| geneid | 10368 |
|---|---|
| ensemblid | ENSG00000006116.4 |
| hgncid | 1407 |
| symbol | CACNG3 |
| name | calcium voltage-gated channel auxiliary subunit gamma 3 |
| refseq_nuc | NM_006539.4 |
| refseq_prot | NP_006530.1 |
| ensembl_nuc | ENST00000005284.4 |
| ensembl_prot | ENSP00000005284.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 24256335 |
| end | 24362412 |
| strand | + |
| ver | v1.2 |
| region | chr16:24256335-24362412 |
| region5000 | chr16:24251335-24367412 |
| regionname0 | CACNG3_chr16_24256335_24362412 |
| regionname5000 | CACNG3_chr16_24251335_24367412 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 315 | 366 | 90 | 68 | 150 | 14 | 42 | 110 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 948 | 360 | 87 | 68 | 150 | 14 | 39 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| c0002 | 0/0 | 948 | 5 | 2 | 0 | 0 | 0 | 3 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| c0003 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 970 | 324 | 76 | 63 | 139 | 12 | 33 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| t0002 | 0/1 | 971 | 32 | 6 | 4 | 10 | 2 | 9 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| t0003 | 0/0 | 970 | 5 | 5 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| t0004 | 0/0 | 970 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| t0005 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| t0006 | 0/0 | 970 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 948 | 360 | 87 | 68 | 150 | 14 | 39 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0002 | 0/0 | 948 | 5 | 2 | 0 | 0 | 0 | 3 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0003 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1917 | 318 | 73 | 63 | 139 | 12 | 30 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0001t0002 | 0/1 | 1918 | 32 | 6 | 4 | 10 | 2 | 9 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0001t0003 | 0/0 | 1917 | 5 | 5 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0001t0004 | 0/0 | 1917 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0001t0005 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0001t0006 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0002t0001 | 0/0 | 1917 | 5 | 2 | 0 | 0 | 0 | 3 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| a0001c0003t0001 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | copy fasta | chr16 | 24251335 | 24367412 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0002g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | GBR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0313 | EUR | GBR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | FIN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0053 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | IBS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | IBS | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CDX | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0331 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0361 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0237 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | STU | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0332 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ASW | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ASW | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | GIH | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | GIH | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | USA | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0334 | AFR | USA | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | USA | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0352 | REF | REF | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | CACNG3_chr16_24251335_24367412 | CACNG3 | chr16 | 24251335 | 24367412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24361686
|
C | T | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.771C>T | p.Ile257Ile | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 4/4 | 1191/1917 | 771/948 | 257/315 | chr16 | 24361686 | ||
| chr16:24361836
|
G | A | 1 | a0001c0002 | 5 | HG02109.hp1 HG02280.hp1 HG03669.hp1 others(2): Show |
synonymous_variant | LOW | c.921G>A | p.Pro307Pro | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 4/4 | 1341/1917 | 921/948 | 307/315 | chr16 | 24361836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24256382
|
G | A | 1 | a0001c0001t0004 | 3 | HG02258.hp1 HG06807.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-373G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/4 | 373 | chr16 | 24256382 | |||||
| chr16:24256531
|
C | T | 1 | a0001c0001t0006 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-224C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/4 | 224 | chr16 | 24256531 | |||||
| chr16:24362067
|
C | CT | 1 | a0001c0001t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*206dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 4/4 | 207 | INFO_REALIGN_3_PRIME | chr16 | 24362067 | ||||
| chr16:24362198
|
G | A | 1 | a0001c0001t0003 | 5 | HG02630.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 4/4 | 335 | chr16 | 24362198 | |||||
| chr16:24362221
|
G | A | 1 | a0001c0001t0005 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 4/4 | 358 | chr16 | 24362221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24256974
|
A | G | 4 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+9A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24256974 | ||||||
| chr16:24256975
|
A | C | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0002t0001g0361 | 3 | HG02280.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+10A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24256975 | ||||||
| chr16:24257179
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+214G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257179 | ||||||
| chr16:24257259
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0302a0001c0001t0001g0303others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.211+294A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257259 | ||||||
| chr16:24257284
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+319G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257284 | ||||||
| chr16:24257356
|
A | G | 365 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.211+391A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257356 | ||||||
| chr16:24257363
|
A | AG | 11 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(8): Show | 11 | HG00558.hp2 HG01243.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+404dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257363 | |||||
| chr16:24257367
|
GGGA | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00735.hp2 HG01256.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.211+404_211+406del others(3): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257367
|
GGGAGAGA others(4): Show |
G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.211+404_211+414del others(11): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257367
|
GGGAGAGA others(6): Show |
G | 1 | a0001c0001t0001g0012 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.211+404_211+416del others(13): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257367
|
GGGAGAGA others(8): Show |
G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211+404_211+418del others(15): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257367
|
GGGAGAGA others(10): Show |
G | 1 | a0001c0001t0001g0014 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.211+404_211+420del others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257367
|
GGGAGAGA others(18): Show |
G | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.211+404_211+428del others(25): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257367 | |||||
| chr16:24257368
|
G | GGA | 19 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.211+462_211+463dup others(2): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGA | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+460_211+463dup others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGAGA | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG01978.hp1 HG01981.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.211+458_211+463dup others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGAGAG others(1): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(3): Show | 6 | HG00423.hp2 HG01109.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+456_211+463dup others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGAGAG others(3): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+454_211+463dup others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGAGAG others(5): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.211+452_211+463dup others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGAGAGAG others(7): Show |
1 | a0001c0001t0001g0016 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.211+450_211+463dup others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGGGAGAG others(3): Show |
1 | a0001c0001t0001g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.211+404_211+405ins others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGGGAGAG others(7): Show |
1 | a0001c0001t0001g0300 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+404_211+405ins others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
G | GGGGGAGA others(6): Show |
1 | a0001c0001t0001g0335 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211+404_211+405ins others(13): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGA | G | 20 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(17): Show | 20 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+462_211+463del others(2): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGA | G | 18 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(15): Show | 18 | HG00642.hp2 HG01070.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.211+460_211+463del others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGA | G | 22 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(19): Show | 22 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.211+458_211+463del others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(1): Show |
G | 27 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(24): Show | 27 | HG00735.hp1 HG01069.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.211+456_211+463del others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(3): Show |
G | 14 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0193others(11): Show | 14 | HG01934.hp2 HG02109.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+454_211+463del others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(5): Show |
G | 8 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(5): Show | 8 | HG00738.hp2 HG01169.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+452_211+463del others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(7): Show |
G | 25 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.211+450_211+463del others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(9): Show |
G | 25 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(22): Show | 25 | HG00423.hp1 HG01358.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.211+448_211+463del others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(11): Show |
G | 14 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(11): Show | 14 | HG00408.hp2 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+446_211+463del others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(13): Show |
G | 13 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(10): Show | 13 | HG02027.hp1 HG02165.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.211+444_211+463del others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(15): Show |
G | 2 | a0001c0001t0001g0282a0001c0001t0002g0283 | 2 | HG01175.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.211+442_211+463del others(22): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(17): Show |
G | 4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0287others(1): Show | 4 | HG01433.hp2 HG03098.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+440_211+463del others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257368
|
GGAGAGAG others(19): Show |
G | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.211+438_211+463del others(26): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24257368 | |||||
| chr16:24257369
|
GA | G | 6 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(3): Show | 6 | HG00673.hp1 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+405delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257369
|
GAGAGA | G | 3 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0002g0352 | 3 | NA19054.hp1 NA19070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.211+405_211+409del others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257369
|
GAGAGAGA others(4): Show |
G | 1 | a0001c0001t0001g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.211+405_211+415del others(11): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257369
|
GAGAGAGA others(6): Show |
G | 2 | a0001c0001t0001g0001a0001c0001t0001g0291 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.211+405_211+417del others(13): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257369
|
GAGAGAGA others(10): Show |
G | 6 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 6 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+405_211+421del others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257369
|
GAGAGAGA others(12): Show |
G | 2 | a0001c0001t0001g0299a0001c0001t0003g0298 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.211+405_211+423del others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257369 | ||||||
| chr16:24257370
|
A | G | 18 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(15): Show | 18 | HG00544.hp1 HG00558.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+405A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257370 | ||||||
| chr16:24257372
|
A | G | 10 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(7): Show | 10 | HG00544.hp1 HG00673.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+407A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257372 | ||||||
| chr16:24257374
|
A | G | 5 | a0001c0001t0001g0324a0001c0001t0001g0330a0001c0001t0001g0358others(2): Show | 5 | HG01993.hp2 HG03710.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+409A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257374 | ||||||
| chr16:24257376
|
A | G | 3 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0002g0352 | 3 | NA19054.hp1 NA19070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.211+411A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257376 | ||||||
| chr16:24257378
|
A | G | 5 | a0001c0001t0001g0301a0001c0001t0001g0322a0001c0001t0001g0323others(2): Show | 5 | HG02258.hp1 HG02818.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+413A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257378 | ||||||
| chr16:24257380
|
A | G | 2 | a0001c0001t0001g0321a0001c0001t0004g0334 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.211+415A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257380 | ||||||
| chr16:24257382
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.211+417A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257382 | ||||||
| chr16:24257384
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+419A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257384 | ||||||
| chr16:24257386
|
A | G | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0002t0001g0361 | 3 | HG02280.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+421A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257386 | ||||||
| chr16:24257420
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211+455A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257420 | ||||||
| chr16:24257855
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.211+890A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257855 | ||||||
