G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925031 | ||||||
| chr19:53925037
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9532C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925037 | ||||||
| chr19:53925046
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9541A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925046 | ||||||
| chr19:53925047
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0271 | 3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9542C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925047 | ||||||
| chr19:53925051
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9546C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925051 | ||||||
| chr19:53925054
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9549C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925054 | ||||||
| chr19:53925085
|
TCTGGTCA others(19): Show |
T | 6 | a0001c0001t0001g0126a0001c0001t0001g0171a0001c0001t0001g0279others(3): Show | 6 | HG01168.hp2 HG01261.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9628_424+9653d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925085 | |||||
| chr19:53925090
|
TC | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9586delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925090 | ||||||
| chr19:53925101
|
C | G | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+9596C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925101 | ||||||
| chr19:53925104
|
G | GC | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+9601dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925104 | |||||
| chr19:53925107
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9602T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925107 | ||||||
| chr19:53925111
|
G | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9606G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925111 | ||||||
| chr19:53925153
|
CTTGCCCC others(20): Show |
C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9673_424+9699d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925153 | |||||
| chr19:53925167
|
G | GGTCATTG others(23): Show |
1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9663_424+9692d others(32): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925167 | |||||
| chr19:53925178
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(143): Show | 151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.424+9673A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925178 | ||||||
| chr19:53925181
|
T | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9676T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925181 | ||||||
| chr19:53925217
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9712G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925217 | ||||||
| chr19:53925229
|
C | T | 4 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0005g0348others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9724C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925229 | ||||||
| chr19:53925230
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+9725G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925230 | ||||||
| chr19:53925256
|
TG | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0026a0001c0001t0003g0027 | 4 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9753delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925256 | |||||
| chr19:53925271
|
T | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9766T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925271 | ||||||
| chr19:53925275
|
G | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+9770G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925275 | ||||||
| chr19:53925291
|
T | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9786T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925291 | ||||||
| chr19:53925326
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9821C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925326 | ||||||
| chr19:53925336
|
G | A | 1 | a0001c0001t0013g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+9831G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925336 | ||||||
| chr19:53925372
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9867C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925372 | ||||||
| chr19:53925394
|
G | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9889G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925394 | ||||||
| chr19:53925400
|
C | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9895C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925400 | ||||||
| chr19:53925406
|
C | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9901C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925406 | ||||||
| chr19:53925410
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+9905T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925410 | ||||||
| chr19:53925425
|
T | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9920T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925425 | ||||||
| chr19:53925451
|
C | A | 1 | a0001c0001t0013g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+9946C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925451 | ||||||
| chr19:53925453
|
A | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9948A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925453 | ||||||
| chr19:53925454
|
C | G | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+9949C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925454 | ||||||
| chr19:53925459
|
A | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9954A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925459 | ||||||
| chr19:53925463
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9958C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925463 | ||||||
| chr19:53925474
|
G | C | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9969G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925474 | ||||||
| chr19:53925484
|
G | GCTGGTCA others(20): Show |
120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+10005_424+1000 others(31): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925484 | |||||
| chr19:53925484
|
G | GCTGGTCA others(20): Show |
4 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0006g0351others(1): Show | 4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9994_424+9995i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925484 | |||||
| chr19:53925500
|
C | G | 4 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0003g0028others(1): Show | 4 | HG02080.hp2 HG02135.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9995C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925500 | ||||||
| chr19:53925502
|
T | TGCCCCAG others(20): Show |
1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+10005_424+1000 others(31): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925502 | |||||
| chr19:53925504
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9999C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925504 | ||||||
| chr19:53925526
|
G | C | 4 | a0001c0001t0001g0215a0001c0001t0001g0234a0001c0001t0003g0028others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10021G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925526 | ||||||
| chr19:53925530
|
T | C | 4 | a0001c0001t0001g0215a0001c0001t0001g0234a0001c0001t0003g0028others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10025T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925530 | ||||||
| chr19:53925536
|
G | GCTGGTCA others(46): Show |
2 | a0001c0001t0001g0215a0001c0001t0001g0234 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.424+10046_424+1004 others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925536 | |||||
| chr19:53925562
|
GT | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0234a0001c0001t0003g0028others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10058delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925562 | ||||||
| chr19:53925563
|
T | TCTGGTCA others(19): Show |
152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 158 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.424+10070_424+1009 others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925563 | |||||
| chr19:53925583
|
C | CCCCAGGC others(18): Show |
1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+10095_424+1009 others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925583 | |||||
| chr19:53925599
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.424+10094G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925599 | ||||||
| chr19:53925614
|
G | A | 5 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0199others(2): Show | 5 | HG02027.hp1 HG02083.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10109G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925614 | ||||||
| chr19:53925616
|
T | C | 1 | a0001c0001t0005g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.424+10111T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925616 | ||||||
| chr19:53925666
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10161C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925666 | ||||||
| chr19:53925678
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+10173G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925678 | ||||||
| chr19:53925726
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.424+10221G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925726 | ||||||
| chr19:53925732
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.424+10227G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925732 | ||||||
| chr19:53925747
|
G | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0335 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+10242G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925747 | ||||||
| chr19:53925749
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+10244C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925749 | ||||||
| chr19:53925791
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.424+10286C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925791 | ||||||
| chr19:53925795
|
A | C | 1 | a0001c0001t0002g0264 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.424+10290A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925795 | ||||||
| chr19:53925892
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.424+10387A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925892 | ||||||
| chr19:53925930
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+10425C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925930 | ||||||
| chr19:53925944
|
G | T | 115 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.424+10439G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925944 | ||||||
| chr19:53925993
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+10488C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925993 | ||||||
| chr19:53926036
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0006g0351others(1): Show | 4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+10531A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926036 | ||||||
| chr19:53926151
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0004g0354 | 3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+10646A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926151 | ||||||
| chr19:53926163
|
C | G | 1 | a0001c0001t0015g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+10658C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926163 | ||||||
| chr19:53926196
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.424+10691A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926196 | ||||||
| chr19:53926206
|
T | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+10701T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926206 | ||||||
| chr19:53926237
|
G | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10732G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926237 | ||||||
| chr19:53926276
|
A | G | 1 | a0001c0001t0023g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.424+10771A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926276 | ||||||
| chr19:53926401
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0004g0217 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.424+10896C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926401 | ||||||
| chr19:53926435
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0004g0217 | 2 | HG03516.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.424+10930G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926435 | ||||||
| chr19:53926545
|
T | G | 16 | a0001c0001t0001g0168a0001c0001t0001g0188a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+11040T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926545 | ||||||
| chr19:53926640
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.424+11135C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926640 | ||||||
| chr19:53926710
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0086 | 2 | NA19064.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.424+11205C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926710 | ||||||
| chr19:53926723
|
G | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0111 | 3 | HG00438.hp1 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.424+11218G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926723 | ||||||
| chr19:53926750
|
T | TA | 8 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0003g0003others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+11250dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53926750 | |||||
| chr19:53926905
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0004g0354 | 2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+11400T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926905 | ||||||
| chr19:53926932
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0004g0354 | 2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+11427G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926932 | ||||||
| chr19:53927003
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0226others(6): Show | 10 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+11498C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927003 | ||||||
| chr19:53927022
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0090 | 3 | HG02155.hp2 NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.424+11517G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927022 | ||||||
| chr19:53927085
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(6): Show | 10 | HG01243.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+11580A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927085 | ||||||
| chr19:53927187
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+11682C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927187 | ||||||
| chr19:53927192
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.424+11687T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927192 | ||||||
| chr19:53927200
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.424+11695G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927200 | ||||||
| chr19:53927215
|
G | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(95): Show | 103 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.424+11710G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927215 | ||||||
| chr19:53927275
|
T | C | 1 | a0001c0001t0011g0349 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+11770T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927275 | ||||||