| chr16:24257856
|
T | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0302others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.211+891T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257856 | ||||||
| chr16:24257966
|
C | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.211+1001C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24257966 | ||||||
| chr16:24258061
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211+1096G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258061 | ||||||
| chr16:24258291
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.211+1326G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258291 | ||||||
| chr16:24258337
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.211+1372G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258337 | ||||||
| chr16:24258526
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0166 | 2 | HG00408.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.211+1561T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258526 | ||||||
| chr16:24258850
|
A | G | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+1885A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258850 | ||||||
| chr16:24258867
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.211+1902A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258867 | ||||||
| chr16:24258923
|
C | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(8): Show | 11 | HG00741.hp2 HG01258.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+1958C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24258923 | ||||||
| chr16:24259051
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0084 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.211+2086G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259051 | ||||||
| chr16:24259086
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.211+2121T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259086 | ||||||
| chr16:24259265
|
T | A | 1 | a0001c0001t0001g0327 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211+2300T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259265 | ||||||
| chr16:24259738
|
C | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.211+2773C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259738 | ||||||
| chr16:24259741
|
G | A | 2 | a0001c0001t0001g0322a0001c0001t0001g0355 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.211+2776G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259741 | ||||||
| chr16:24259799
|
G | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0107a0001c0002t0001g0009 | 3 | HG01346.hp1 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.211+2834G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259799 | ||||||
| chr16:24259841
|
A | G | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+2876A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259841 | ||||||
| chr16:24259904
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.211+2939A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24259904 | ||||||
| chr16:24260285
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.211+3320C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260285 | ||||||
| chr16:24260729
|
A | T | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+3764A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260729 | ||||||
| chr16:24260736
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(256): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.211+3771T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260736 | ||||||
| chr16:24260802
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.211+3837G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260802 | ||||||
| chr16:24260878
|
G | A | 4 | a0001c0001t0001g0304a0001c0001t0001g0326a0001c0001t0001g0336others(1): Show | 4 | HG00639.hp1 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3913G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260878 | ||||||
| chr16:24260922
|
A | C | 1 | a0001c0001t0001g0281 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.211+3957A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24260922 | ||||||
| chr16:24261039
|
T | G | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+4074T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261039 | ||||||
| chr16:24261045
|
T | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.211+4080T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261045 | ||||||
| chr16:24261064
|
G | T | 170 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.211+4099G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261064 | ||||||
| chr16:24261242
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.211+4277C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261242 | ||||||
| chr16:24261335
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+4370G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261335 | ||||||
| chr16:24261458
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.211+4493A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24261458 | ||||||
| chr16:24262584
|
A | G | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+5619A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24262584 | ||||||
| chr16:24262653
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.211+5688C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24262653 | ||||||
| chr16:24262752
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+5787A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24262752 | ||||||
| chr16:24262792
|
T | C | 94 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(91): Show | 94 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.211+5827T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24262792 | ||||||
| chr16:24262804
|
A | G | 61 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.211+5839A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24262804 | ||||||
| chr16:24263070
|
A | G | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.211+6105A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263070 | ||||||
| chr16:24263282
|
A | C | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.211+6317A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263282 | ||||||
| chr16:24263322
|
T | C | 57 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.211+6357T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263322 | ||||||
| chr16:24263460
|
C | G | 76 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.211+6495C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263460 | ||||||
| chr16:24263484
|
T | C | 4 | a0001c0001t0001g0333a0001c0001t0004g0331a0001c0001t0004g0332others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6519T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263484 | ||||||
| chr16:24263831
|
A | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0281 | 2 | NA18960.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.211+6866A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263831 | ||||||
| chr16:24263955
|
GATT | G | 4 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6991_211+6993d others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24263955 | ||||||
| chr16:24264067
|
A | T | 170 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.211+7102A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264067 | ||||||
| chr16:24264148
|
C | A | 1 | a0001c0001t0001g0300 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+7183C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264148 | ||||||
| chr16:24264277
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+7312T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264277 | ||||||
| chr16:24264334
|
C | T | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+7369C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264334 | ||||||
| chr16:24264382
|
T | C | 15 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(12): Show | 15 | HG00280.hp2 HG02280.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+7417T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264382 | ||||||
| chr16:24264429
|
G | C | 4 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+7464G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264429 | ||||||
| chr16:24264575
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.211+7610C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264575 | ||||||
| chr16:24264607
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+7642C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264607 | ||||||
| chr16:24264608
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0002g0022 | 3 | NA18970.hp1 NA18974.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.211+7643G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264608 | ||||||
| chr16:24264677
|
A | C | 10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+7712A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24264677 | ||||||
| chr16:24265076
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0204others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+8111C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265076 | ||||||
| chr16:24265205
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0209 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.211+8240G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265205 | ||||||
| chr16:24265267
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0179 | 2 | HG03654.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.211+8302G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265267 | ||||||
| chr16:24265278
|
G | GGAAGGAA others(25): Show |
10 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+8323_211+8354d others(34): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265278 | |||||
| chr16:24265350
|
G | GGAAA | 240 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(237): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.211+8402_211+8405d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265350 | |||||
| chr16:24265370
|
A | AG | 3 | a0001c0001t0004g0331a0001c0001t0004g0332a0001c0001t0004g0334 | 3 | HG02258.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.211+8405_211+8406i others(3): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265370 | ||||||
| chr16:24265374
|
G | A | 4 | a0001c0001t0001g0333a0001c0001t0004g0331a0001c0001t0004g0332others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+8409G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265374 | ||||||
| chr16:24265447
|
A | AAGAG | 357 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(354): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.211+8483_211+8484i others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265447 | |||||
| chr16:24265449
|
A | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0363a0001c0001t0001g0364others(3): Show | 6 | HG00280.hp2 HG02129.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+8484A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265449 | ||||||
| chr16:24265455
|
G | GA | 5 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0365others(2): Show | 5 | HG00280.hp2 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+8492dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265455 | |||||
| chr16:24265469
|
G | GGA | 57 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.211+8517_211+8518d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265469 | |||||
| chr16:24265501
|
A | AAAAG | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.211+8555_211+8558d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24265501 | |||||
| chr16:24265562
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211+8597T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265562 | ||||||
| chr16:24265839
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0209 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.211+8874T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265839 | ||||||
| chr16:24265851
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.211+8886G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24265851 | ||||||
| chr16:24266256
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.211+9291C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266256 | ||||||
| chr16:24266276
|
C | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0152a0001c0001t0001g0168others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.211+9311C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266276 | ||||||
| chr16:24266318
|
T | G | 57 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.211+9353T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266318 | ||||||
| chr16:24266353
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+9388C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266353 | ||||||
| chr16:24266497
|
G | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+9532G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266497 | ||||||
| chr16:24266527
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG00558.hp1 NA18941.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.211+9562A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266527 | ||||||
| chr16:24266912
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.211+9947C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24266912 | ||||||
| chr16:24266968
|
C | CT | 7 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0144others(4): Show | 7 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+10019dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24266968 | |||||
| chr16:24266968
|
C | CTTTT | 14 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+10016_211+1001 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24266968 | |||||
| chr16:24266968
|
CT | C | 9 | a0001c0001t0001g0088a0001c0001t0001g0169a0001c0001t0001g0222others(6): Show | 9 | HG01168.hp2 HG01515.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+10019delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24266968 | |||||
| chr16:24267022
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0223a0001c0001t0002g0251 | 3 | HG02109.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.211+10057G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267022 | ||||||
| chr16:24267051
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.211+10086C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267051 | ||||||
| chr16:24267168
|
G | A | 1 | a0001c0001t0001g0358 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.211+10203G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267168 | ||||||
| chr16:24267209
|
G | A | 57 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0302others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.211+10244G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267209 | ||||||
| chr16:24267231
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+10266G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267231 | ||||||
| chr16:24267252
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+10287C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267252 | ||||||
| chr16:24267261
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.211+10296T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267261 | ||||||
| chr16:24267366
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.211+10401C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267366 | ||||||
| chr16:24267449
|
A | G | 79 | a0001c0001t0001g0115a0001c0001t0001g0189a0001c0001t0001g0222others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.211+10484A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267449 | ||||||
| chr16:24267472
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+10507G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267472 | ||||||
| chr16:24267883
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211+10918C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267883 | ||||||
| chr16:24267884
|
T | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0106a0001c0001t0001g0147others(19): Show | 22 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.211+10919T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267884 | ||||||
| chr16:24267957
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(260): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.211+10992T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267957 | ||||||
| chr16:24267961
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.211+10996G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24267961 | ||||||
| chr16:24268021
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+11056C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268021 | ||||||
| chr16:24268056
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.211+11091T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268056 | ||||||
| chr16:24268087
|
TGA | T | 52 | a0001c0001t0001g0280a0001c0001t0001g0302a0001c0001t0001g0303others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.211+11127_211+1112 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24268087 | |||||
| chr16:24268103
|
C | T | 1 | a0001c0001t0003g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+11138C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268103 | ||||||
| chr16:24268124
|
A | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0222a0001c0001t0001g0290others(12): Show | 15 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+11159A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268124 | ||||||
| chr16:24268379
|
A | G | 2 | a0001c0001t0001g0044a0001c0002t0001g0105 | 2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.211+11414A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268379 | ||||||
| chr16:24268580
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.211+11615T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268580 | ||||||
| chr16:24268782
|
G | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(267): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.211+11817G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24268782 | ||||||
| chr16:24269064
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0156others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.211+12099T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269064 | ||||||
| chr16:24269074
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0156others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.211+12109T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269074 | ||||||
| chr16:24269104
|
G | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.211+12139G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269104 | ||||||
| chr16:24269236
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0363a0001c0001t0001g0364others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+12271T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269236 | ||||||
| chr16:24269329
|
A | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.211+12364A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269329 | ||||||
| chr16:24269474
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.211+12509G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269474 | ||||||
| chr16:24269592
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+12627G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269592 | ||||||
| chr16:24269613
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211+12648G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269613 | ||||||
| chr16:24269621
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+12656C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269621 | ||||||
| chr16:24269708
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0257 | 2 | HG02015.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.211+12743T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269708 | ||||||
| chr16:24269746
|
C | CA | 23 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0089others(20): Show | 23 | HG00642.hp1 HG00673.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.211+12802dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24269746 | |||||
| chr16:24269746
|
CA | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.211+12802delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24269746 | |||||
| chr16:24269746
|
CAA | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0118a0001c0001t0001g0185others(4): Show | 7 | HG01069.hp1 HG01070.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+12801_211+1280 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24269746 | |||||
| chr16:24269787
|
A | AAAAG | 9 | a0001c0001t0001g0222a0001c0001t0001g0290a0001c0001t0001g0291others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+12840_211+1284 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24269787 | |||||
| chr16:24269863
|
GT | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0107others(5): Show | 8 | HG01346.hp1 HG01346.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+12909delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24269863 | |||||
| chr16:24269953
|
G | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0222a0001c0001t0001g0280others(65): Show | 68 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.211+12988G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24269953 | ||||||
| chr16:24270125
|
T | C | 5 | a0001c0001t0001g0324a0001c0001t0001g0328a0001c0001t0001g0337others(2): Show | 5 | HG00673.hp1 HG02165.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+13160T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270125 | ||||||
| chr16:24270185
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.211+13220C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270185 | ||||||
| chr16:24270189
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0093others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+13224T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270189 | ||||||
| chr16:24270354
|
C | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG02080.hp2 HG02132.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+13389C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270354 | ||||||
| chr16:24270776
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0363a0001c0001t0001g0364others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+13811T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270776 | ||||||
| chr16:24270929
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0183 | 2 | HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.211+13964C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270929 | ||||||
| chr16:24270939
|
T | G | 1 | a0001c0001t0002g0022 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.211+13974T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24270939 | ||||||
| chr16:24271132
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(265): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.211+14167A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271132 | ||||||
| chr16:24271161
|
T | A | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+14196T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271161 | ||||||
| chr16:24271162
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+14197G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271162 | ||||||
| chr16:24271260
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0002g0191 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.211+14295C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271260 | ||||||
| chr16:24271278
|
G | A | 68 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(65): Show | 68 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.211+14313G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271278 | ||||||
| chr16:24271284
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.211+14319G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271284 | ||||||
| chr16:24271301
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(265): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.211+14336T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271301 | ||||||
| chr16:24271333
|
G | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0267 | 2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.211+14368G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271333 | ||||||
| chr16:24271337
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0363a0001c0001t0001g0364others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+14372G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271337 | ||||||
| chr16:24271349
|
T | C | 4 | a0001c0001t0001g0241a0001c0001t0001g0260a0001c0001t0001g0346others(1): Show | 4 | HG00558.hp2 NA18946.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+14384T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271349 | ||||||
| chr16:24271523
|
A | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0100others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+14558A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271523 | ||||||
| chr16:24271648
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.211+14683T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271648 | ||||||
| chr16:24271742
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0134 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.211+14777C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271742 | ||||||
| chr16:24271754
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+14789G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24271754 | ||||||
| chr16:24271860
|
TC | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(266): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.211+14900delC | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24271860 | |||||
| chr16:24272040
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0210others(8): Show | 11 | HG01361.hp2 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+15075A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272040 | ||||||
| chr16:24272061
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.211+15096A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272061 | ||||||
| chr16:24272089
|
TTC | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0223a0001c0001t0002g0251 | 3 | HG02109.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.211+15134_211+1513 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24272089 | |||||
| chr16:24272101
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.211+15136T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272101 | ||||||
| chr16:24272122
|
TA | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0021others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.211+15167delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24272122 | |||||
| chr16:24272360
|
C | T | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0002t0001g0361 | 3 | HG02280.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+15395C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272360 | ||||||
| chr16:24272405
|
A | AT | 5 | a0001c0001t0001g0324a0001c0001t0001g0328a0001c0001t0001g0337others(2): Show | 5 | HG00673.hp1 HG02165.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+15442dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24272405 | |||||
| chr16:24272472
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.211+15507T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272472 | ||||||
| chr16:24272609
|
A | T | 54 | a0001c0001t0001g0169a0001c0001t0001g0280a0001c0001t0001g0294others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.211+15644A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272609 | ||||||
| chr16:24272682
|
A | T | 124 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.211+15717A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272682 | ||||||
| chr16:24272729
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+15764T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272729 | ||||||
| chr16:24272815
|
C | T | 55 | a0001c0001t0001g0169a0001c0001t0001g0280a0001c0001t0001g0294others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.211+15850C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272815 | ||||||
| chr16:24272870
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+15905G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24272870 | ||||||
| chr16:24273049
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(192): Show | 195 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.211+16084A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273049 | ||||||
| chr16:24273169
|
C | G | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0002t0001g0361 | 3 | HG02280.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+16204C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273169 | ||||||
| chr16:24273186
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211+16221C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273186 | ||||||
| chr16:24273365
|
T | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(64): Show | 67 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.211+16400T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273365 | ||||||
| chr16:24273457
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.211+16492A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273457 | ||||||
| chr16:24273504
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+16539T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273504 | ||||||
| chr16:24273600
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+16635C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273600 | ||||||
| chr16:24273887
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.211+16922A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24273887 | ||||||
| chr16:24274053
|
G | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0041others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.211+17088G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274053 | ||||||
| chr16:24274165
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+17200C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274165 | ||||||
| chr16:24274186
|
CA | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0047others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.211+17235delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24274186 | |||||
| chr16:24274187
|
AAAAAAAA others(7): Show |
A | 14 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(11): Show | 14 | HG01358.hp1 HG03017.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+17235_211+1724 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24274187 | |||||
| chr16:24274199
|
A | C | 2 | a0001c0001t0001g0354a0001c0001t0001g0363 | 2 | HG02970.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.211+17234A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274199 | ||||||
| chr16:24274200
|
A | C | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.211+17235A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274200 | ||||||
| chr16:24274201
|
C | A | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(97): Show | 100 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.211+17236C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274201 | ||||||
| chr16:24274304
|
GT | G | 4 | a0001c0001t0001g0287a0001c0001t0001g0363a0001c0001t0001g0364others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+17340delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274304 | ||||||
| chr16:24274357
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+17392G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274357 | ||||||
| chr16:24274550
|
C | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.211+17585C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274550 | ||||||
| chr16:24274591
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.211+17626C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274591 | ||||||
| chr16:24274630
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.211+17665A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274630 | ||||||
| chr16:24274668
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.211+17703G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274668 | ||||||