| chr19:53927414
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.424+11909C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927414 | ||||||
| chr19:53927425
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 113 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.424+11920C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927425 | ||||||
| chr19:53927510
|
A | G | 36 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 37 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+12005A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927510 | ||||||
| chr19:53927575
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(103): Show | 110 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.424+12070C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927575 | ||||||
| chr19:53927602
|
C | T | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 9 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+12097C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927602 | ||||||
| chr19:53927717
|
A | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 22 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+12212A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927717 | ||||||
| chr19:53927762
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 133 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.424+12257C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927762 | ||||||
| chr19:53927792
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 108 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.424+12287C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927792 | ||||||
| chr19:53927795
|
A | G | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+12290A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927795 | ||||||
| chr19:53927799
|
T | C | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+12294T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927799 | ||||||
| chr19:53927811
|
T | C | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(78): Show | 82 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.424+12306T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927811 | ||||||
| chr19:53927817
|
A | G | 51 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(48): Show | 53 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+12312A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927817 | ||||||
| chr19:53927838
|
C | CA | 89 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0035others(86): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.424+12348dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | |||||
| chr19:53927838
|
C | CAA | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12347_424+1234 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | |||||
| chr19:53927838
|
CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0087others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12335_424+1234 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | |||||
| chr19:53927840
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12335A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927840 | ||||||
| chr19:53927841
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12336A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927841 | ||||||
| chr19:53927845
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12340A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927845 | ||||||
| chr19:53927854
|
G | A | 1 | a0001c0001t0013g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+12349G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927854 | ||||||
| chr19:53927859
|
G | GA | 9 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0087others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12361dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927859 | |||||
| chr19:53927968
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 24 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.424+12463T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927968 | ||||||
| chr19:53928007
|
T | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 44 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+12502T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928007 | ||||||
| chr19:53928033
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 99 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.424+12528A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928033 | ||||||
| chr19:53928039
|
G | T | 3 | a0001c0001t0001g0065a0001c0001t0003g0027a0001c0001t0007g0067 | 3 | HG01884.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+12534G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928039 | ||||||
| chr19:53928043
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0003g0027a0001c0001t0007g0067 | 3 | HG01884.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+12538G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928043 | ||||||
| chr19:53928062
|
A | G | 143 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 145 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.424+12557A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928062 | ||||||
| chr19:53928073
|
GGA | G | 88 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(85): Show | 89 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.424+12571_424+1257 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928073 | |||||
| chr19:53928074
|
GA | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(61): Show | 67 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+12570delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928074 | ||||||
| chr19:53928077
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(61): Show | 67 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+12572A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928077 | ||||||
| chr19:53928202
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.424+12697G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928202 | ||||||
| chr19:53928261
|
GTATT | G | 17 | a0001c0001t0001g0061a0001c0001t0001g0197a0001c0001t0001g0198others(14): Show | 17 | HG01934.hp1 HG01978.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+12775_424+1277 others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928261 | |||||
| chr19:53928263
|
AT | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0087others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+12761delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928263 | |||||
| chr19:53928264
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(109): Show | 116 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.424+12759T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928264 | ||||||
| chr19:53928361
|
T | TC | 4 | a0001c0001t0001g0072a0001c0001t0004g0054a0001c0001t0004g0056others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+12857dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928361 | |||||
| chr19:53928366
|
G | A | 1 | a0001c0001t0016g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.424+12861G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928366 | ||||||
| chr19:53928485
|
G | C | 2 | a0001c0001t0002g0004a0001c0001t0013g0009 | 3 | HG01070.hp2 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.424+12980G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928485 | ||||||
| chr19:53928495
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-12975G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928495 | ||||||
| chr19:53928567
|
A | C | 37 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0049others(34): Show | 39 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.425-12903A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928567 | ||||||
| chr19:53928674
|
G | C | 165 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.425-12796G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928674 | ||||||
| chr19:53928818
|
TA | T | 2 | a0001c0001t0002g0004a0001c0001t0021g0068 | 3 | HG01070.hp2 HG01071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.425-12650delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928818 | |||||
| chr19:53928876
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.425-12594T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928876 | ||||||
| chr19:53928877
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-12593G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928877 | ||||||
| chr19:53928977
|
C | T | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-12493C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928977 | ||||||
| chr19:53929057
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.425-12413T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929057 | ||||||
| chr19:53929058
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(6): Show | 10 | HG01109.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-12412G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929058 | ||||||
| chr19:53929065
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-12405C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929065 | ||||||
| chr19:53929111
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425-12348_425-1233 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929111 | |||||
| chr19:53929117
|
AAAAAC | A | 15 | a0001c0001t0001g0085a0001c0001t0001g0125a0001c0001t0001g0128others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(9): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929117 | |||||
| chr19:53929118
|
AAAAC | A | 158 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929118 | |||||
| chr19:53929120
|
AAC | A | 12 | a0001c0001t0001g0059a0001c0001t0001g0198a0001c0001t0001g0200others(9): Show | 12 | HG00621.hp1 HG01934.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929120 | |||||
| chr19:53929121
|
AC | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0197a0001c0001t0001g0204others(1): Show | 4 | HG01978.hp1 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-12348delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929121 | ||||||
| chr19:53929122
|
C | CA | 16 | a0001c0001t0001g0032a0001c0001t0001g0098a0001c0001t0001g0141others(13): Show | 17 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-12332dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929122 | |||||
| chr19:53929122
|
C | CAAA | 9 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(6): Show | 10 | HG01109.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-12334_425-1233 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929122 | |||||
| chr19:53929160
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0101 | 2 | NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.425-12310G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929160 | ||||||
| chr19:53929263
|
TGAGAGAG others(7): Show |
T | 32 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(29): Show | 36 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-12192_425-1217 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929263 | |||||
| chr19:53929352
|
T | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(29): Show | 36 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-12118T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929352 | ||||||
| chr19:53929467
|
A | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(18): Show | 24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-12003A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929467 | ||||||
| chr19:53929633
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021 | 4 | HG01243.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-11837T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929633 | ||||||
| chr19:53929686
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.425-11784G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929686 | ||||||
| chr19:53929813
|
G | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0008g0025 | 3 | HG02145.hp1 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.425-11657G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929813 | ||||||
| chr19:53929955
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(221): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.425-11515A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929955 | ||||||
| chr19:53930074
|
C | CA | 170 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.425-11377dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | |||||
| chr19:53930074
|
C | CAA | 41 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(38): Show | 42 | HG00438.hp1 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.425-11378_425-1137 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | |||||
| chr19:53930074
|
C | CAAA | 9 | a0001c0001t0001g0008a0001c0001t0001g0074a0001c0001t0001g0157others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-11379_425-1137 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | |||||
| chr19:53930179
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.425-11291C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930179 | ||||||
| chr19:53930208
|
CCA | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0215others(5): Show | 9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-11261_425-1126 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930208 | ||||||
| chr19:53930210
|
A | AT | 20 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0030others(17): Show | 20 | HG01168.hp2 HG01261.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.425-11247dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930210 | |||||
| chr19:53930210
|
AT | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(32): Show | 38 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.425-11247delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930210 | |||||
| chr19:53930212
|
T | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0215others(5): Show | 9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-11258T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930212 | ||||||
| chr19:53930249
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(6): Show | 10 | HG01109.hp2 HG02055.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-11221C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930249 | ||||||
| chr19:53930312
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(23): Show | 30 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.425-11158A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930312 | ||||||
| chr19:53930333
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(22): Show | 29 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.425-11137C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930333 | ||||||
| chr19:53930384
|
T | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-11086T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930384 | ||||||
| chr19:53930395
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.425-11075C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930395 | ||||||
| chr19:53930467
|
GGTACACA others(25): Show |
G | 1 | a0001c0001t0018g0274 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.425-10999_425-1096 others(36): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930467 | |||||
| chr19:53930497
|
C | T | 1 | a0001c0001t0004g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-10973C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930497 | ||||||
| chr19:53930532
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(24): Show | 31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10938T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930532 | ||||||