| chr16:24274669
|
A | C | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 115 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.211+17704A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274669 | ||||||
| chr16:24274728
|
A | C | 1 | a0001c0001t0001g0349 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.211+17763A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274728 | ||||||
| chr16:24274884
|
C | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+17919C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274884 | ||||||
| chr16:24274911
|
A | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(244): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.211+17946A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274911 | ||||||
| chr16:24274943
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+17978T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274943 | ||||||
| chr16:24274986
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.211+18021G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24274986 | ||||||
| chr16:24275053
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+18088C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275053 | ||||||
| chr16:24275082
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+18117G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275082 | ||||||
| chr16:24275158
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0004g0331 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.211+18193G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275158 | ||||||
| chr16:24275194
|
CA | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.211+18240delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24275194 | |||||
| chr16:24275197
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0005g0008 | 2 | NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.211+18232A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275197 | ||||||
| chr16:24275336
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0041others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.211+18371C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275336 | ||||||
| chr16:24275338
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(357): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.211+18373T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275338 | ||||||
| chr16:24275518
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.211+18553A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275518 | ||||||
| chr16:24275567
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211+18602A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275567 | ||||||
| chr16:24275839
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+18874G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275839 | ||||||
| chr16:24275975
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.211+19010T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24275975 | ||||||
| chr16:24276057
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.211+19092C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276057 | ||||||
| chr16:24276094
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.211+19129T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276094 | ||||||
| chr16:24276227
|
G | A | 10 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0137others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+19262G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276227 | ||||||
| chr16:24276254
|
C | T | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.211+19289C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276254 | ||||||
| chr16:24276335
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.211+19370G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276335 | ||||||
| chr16:24276371
|
A | G | 50 | a0001c0001t0001g0169a0001c0001t0001g0280a0001c0001t0001g0294others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+19406A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276371 | ||||||
| chr16:24276544
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+19579T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276544 | ||||||
| chr16:24276851
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211+19886G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276851 | ||||||
| chr16:24276893
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+19928T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276893 | ||||||
| chr16:24276904
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+19939T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24276904 | ||||||
| chr16:24277191
|
T | C | 11 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0137others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+20226T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277191 | ||||||
| chr16:24277266
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211+20301C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277266 | ||||||
| chr16:24277301
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.211+20336G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277301 | ||||||
| chr16:24277306
|
G | C | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+20341G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277306 | ||||||
| chr16:24277374
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+20409G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277374 | ||||||
| chr16:24277407
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0183 | 2 | HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.211+20442C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277407 | ||||||
| chr16:24277418
|
C | G | 50 | a0001c0001t0001g0169a0001c0001t0001g0280a0001c0001t0001g0294others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+20453C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277418 | ||||||
| chr16:24277431
|
C | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(243): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.211+20466C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277431 | ||||||
| chr16:24277541
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+20576G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277541 | ||||||
| chr16:24277547
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+20582C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277547 | ||||||
| chr16:24277548
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.211+20583G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277548 | ||||||
| chr16:24277561
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0166 | 2 | HG00408.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.211+20596G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277561 | ||||||
| chr16:24277601
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.211+20636C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24277601 | ||||||
| chr16:24277779
|
C | CA | 84 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.211+20832dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24277779 | |||||
| chr16:24277779
|
CA | C | 86 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.211+20832delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24277779 | |||||
| chr16:24278360
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+21395G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24278360 | ||||||
| chr16:24278663
|
G | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+21698G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24278663 | ||||||
| chr16:24278721
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0177 | 3 | HG02572.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.211+21756C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24278721 | ||||||
| chr16:24278725
|
C | G | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+21760C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24278725 | ||||||
| chr16:24278887
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.211+21922G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24278887 | ||||||
| chr16:24279336
|
C | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.211+22371C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279336 | ||||||
| chr16:24279343
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+22378G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279343 | ||||||
| chr16:24279641
|
C | T | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.211+22676C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279641 | ||||||
| chr16:24279732
|
T | A | 136 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.211+22767T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279732 | ||||||
| chr16:24279758
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.211+22793G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279758 | ||||||
| chr16:24279926
|
G | C | 3 | a0001c0001t0001g0073a0001c0001t0002g0072a0001c0001t0002g0171 | 3 | HG02735.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.211+22961G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279926 | ||||||
| chr16:24279993
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.211+23028G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24279993 | ||||||
| chr16:24280098
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0365 | 2 | HG01934.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.211+23133T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280098 | ||||||
| chr16:24280171
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.211+23206T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280171 | ||||||
| chr16:24280177
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.211+23212C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280177 | ||||||
| chr16:24280202
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.211+23237G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280202 | ||||||
| chr16:24280401
|
C | T | 5 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0001g0344others(2): Show | 5 | NA18946.hp2 NA18968.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+23436C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280401 | ||||||
| chr16:24280424
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0194 | 2 | HG02559.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.211+23459C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280424 | ||||||
| chr16:24280603
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.211+23638G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280603 | ||||||
| chr16:24280669
|
A | C | 1 | a0001c0001t0001g0360 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.211+23704A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280669 | ||||||
| chr16:24280670
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(88): Show | 91 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.211+23705G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280670 | ||||||
| chr16:24280821
|
C | CA | 15 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0074others(12): Show | 15 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+23880dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAA | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+23879_211+2388 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAA | 44 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0280others(41): Show | 44 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+23876_211+2388 others(9): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAAA | 16 | a0001c0001t0001g0126a0001c0001t0001g0205a0001c0001t0001g0222others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.211+23875_211+2388 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAAAA | 49 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025others(46): Show | 49 | HG00323.hp1 HG02015.hp2 HG02040.hp2 others(46): Show |
intron_variant | MODIFIER | c.211+23874_211+2388 others(11): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAAAA others(1): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(27): Show | 30 | HG00423.hp1 HG00673.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.211+23873_211+2388 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0067 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.211+23871_211+2388 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+23868_211+2388 others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280821
|
CA | C | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.211+23880delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280821 | |||||
| chr16:24280866
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.211+23901A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280866 | ||||||
| chr16:24280896
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.211+23931A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24280896 | ||||||
| chr16:24280986
|
CAGAA | C | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.211+24025_211+2402 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24280986 | |||||
| chr16:24281134
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0183 | 2 | HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.211+24169G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281134 | ||||||
| chr16:24281356
|
C | G | 1 | a0001c0001t0001g0303 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.211+24391C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281356 | ||||||
| chr16:24281374
|
C | CT | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.211+24420dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24281374 | |||||
| chr16:24281517
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.211+24552G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281517 | ||||||
| chr16:24281640
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+24675C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281640 | ||||||
| chr16:24281964
|
A | C | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.211+24999A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281964 | ||||||
| chr16:24281977
|
A | G | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+25012A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24281977 | ||||||
| chr16:24282142
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.211+25177G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282142 | ||||||
| chr16:24282187
|
T | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.211+25222T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282187 | ||||||
| chr16:24282273
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.211+25308A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282273 | ||||||
| chr16:24282331
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.211+25366A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282331 | ||||||
| chr16:24282406
|
C | CT | 106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.211+25454dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24282406 | |||||
| chr16:24282406
|
CT | C | 9 | a0001c0001t0001g0098a0001c0001t0001g0147a0001c0001t0001g0151others(6): Show | 9 | HG01106.hp1 HG01943.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+25454delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24282406 | |||||
| chr16:24282424
|
G | T | 11 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0137others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+25459G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282424 | ||||||
| chr16:24282593
|
T | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0200 | 2 | NA18942.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.211+25628T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282593 | ||||||
| chr16:24282609
|
A | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0351 | 2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.211+25644A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282609 | ||||||
| chr16:24282786
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.211+25821C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282786 | ||||||
| chr16:24282789
|