| chr19:53930662
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-10808C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930662 | ||||||
| chr19:53930752
|
C | CCCT | 27 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(24): Show | 31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10716_425-1071 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930752 | |||||
| chr19:53930872
|
T | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.425-10598T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930872 | ||||||
| chr19:53930961
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 8 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-10509C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930961 | ||||||
| chr19:53931001
|
G | C | 1 | a0001c0001t0001g0355 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.425-10469G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931001 | ||||||
| chr19:53931008
|
C | A | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10462C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931008 | ||||||
| chr19:53931234
|
A | G | 1 | a0001c0001t0004g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-10236A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931234 | ||||||
| chr19:53931266
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(24): Show | 31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10204G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931266 | ||||||
| chr19:53931398
|
C | G | 1 | a0001c0001t0001g0291 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.425-10072C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931398 | ||||||
| chr19:53931453
|
G | A | 1 | a0001c0002t0002g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.425-10017G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931453 | ||||||
| chr19:53931462
|
A | G | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10008A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931462 | ||||||
| chr19:53931465
|
C | T | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10005C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931465 | ||||||
| chr19:53931547
|
G | T | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-9923G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931547 | ||||||
| chr19:53931615
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0018g0274 | 2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.425-9855G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931615 | ||||||
| chr19:53931684
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.425-9786C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931684 | ||||||
| chr19:53931685
|
T | TA | 82 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(79): Show | 84 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.425-9762dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | |||||
| chr19:53931685
|
T | TAA | 15 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0094others(12): Show | 15 | HG00639.hp1 HG00673.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.425-9763_425-9762d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | |||||
| chr19:53931685
|
T | TAAA | 9 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0144others(6): Show | 9 | HG00733.hp2 HG01070.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-9764_425-9762d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | |||||
| chr19:53931685
|
TAAAAAAA others(1): Show |
T | 10 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(7): Show | 12 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-9769_425-9762d others(10): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | |||||
| chr19:53931710
|
A | G | 1 | a0001c0001t0020g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.425-9760A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931710 | ||||||
| chr19:53931723
|
C | T | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-9747C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931723 | ||||||
| chr19:53931731
|
CACT | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(5): Show | 9 | HG01109.hp2 HG02055.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-9734_425-9732d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931731 | |||||
| chr19:53931759
|
C | CT | 56 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0030others(53): Show | 57 | HG00639.hp2 HG01123.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.425-9691dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931759 | |||||
| chr19:53931759
|
CT | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(4): Show | 8 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-9691delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931759 | |||||
| chr19:53931784
|
T | C | 2 | a0001c0001t0004g0193a0001c0001t0011g0349 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-9686T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931784 | ||||||
| chr19:53931855
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(24): Show | 31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-9615A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931855 | ||||||
| chr19:53931906
|
C | T | 1 | a0001c0001t0004g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-9564C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931906 | ||||||
| chr19:53931919
|
G | A | 11 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-9551G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931919 | ||||||
| chr19:53931969
|
G | C | 1 | a0001c0001t0021g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-9501G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931969 | ||||||
| chr19:53932018
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-9452T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932018 | ||||||
| chr19:53932036
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-9434C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932036 | ||||||
| chr19:53932056
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-9414C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932056 | ||||||
| chr19:53932168
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.425-9302G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932168 | ||||||
| chr19:53932224
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(16): Show | 22 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.425-9246A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932224 | ||||||
| chr19:53932252
|
T | TA | 14 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0001g0112others(11): Show | 14 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.425-9198dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | |||||
| chr19:53932252
|
TA | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0051others(10): Show | 13 | HG00323.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-9198delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | |||||
| chr19:53932252
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.425-9207_425-9198d others(12): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | |||||
| chr19:53932260
|
A | AG | 4 | a0001c0001t0001g0066a0001c0001t0001g0213a0001c0001t0007g0064others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-9210_425-9209i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932260 | ||||||
| chr19:53932331
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(17): Show | 23 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-9139C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932331 | ||||||
| chr19:53932466
|
C | CTGAGT | 18 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.425-9002_425-8998d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932466 | |||||