C | G | 120 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(117): Show | 120 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.211+25824C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24282789 | ||||||
| chr16:24283045
|
T | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0295 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.211+26080T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283045 | ||||||
| chr16:24283050
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.211+26085A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283050 | ||||||
| chr16:24283094
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+26129G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283094 | ||||||
| chr16:24283094
|
G | C | 10 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0137others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+26129G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283094 | ||||||
| chr16:24283100
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0158 | 3 | HG00733.hp1 HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.211+26135C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283100 | ||||||
| chr16:24283127
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.211+26162T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283127 | ||||||
| chr16:24283256
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.211+26291T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283256 | ||||||
| chr16:24283322
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.211+26357C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283322 | ||||||
| chr16:24283425
|
T | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0315 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.211+26460T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283425 | ||||||
| chr16:24283778
|
C | G | 211 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(208): Show | 211 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.211+26813C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283778 | ||||||
| chr16:24283833
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+26868C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283833 | ||||||
| chr16:24283923
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+26958C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283923 | ||||||
| chr16:24283998
|
T | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0041others(36): Show | 39 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.211+27033T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24283998 | ||||||
| chr16:24284195
|
A | C | 211 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(208): Show | 211 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.211+27230A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284195 | ||||||
| chr16:24284212
|
G | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0109others(1): Show | 4 | HG01258.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+27247G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284212 | ||||||
| chr16:24284339
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0258 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.211+27374G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284339 | ||||||
| chr16:24284368
|
T | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.211+27403T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284368 | ||||||
| chr16:24284432
|
A | G | 2 | a0001c0001t0001g0340a0001c0001t0001g0345 | 2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.211+27467A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284432 | ||||||
| chr16:24284665
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.211+27700A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284665 | ||||||
| chr16:24284862
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+27897G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284862 | ||||||
| chr16:24284863
|
C | A | 1 | a0001c0001t0002g0283 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.211+27898C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284863 | ||||||
| chr16:24284878
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.211+27913C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284878 | ||||||
| chr16:24284883
|
CAA | C | 117 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.211+27919_211+2792 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284883 | ||||||
| chr16:24284931
|
G | C | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+27966G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284931 | ||||||
| chr16:24284955
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.211+27990T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24284955 | ||||||
| chr16:24285013
|
CA | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0091a0001c0001t0001g0106others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+28064delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24285013 | |||||
| chr16:24285267
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+28302A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285267 | ||||||
| chr16:24285365
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.211+28400G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285365 | ||||||
| chr16:24285451
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+28486C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285451 | ||||||
| chr16:24285490
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0223a0001c0001t0002g0251 | 3 | HG02109.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.211+28525C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285490 | ||||||
| chr16:24285556
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.211+28591A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285556 | ||||||
| chr16:24285610
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211+28645G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285610 | ||||||
| chr16:24285666
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.211+28701A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285666 | ||||||
| chr16:24285704
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.211+28739T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285704 | ||||||
| chr16:24285845
|
C | CT | 18 | a0001c0001t0001g0042a0001c0001t0001g0099a0001c0001t0001g0126others(15): Show | 18 | HG00280.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.211+28896dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24285845 | |||||
| chr16:24285845
|
C | CTT | 191 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(188): Show | 191 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.211+28895_211+2889 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24285845 | |||||
| chr16:24285905
|
G | A | 38 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0041others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.211+28940G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285905 | ||||||
| chr16:24285920
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+28955T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285920 | ||||||
| chr16:24285970
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+29005G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24285970 | ||||||
| chr16:24286072
|
G | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+29107G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286072 | ||||||
| chr16:24286149
|
A | G | 79 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.211+29184A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286149 | ||||||
| chr16:24286200
|
C | A | 117 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.211+29235C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286200 | ||||||
| chr16:24286361
|
G | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0041others(37): Show | 40 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.211+29396G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286361 | ||||||
| chr16:24286365
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.211+29400G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286365 | ||||||
| chr16:24286407
|
GAC | G | 214 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(211): Show | 214 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.211+29468_211+2946 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24286407 | |||||
| chr16:24286431
|
CACAT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0169others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.211+29468_211+2947 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24286431 | |||||
| chr16:24286433
|
CAT | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0306a0001c0001t0001g0359 | 3 | HG00642.hp1 HG01884.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.211+29479_211+2948 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24286433 | |||||
| chr16:24286435
|
T | C | 2 | a0001c0001t0001g0285a0001c0001t0002g0286 | 2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.211+29470T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286435 | ||||||
| chr16:24286538
|
C | T | 1 | a0001c0001t0001g0365 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211+29573C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286538 | ||||||
| chr16:24286650
|
G | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+29685G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286650 | ||||||
| chr16:24286662
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+29697C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286662 | ||||||
| chr16:24286664
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+29699T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286664 | ||||||
| chr16:24286905
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+29940G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24286905 | ||||||
| chr16:24287028
|
A | G | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+30063A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287028 | ||||||
| chr16:24287150
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0042 | 2 | HG02071.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.211+30185A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287150 | ||||||
| chr16:24287211
|
C | T | 209 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(206): Show | 209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+30246C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287211 | ||||||
| chr16:24287321
|
C | A | 4 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0001g0348others(1): Show | 4 | HG00673.hp1 HG02165.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+30356C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287321 | ||||||
| chr16:24287356
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0268 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.211+30391A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287356 | ||||||
| chr16:24287450
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0002g0002 | 2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.211+30485G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287450 | ||||||
| chr16:24287475
|
G | C | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+30510G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287475 | ||||||
| chr16:24287494
|
G | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0167others(5): Show | 8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+30529G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287494 | ||||||
| chr16:24287514
|
C | CA | 18 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0063others(15): Show | 18 | HG00642.hp2 HG01256.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+30569dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24287514 | |||||
| chr16:24287556
|
T | A | 1 | a0001c0001t0002g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+30591T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24287556 | ||||||
| chr16:24288100
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+31135C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288100 | ||||||
| chr16:24288111
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+31146C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288111 | ||||||
| chr16:24288147
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+31182T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288147 | ||||||
| chr16:24288234
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+31269G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288234 | ||||||
| chr16:24288245
|
T | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.211+31280T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288245 | ||||||
| chr16:24288285
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211+31320C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288285 | ||||||
| chr16:24288314
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+31349C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288314 | ||||||
| chr16:24288350
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0280others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+31385T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288350 | ||||||
| chr16:24288423
|
G | T | 2 | a0001c0001t0001g0318a0001c0001t0002g0325 | 2 | HG00140.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.211+31458G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288423 | ||||||
| chr16:24288440
|
G | T | 1 | a0001c0001t0001g0281 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.211+31475G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288440 | ||||||
| chr16:24288479
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+31514C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288479 | ||||||
| chr16:24288625
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+31660A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288625 | ||||||
| chr16:24288872
|
A | AAC | 24 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0142others(21): Show | 24 | HG00280.hp2 HG00423.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.211+31930_211+3193 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24288872 | |||||
| chr16:24288873
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.211+31908A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288873 | ||||||
| chr16:24288966
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0280others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+32001G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24288966 | ||||||
| chr16:24289031
|
C | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+32066C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24289031 | ||||||
| chr16:24289152
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0130 | 2 | NA18953.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.211+32187G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24289152 | ||||||
| chr16:24289311
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+32346A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24289311 | ||||||
| chr16:24289319
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.211+32354A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24289319 | ||||||
| chr16:24289844
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.211+32879G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24289844 | ||||||
| chr16:24290109
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.211+33144A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290109 | ||||||
| chr16:24290154
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+33189G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290154 | ||||||
| chr16:24290348
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.211+33383C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290348 | ||||||
| chr16:24290361
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211+33396G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290361 | ||||||
| chr16:24290380
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+33415C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290380 | ||||||
| chr16:24290410
|
C | T | 46 | a0001c0001t0001g0169a0001c0001t0001g0280a0001c0001t0001g0294others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.211+33445C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290410 | ||||||
| chr16:24290433
|
A | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.211+33468A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290433 | ||||||
| chr16:24290576
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+33611T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290576 | ||||||
| chr16:24290620
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.211+33655A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290620 | ||||||
| chr16:24290692
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0156others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+33727G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290692 | ||||||
| chr16:24290708
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.211+33743G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290708 | ||||||
| chr16:24290717
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.211+33752G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290717 | ||||||
| chr16:24290971
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+34006A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24290971 | ||||||
| chr16:24291126
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(78): Show | 81 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.211+34161T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24291126 | ||||||
| chr16:24291221
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.211+34256C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24291221 | ||||||
| chr16:24291406
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0158 | 3 | HG00733.hp1 HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.211+34441A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24291406 | ||||||
| chr16:24291467
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.211+34502A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24291467 | ||||||
| chr16:24291514
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0167others(5): Show | 8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+34549G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24291514 | ||||||
| chr16:24292012
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0339 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.211+35047G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292012 | ||||||
| chr16:24292162
|
C | T | 1 | a0001c0001t0002g0352 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.211+35197C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292162 | ||||||
| chr16:24292209
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.211+35244A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292209 | ||||||
| chr16:24292253
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0194others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.211+35288C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292253 | ||||||
| chr16:24292254
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0166 | 2 | HG00408.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.211+35289G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292254 | ||||||
| chr16:24292565
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0360a0001c0001t0001g0362 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.211+35600T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292565 | ||||||
| chr16:24292744
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211+35779G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292744 | ||||||
| chr16:24292894
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.211+35929G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24292894 | ||||||
| chr16:24293017
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.211+36052A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293017 | ||||||
| chr16:24293030
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0345 | 2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.211+36065C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293030 | ||||||
| chr16:24293123
|
G | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(77): Show | 80 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.211+36158G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293123 | ||||||
| chr16:24293346
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.211+36381G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293346 | ||||||
| chr16:24293393
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.211+36428A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293393 | ||||||
| chr16:24293505
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0002g0067 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.211+36540C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293505 | ||||||
| chr16:24293510
|
A | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0025others(30): Show | 33 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.211+36545A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293510 | ||||||
| chr16:24293659
|
A | C | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.211+36694A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293659 | ||||||
| chr16:24293673
|
C | T | 1 | a0001c0001t0004g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.211+36708C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293673 | ||||||
| chr16:24293917
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+36952C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24293917 | ||||||
| chr16:24294109
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0280others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+37144G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294109 | ||||||
| chr16:24294231
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+37266G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294231 | ||||||
| chr16:24294518
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211+37553A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294518 | ||||||
| chr16:24294757
|
G | T | 3 | a0001c0001t0001g0304a0001c0001t0001g0336a0001c0001t0001g0347 | 3 | HG00639.hp1 HG01074.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.211+37792G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294757 | ||||||
| chr16:24294784
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.211+37819G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294784 | ||||||
| chr16:24294839
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.211+37874C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294839 | ||||||
| chr16:24294849
|
A | G | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.211+37884A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294849 | ||||||
| chr16:24294852
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+37887G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294852 | ||||||
| chr16:24294874
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(293): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.211+37909G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24294874 | ||||||
| chr16:24295230
|
C | A | 297 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(294): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.211+38265C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295230 | ||||||
| chr16:24295274
|
A | G | 59 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0049others(56): Show | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.211+38309A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295274 | ||||||
| chr16:24295382
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.211+38417C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295382 | ||||||
| chr16:24295583
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+38618A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295583 | ||||||
| chr16:24295749
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.211+38784T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295749 | ||||||
| chr16:24295839
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.211+38874C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295839 | ||||||
| chr16:24295982
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0158others(1): Show | 4 | HG00733.hp1 HG02698.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+39017T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24295982 | ||||||
| chr16:24296055
|
G | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0091others(40): Show | 43 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.211+39090G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296055 | ||||||
| chr16:24296075
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.211+39110A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296075 | ||||||
| chr16:24296277
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0148a0001c0001t0002g0132 | 3 | NA18950.hp2 NA18965.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.211+39312T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296277 | ||||||
| chr16:24296469
|
C | T | 41 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0091others(38): Show | 41 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.211+39504C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296469 | ||||||
| chr16:24296536
|
TG | T | 98 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.211+39574delG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24296536 | |||||
| chr16:24296648
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.211+39683T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296648 | ||||||
| chr16:24296733
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.211+39768C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296733 | ||||||
| chr16:24296936
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.211+39971T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24296936 | ||||||
| chr16:24297004
|
C | T | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+40039C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297004 | ||||||
| chr16:24297132
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.211+40167G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297132 | ||||||
| chr16:24297234
|
CAGAATCC others(27): Show |
C | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+40270_211+4030 others(38): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297234 | ||||||
| chr16:24297249
|
A | AAAAAT | 18 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(15): Show | 18 | HG01175.hp2 HG01496.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+40313_211+4031 others(9): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297249 | |||||
| chr16:24297271
|
A | G | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+40306A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297271 | ||||||
| chr16:24297275
|
A | AAAAT | 5 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0114others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+40334_211+4033 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297275 | |||||
| chr16:24297278
|
A | T | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+40313A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297278 | ||||||
| chr16:24297279
|
T | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+40314T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297279 | ||||||
| chr16:24297383
|
G | A | 71 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0028others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.211+40418G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297383 | ||||||
| chr16:24297504
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.211+40539C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297504 | ||||||
| chr16:24297605
|
G | C | 1 | a0001c0001t0001g0346 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.211+40640G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297605 | ||||||
| chr16:24297719
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211+40754A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297719 | ||||||
| chr16:24297761
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.211+40796C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297761 | ||||||
| chr16:24297787
|
T | C | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(90): Show | 93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.211+40822T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297787 | ||||||
| chr16:24297814
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0311 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.211+40849C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297814 | ||||||
| chr16:24297956
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.211+40991G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24297956 | ||||||
| chr16:24297987
|
C | CTG | 9 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0295others(6): Show | 9 | HG01496.hp2 HG02280.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+41056_211+4105 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297987 | |||||
| chr16:24297987
|
CTG | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.211+41056_211+4105 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297987 | |||||
| chr16:24297987
|
CTGTG | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0041others(33): Show | 36 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.211+41054_211+4105 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297987 | |||||
| chr16:24297987
|
CTGTGTG | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0195a0001c0001t0001g0284others(1): Show | 4 | HG01074.hp1 HG02647.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+41052_211+4105 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297987 | |||||
| chr16:24297987
|
CTGTGTGT others(1): Show |
C | 117 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.211+41050_211+4105 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24297987 | |||||
| chr16:24298002
|
T | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG00544.hp2 HG00558.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.211+41037T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298002 | ||||||
| chr16:24298145
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+41180C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298145 | ||||||
| chr16:24298289
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.211+41324T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298289 | ||||||
| chr16:24298342
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.211+41377T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298342 | ||||||
| chr16:24298586
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+41621G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298586 | ||||||
| chr16:24298635
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.211+41670C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298635 | ||||||
| chr16:24298668
|
T | C | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0016others(68): Show | 71 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.211+41703T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298668 | ||||||
| chr16:24298779
|
A | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0019others(24): Show | 27 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.211+41814A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298779 | ||||||
| chr16:24298894
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.211+41929T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298894 | ||||||
| chr16:24298961
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.211+41996A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24298961 | ||||||
| chr16:24299049
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0322 | 2 | HG01934.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.211+42084T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299049 | ||||||