| chr19:53932576
|
C | T | 8 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG00099.hp1 HG02486.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-8894C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932576 | ||||||
| chr19:53932581
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425-8889T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932581 | ||||||
| chr19:53932636
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932636 | ||||||
| chr19:53932774
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.425-8696A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932774 | ||||||
| chr19:53932792
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0289 | 2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.425-8678G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932792 | ||||||
| chr19:53932830
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8640T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932830 | ||||||
| chr19:53932831
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0060others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-8639C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932831 | ||||||
| chr19:53932834
|
C | CT | 16 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0198others(13): Show | 16 | HG00621.hp1 HG01934.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-8619dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | |||||
| chr19:53932834
|
CT | C | 11 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(8): Show | 12 | HG01109.hp2 HG01168.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-8619delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | |||||
| chr19:53932834
|
CTTT | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0062others(2): Show | 6 | HG02145.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-8621_425-8619d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | |||||
| chr19:53932865
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.425-8605G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932865 | ||||||
| chr19:53932954
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8516T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932954 | ||||||
| chr19:53932966
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8504C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932966 | ||||||
| chr19:53932968
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0013g0009 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-8502C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932968 | ||||||
| chr19:53933048
|
C | T | 1 | a0001c0001t0023g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.425-8422C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933048 | ||||||
| chr19:53933089
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.425-8381T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933089 | ||||||
| chr19:53933110
|
A | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(18): Show | 24 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-8360A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933110 | ||||||
| chr19:53933182
|
ACTGCAAC others(16): Show |
A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.425-8263_425-8241d others(25): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933182 | |||||
| chr19:53933297
|
A | AT | 30 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0038others(27): Show | 30 | HG00544.hp1 HG00673.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.425-8152dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | |||||
| chr19:53933297
|
AT | A | 6 | a0001c0001t0001g0073a0001c0001t0001g0131a0001c0001t0001g0285others(3): Show | 6 | HG01099.hp2 HG01261.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-8152delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | |||||
| chr19:53933297
|
ATTT | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8154_425-8152d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | |||||
| chr19:53933374
|
G | A | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(352): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.425-8096G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933374 | ||||||
| chr19:53933424
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.425-8046T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933424 | ||||||
| chr19:53933655
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.425-7815G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933655 | ||||||
| chr19:53933661
|
A | AT | 10 | a0001c0001t0001g0022a0001c0001t0001g0197a0001c0001t0001g0248others(7): Show | 10 | HG01168.hp1 HG01978.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-7794dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933661 | |||||
| chr19:53933661
|
AT | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(6): Show | 10 | HG01243.hp2 HG01516.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-7794delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933661 | |||||
| chr19:53933896
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-7574T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933896 | ||||||
| chr19:53934058
|
C | T | 14 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(11): Show | 16 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-7412C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934058 | ||||||
| chr19:53934196
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(17): Show | 23 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-7274T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934196 | ||||||
| chr19:53934591
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.425-6879A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934591 | ||||||
| chr19:53934608
|
TA | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(9): Show | 13 | HG01099.hp1 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-6847delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53934608 | |||||
| chr19:53934827
|
GA | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0084others(9): Show | 12 | HG03669.hp2 HG03831.hp2 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-6632delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53934827 | |||||
| chr19:53934848
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-6622G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934848 | ||||||
| chr19:53934864
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-6606A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934864 | ||||||
| chr19:53935071
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-6399C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935071 | ||||||
| chr19:53935082
|
C | CAT | 23 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(20): Show | 26 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-6382_425-6381d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935082 | |||||
| chr19:53935174
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.425-6296T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935174 | ||||||
| chr19:53935323
|
C | CT | 7 | a0001c0001t0001g0039a0001c0001t0001g0170a0001c0001t0001g0334others(4): Show | 7 | HG00544.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-6132dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935323 | |||||
| chr19:53935323
|
CT | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0288others(3): Show | 6 | HG01099.hp1 HG02015.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-6132delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935323 | |||||
| chr19:53935490
|
T | G | 1 | a0001c0001t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425-5980T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935490 | ||||||
| chr19:53935588
|
ACTGGGAT others(311): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.425-5863_425-5546d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935588 | |||||
| chr19:53935613
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0004g0193a0001c0001t0011g0349 | 4 | HG01070.hp2 HG01071.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-5857G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935613 | ||||||
| chr19:53935634
|
C | CTTT | 12 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0131others(9): Show | 13 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-5815_425-5813d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | |||||
| chr19:53935634
|
C | CTTTT | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.425-5816_425-5813d others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | |||||
| chr19:53935634
|
C | CTTTTT | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(84): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.425-5817_425-5813d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | |||||
| chr19:53935634
|
C | CTTTTTT | 8 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0181others(5): Show | 8 | HG01192.hp2 HG01515.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-5818_425-5813d others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | |||||
| chr19:53935764
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.425-5706C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935764 | ||||||
| chr19:53935800
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0003g0027 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.425-5670C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935800 | ||||||
| chr19:53935850
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.425-5620A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935850 | ||||||
| chr19:53935962
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.425-5508A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935962 | ||||||
| chr19:53935980
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0021others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-5490A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935980 | ||||||
| chr19:53935996
|
C | T | 2 | a0001c0001t0014g0208a0001c0001t0019g0281 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.425-5474C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935996 | ||||||
| chr19:53936031
|
C | T | 10 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-5439C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936031 | ||||||
| chr19:53936148
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.425-5322G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936148 | ||||||
| chr19:53936205
|
G | C | 1 | a0001c0001t0002g0182 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.425-5265G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936205 | ||||||
| chr19:53936278
|
A | G | 6 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0002g0004others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-5192A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936278 | ||||||
| chr19:53936279
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.425-5191G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936279 | ||||||
| chr19:53936280
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0002g0004others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-5190G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936280 | ||||||
| chr19:53936429
|
C | T | 60 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0035others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.425-5041C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936429 | ||||||
| chr19:53936660
|
T | G | 5 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0004g0193others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4810T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936660 | ||||||
| chr19:53936701
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0179 | 2 | NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.425-4769T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936701 | ||||||
| chr19:53936845
|
G | A | 11 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-4625G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936845 | ||||||
| chr19:53936879
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0307 | 2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.425-4591G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936879 | ||||||
| chr19:53936905
|
A | C | 1 | a0001c0001t0002g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.425-4565A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936905 | ||||||
| chr19:53936969
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425-4501G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936969 | ||||||
| chr19:53937090
|
A | G | 1 | a0001c0001t0025g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-4380A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937090 | ||||||
| chr19:53937156
|
C | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-4314C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937156 | ||||||
| chr19:53937161
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0307 | 2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.425-4309A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937161 | ||||||
| chr19:53937193
|
A | G | 1 | a0001c0001t0014g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.425-4277A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937193 | ||||||
| chr19:53937220
|
C | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.425-4250C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937220 | ||||||
| chr19:53937397
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-4073A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937397 | ||||||
| chr19:53937406
|
T | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0004g0193others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4064T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937406 | ||||||
| chr19:53937568
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.425-3902C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937568 | ||||||
| chr19:53937569
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0005g0055 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.425-3901C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937569 | ||||||
| chr19:53937576
|
TCCCTC | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(316): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.425-3867_425-3863d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53937576 | |||||
| chr19:53937605
|
T | A | 4 | a0001c0001t0002g0110a0001c0001t0002g0302a0001c0001t0002g0317others(1): Show | 4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-3865T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937605 | ||||||
| chr19:53937654
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0014g0208 | 2 | HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.425-3816G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937654 | ||||||
| chr19:53937682
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0060others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-3788C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937682 | ||||||
| chr19:53937727
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(322): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3743G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937727 | ||||||
| chr19:53937746
|
G | A | 1 | a0001c0001t0019g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.425-3724G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937746 | ||||||
| chr19:53937883
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.425-3587G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937883 | ||||||