| chr16:24299177
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.211+42212G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299177 | ||||||
| chr16:24299181
|
T | C | 365 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.211+42216T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299181 | ||||||
| chr16:24299223
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+42258C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299223 | ||||||
| chr16:24299288
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.211+42323A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299288 | ||||||
| chr16:24299536
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+42571G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299536 | ||||||
| chr16:24299561
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.211+42596G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299561 | ||||||
| chr16:24299611
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.211+42646C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299611 | ||||||
| chr16:24299938
|
G | GCA | 49 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0021others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.211+42994_211+4299 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24299938 | |||||
| chr16:24299942
|
A | G | 3 | a0001c0001t0001g0299a0001c0001t0001g0355a0001c0001t0003g0202 | 3 | HG01243.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.211+42977A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299942 | ||||||
| chr16:24299961
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.211+42996T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299961 | ||||||
| chr16:24299963
|
C | T | 4 | a0001c0001t0001g0287a0001c0001t0002g0310a0001c0001t0002g0312others(1): Show | 4 | HG03098.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+42998C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24299963 | ||||||
| chr16:24300053
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.211+43088A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300053 | ||||||
| chr16:24300082
|
A | G | 3 | a0001c0001t0001g0299a0001c0001t0001g0355a0001c0001t0003g0202 | 3 | HG01243.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.211+43117A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300082 | ||||||
| chr16:24300256
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0121 | 2 | HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.211+43291G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300256 | ||||||
| chr16:24300308
|
G | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.211+43343G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300308 | ||||||
| chr16:24300312
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211+43347C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300312 | ||||||
| chr16:24300363
|
G | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.211+43398G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300363 | ||||||
| chr16:24300390
|
G | T | 12 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0135others(9): Show | 12 | HG02027.hp1 HG02155.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+43425G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300390 | ||||||
| chr16:24300419
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.211+43454T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300419 | ||||||
| chr16:24300601
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+43636A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300601 | ||||||
| chr16:24300620
|
C | CA | 26 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0057others(23): Show | 26 | HG01256.hp2 HG02027.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+43670dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24300620 | |||||
| chr16:24300620
|
CA | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(95): Show | 98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.211+43670delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24300620 | |||||
| chr16:24300630
|
A | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0234 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.211+43665A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300630 | ||||||
| chr16:24300666
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.211+43701T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300666 | ||||||
| chr16:24300745
|
G | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.211+43780G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300745 | ||||||
| chr16:24300847
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.211+43882T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300847 | ||||||
| chr16:24300855
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0100others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+43890C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300855 | ||||||
| chr16:24300887
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.211+43922A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300887 | ||||||
| chr16:24300905
|
C | T | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+43940C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300905 | ||||||
| chr16:24300987
|
G | A | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+44022G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24300987 | ||||||
| chr16:24301043
|
C | CA | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(139): Show | 142 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.211+44096dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24301043 | |||||
| chr16:24301043
|
C | CAA | 10 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0159others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+44095_211+4409 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24301043 | |||||
| chr16:24301146
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+44181G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301146 | ||||||
| chr16:24301206
|
G | GA | 11 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0091others(8): Show | 11 | HG00673.hp1 HG01361.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+44257dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24301206 | |||||
| chr16:24301206
|
GA | G | 34 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0074others(31): Show | 34 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.211+44257delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24301206 | |||||
| chr16:24301224
|
C | A | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+44259C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301224 | ||||||
| chr16:24301300
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+44335G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301300 | ||||||
| chr16:24301363
|
G | C | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+44398G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301363 | ||||||
| chr16:24301407
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.211+44442T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301407 | ||||||
| chr16:24301447
|
T | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 121 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.211+44482T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301447 | ||||||
| chr16:24301480
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0315 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.211+44515C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301480 | ||||||
| chr16:24301518
|
G | T | 7 | a0001c0001t0001g0160a0001c0001t0001g0242a0001c0001t0001g0243others(4): Show | 7 | HG00423.hp1 HG00558.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+44553G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301518 | ||||||
| chr16:24301605
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211+44640T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301605 | ||||||
| chr16:24301773
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.211+44808C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24301773 | ||||||
| chr16:24302075
|
G | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.212-44659G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24302075 | ||||||
| chr16:24302157
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.212-44577C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24302157 | ||||||
| chr16:24302331
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-44403C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24302331 | ||||||
| chr16:24302332
|
A | G | 96 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.212-44402A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24302332 | ||||||
| chr16:24302635
|
T | TTTTTG | 16 | a0001c0001t0001g0037a0001c0001t0001g0080a0001c0001t0001g0115others(13): Show | 16 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-44061_212-4405 others(9): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24302635 | |||||
| chr16:24302635
|
TTTTTG | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.212-44061_212-4405 others(9): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24302635 | |||||
| chr16:24302635
|
TTTTTGTT others(3): Show |
T | 36 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0035others(33): Show | 36 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.212-44066_212-4405 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24302635 | |||||
| chr16:24302635
|
TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-44071_212-4405 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24302635 | |||||
| chr16:24302777
|
A | C | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.212-43957A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24302777 | ||||||
| chr16:24303206
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0080others(32): Show | 35 | HG00544.hp1 HG01106.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.212-43528G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24303206 | ||||||
| chr16:24303284
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-43450C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24303284 | ||||||
| chr16:24303344
|
G | GTATT | 67 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(64): Show | 67 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.212-43367_212-4336 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24303344 | |||||
| chr16:24303344
|
G | GTATTTAT others(1): Show |
3 | a0001c0001t0001g0122a0001c0001t0002g0308a0001c0001t0004g0331 | 3 | HG02258.hp1 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.212-43371_212-4336 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24303344 | |||||
| chr16:24303344
|
G | GTATTTAT others(5): Show |
1 | a0001c0001t0001g0012 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.212-43375_212-4336 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24303344 | |||||
| chr16:24303401
|
G | C | 1 | a0001c0001t0001g0351 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.212-43333G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24303401 | ||||||
| chr16:24303548
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0002g0002a0001c0002t0001g0190 | 3 | HG00280.hp2 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.212-43186C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24303548 | ||||||
| chr16:24303633
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0247 | 2 | HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.212-43101G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24303633 | ||||||
| chr16:24304070
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-42664C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304070 | ||||||
| chr16:24304103
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.212-42631C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304103 | ||||||
| chr16:24304215
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-42519C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304215 | ||||||
| chr16:24304243
|
G | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.212-42491G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304243 | ||||||
| chr16:24304326
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0183 | 2 | HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.212-42408C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304326 | ||||||
| chr16:24304376
|
G | C | 6 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0178others(3): Show | 6 | HG00323.hp2 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-42358G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304376 | ||||||
| chr16:24304457
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0241 | 3 | HG03654.hp1 NA18946.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.212-42277G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304457 | ||||||
| chr16:24304538
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG03041.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-42196C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304538 | ||||||
| chr16:24304539
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0287 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-42195G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304539 | ||||||
| chr16:24304710
|
G | A | 2 | a0001c0001t0001g0013a0001c0003t0001g0237 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.212-42024G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24304710 | ||||||
| chr16:24305143
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.212-41591C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305143 | ||||||
| chr16:24305144
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.212-41590C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305144 | ||||||
| chr16:24305145
|
G | A | 1 | a0001c0001t0004g0334 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.212-41589G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305145 | ||||||
| chr16:24305149
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0039others(8): Show | 11 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-41585G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305149 | ||||||
| chr16:24305188
|
G | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0223others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-41546G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305188 | ||||||
| chr16:24305292
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.212-41442A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305292 | ||||||
| chr16:24305308
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-41426A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305308 | ||||||
| chr16:24305320
|
A | ATG | 81 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0027others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.212-41368_212-4136 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
A | ATGTG | 18 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0051others(15): Show | 18 | HG00673.hp2 HG01433.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-41370_212-4136 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATG | A | 82 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0024others(79): Show | 82 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.212-41368_212-4136 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTG | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0055others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-41370_212-4136 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTG | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(54): Show | 57 | HG00544.hp1 HG01358.hp1 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.212-41372_212-4136 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTGT others(1): Show |
A | 3 | a0001c0001t0001g0169a0001c0001t0001g0240a0001c0001t0001g0266 | 3 | HG02155.hp2 NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.212-41374_212-4136 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0292others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-41376_212-4136 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTGT others(7): Show |