| chr19:53937946
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(322): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3524T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937946 | ||||||
| chr19:53938074
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-3396T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938074 | ||||||
| chr19:53938145
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.425-3325G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938145 | ||||||
| chr19:53938209
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-3261A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938209 | ||||||
| chr19:53938246
|
T | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(322): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3224T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938246 | ||||||
| chr19:53938397
|
G | T | 29 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0059others(26): Show | 30 | HG00621.hp1 HG00673.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-3073G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938397 | ||||||
| chr19:53938427
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-3043G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938427 | ||||||
| chr19:53938481
|
G | A | 1 | a0001c0001t0021g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-2989G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938481 | ||||||
| chr19:53938536
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-2934G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938536 | ||||||
| chr19:53938565
|
A | T | 1 | a0001c0001t0009g0158 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.425-2905A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938565 | ||||||
| chr19:53938804
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0021g0068a0001c0002t0002g0019 | 4 | HG01070.hp2 HG01071.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2666C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938804 | ||||||
| chr19:53938847
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.425-2623C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938847 | ||||||
| chr19:53938947
|
TCAAAA | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-2502_425-2498d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53938947 | |||||
| chr19:53939149
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.425-2321G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939149 | ||||||
| chr19:53939198
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.425-2272C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939198 | ||||||
| chr19:53939408
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.425-2062C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939408 | ||||||
| chr19:53939693
|
C | G | 1 | a0001c0001t0003g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-1777C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939693 | ||||||
| chr19:53939717
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0013g0009 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-1753G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939717 | ||||||
| chr19:53939779
|
T | G | 2 | a0001c0001t0002g0015a0001c0001t0013g0009 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-1691T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939779 | ||||||
| chr19:53939797
|
G | A | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.425-1673G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939797 | ||||||
| chr19:53940040
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.425-1430C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940040 | ||||||
| chr19:53940162
|
A | G | 2 | a0001c0001t0003g0023a0001c0001t0005g0348 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.425-1308A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940162 | ||||||
| chr19:53940611
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.425-859A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940611 | ||||||
| chr19:53940612
|
T | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(320): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.425-858T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940612 | ||||||
| chr19:53940627
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.425-843C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940627 | ||||||
| chr19:53940642
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.425-828T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940642 | ||||||
| chr19:53940777
|
G | A | 1 | a0001c0001t0008g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.425-693G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940777 | ||||||
| chr19:53940781
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0297a0001c0001t0002g0015others(1): Show | 4 | HG01109.hp1 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-689G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940781 | ||||||
| chr19:53940857
|
C | A | 1 | a0001c0001t0002g0264 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.425-613C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940857 | ||||||
| chr19:53940863
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG01891.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.425-607T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940863 | ||||||
| chr19:53940900
|
TA | T | 11 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-559delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53940900 | |||||
| chr19:53940918
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.425-552G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940918 | ||||||
| chr19:53940929
|
C | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0114others(4): Show | 7 | HG00140.hp1 HG01099.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-541C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940929 | ||||||
| chr19:53940933
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0294 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.425-537C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940933 | ||||||
| chr19:53940934
|
G | A | 2 | a0001c0001t0007g0064a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.425-536G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940934 | ||||||
| chr19:53941017
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0215others(4): Show | 8 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-453G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53941017 | ||||||
| chr19:53941061
|
CA | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(320): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.425-396delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53941061 | |||||
| chr19:53941670
|
G | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+55G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941670 | ||||||
| chr19:53941671
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+56C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941671 | ||||||
| chr19:53941691
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0340 | 2 | NA18957.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.570+76G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941691 | ||||||
| chr19:53941712
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.570+97A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941712 | ||||||
| chr19:53941882
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.571-154C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941882 | ||||||
| chr19:53942026
|
C | T | 2 | a0001c0001t0007g0064a0001c0001t0007g0067 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.571-10C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53942026 |