A | 15 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0167others(12): Show | 15 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.212-41380_212-4136 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTGT others(9): Show |
A | 30 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(27): Show | 30 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-41382_212-4136 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305320
|
ATGTGTGT others(11): Show |
A | 15 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0079others(12): Show | 15 | HG00140.hp1 HG00741.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-41384_212-4136 others(22): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24305320 | |||||
| chr16:24305338
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.212-41396G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305338 | ||||||
| chr16:24305348
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-41386G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305348 | ||||||
| chr16:24305578
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.212-41156T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305578 | ||||||
| chr16:24305628
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-41106A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305628 | ||||||
| chr16:24305743
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0004g0331 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.212-40991C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305743 | ||||||
| chr16:24305864
|
T | G | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-40870T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305864 | ||||||
| chr16:24305926
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0119a0001c0001t0001g0302others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-40808G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24305926 | ||||||
| chr16:24306001
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.212-40733G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306001 | ||||||
| chr16:24306052
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.212-40682G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306052 | ||||||
| chr16:24306099
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.212-40635C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306099 | ||||||
| chr16:24306200
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0002g0002a0001c0001t0002g0283others(1): Show | 4 | HG00280.hp2 HG01175.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-40534G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306200 | ||||||
| chr16:24306255
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0291 | 2 | HG02615.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.212-40479G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306255 | ||||||
| chr16:24306333
|
A | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0035others(23): Show | 26 | HG01496.hp2 HG01891.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.212-40401A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306333 | ||||||
| chr16:24306433
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0088others(9): Show | 12 | HG02647.hp1 HG02647.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-40301C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306433 | ||||||
| chr16:24306454
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0004g0331 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.212-40280C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306454 | ||||||
| chr16:24306524
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-40210T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306524 | ||||||
| chr16:24306535
|
C | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.212-40199C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306535 | ||||||
| chr16:24306692
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0322 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-40042T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306692 | ||||||
| chr16:24306793
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-39941C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306793 | ||||||
| chr16:24306863
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0100others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-39871C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306863 | ||||||
| chr16:24306946
|
G | A | 2 | a0001c0001t0001g0013a0001c0003t0001g0237 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.212-39788G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306946 | ||||||
| chr16:24306967
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0002g0308 | 2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.212-39767A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306967 | ||||||
| chr16:24306981
|
T | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.212-39753T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306981 | ||||||
| chr16:24306999
|
G | C | 1 | a0001c0001t0001g0261 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.212-39735G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24306999 | ||||||
| chr16:24307356
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.212-39378A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307356 | ||||||
| chr16:24307359
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-39375T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307359 | ||||||
| chr16:24307431
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.212-39303C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307431 | ||||||
| chr16:24307472
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0322 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-39262T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307472 | ||||||
| chr16:24307635
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.212-39099A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307635 | ||||||
| chr16:24307849
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.212-38885C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307849 | ||||||
| chr16:24307931
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-38803T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307931 | ||||||
| chr16:24307939
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0322 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-38795C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307939 | ||||||
| chr16:24307978
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0004g0331 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.212-38756T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307978 | ||||||
| chr16:24307991
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-38743G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24307991 | ||||||
| chr16:24308047
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.212-38687C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308047 | ||||||
| chr16:24308101
|
A | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-38633A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308101 | ||||||
| chr16:24308104
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-38630G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308104 | ||||||
| chr16:24308106
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-38628A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308106 | ||||||
| chr16:24308236
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-38498T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308236 | ||||||
| chr16:24308313
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.212-38421T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308313 | ||||||
| chr16:24308347
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-38387C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308347 | ||||||
| chr16:24308373
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.212-38361T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308373 | ||||||
| chr16:24308475
|
G | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(39): Show | 42 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.212-38259G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308475 | ||||||
| chr16:24308478
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.212-38256C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308478 | ||||||
| chr16:24308614
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0100others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-38120G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308614 | ||||||
| chr16:24308705
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-38029C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308705 | ||||||
| chr16:24308804
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-37930T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308804 | ||||||
| chr16:24308839
|
C | CA | 36 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(33): Show | 36 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.212-37867dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24308839 | |||||
| chr16:24308839
|
CA | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0029others(64): Show | 67 | HG00544.hp1 HG00733.hp1 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.212-37867delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24308839 | |||||
| chr16:24308839
|
CAA | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0044others(53): Show | 56 | HG01106.hp1 HG01168.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.212-37868_212-3786 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24308839 | |||||
| chr16:24308839
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.212-37878_212-3786 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24308839 | |||||
| chr16:24308863
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.212-37871A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308863 | ||||||
| chr16:24308878
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0226a0001c0001t0006g0053 | 3 | HG00738.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.212-37856A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308878 | ||||||
| chr16:24308999
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.212-37735C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24308999 | ||||||
| chr16:24309066
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0287a0001c0001t0001g0322 | 3 | HG02818.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-37668A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309066 | ||||||
| chr16:24309119
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0014others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.212-37615A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309119 | ||||||
| chr16:24309123
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0322 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-37611T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309123 | ||||||
| chr16:24309124
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-37610T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309124 | ||||||
| chr16:24309238
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.212-37496A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309238 | ||||||
| chr16:24309429
|
A | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.212-37305A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309429 | ||||||
| chr16:24309445
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(113): Show | 116 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(113): Show |
intron_variant | MODIFIER | c.212-37289G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309445 | ||||||
| chr16:24309448
|
A | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0236a0001c0001t0001g0319 | 3 | HG02647.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212-37286A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309448 | ||||||
| chr16:24309470
|
C | G | 130 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0014others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.212-37264C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309470 | ||||||
| chr16:24309494
|
G | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0001g0087others(5): Show | 8 | HG01261.hp2 HG01496.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-37240G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309494 | ||||||
| chr16:24309520
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.212-37214T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309520 | ||||||
| chr16:24309620
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.212-37114G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309620 | ||||||
| chr16:24309645
|
A | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.212-37089A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309645 | ||||||
| chr16:24309796
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0186others(1): Show | 4 | HG01070.hp2 HG01943.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-36938C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309796 | ||||||
| chr16:24309816
|
A | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0324a0001c0001t0001g0358others(1): Show | 4 | NA18957.hp1 NA18962.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-36918A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309816 | ||||||
| chr16:24309866
|
G | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.212-36868G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309866 | ||||||
| chr16:24309948
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0322a0001c0001t0003g0224 | 3 | HG02818.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.212-36786T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309948 | ||||||
| chr16:24309949
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.212-36785A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24309949 | ||||||
| chr16:24310083
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0156others(11): Show | 14 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-36651G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310083 | ||||||
| chr16:24310116
|
G | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(72): Show | 75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.212-36618G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310116 | ||||||
| chr16:24310152
|
T | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0089a0001c0001t0001g0234others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-36582T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310152 | ||||||
| chr16:24310153
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.212-36581A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310153 | ||||||
| chr16:24310183
|
T | TG | 85 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(82): Show | 85 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.212-36549dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24310183 | |||||
| chr16:24310301
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.212-36433C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310301 | ||||||
| chr16:24310368
|
A | AG | 6 | a0001c0001t0001g0059a0001c0001t0001g0188a0001c0001t0001g0193others(3): Show | 6 | HG01934.hp2 HG02109.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-36365dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24310368 | |||||
| chr16:24310472
|
G | C | 1 | a0001c0001t0002g0320 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.212-36262G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310472 | ||||||
| chr16:24310481
|
T | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0032others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.212-36253T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310481 | ||||||
| chr16:24310565
|
A | AAAAC | 4 | a0001c0001t0001g0193a0001c0001t0001g0293a0001c0001t0004g0332others(1): Show | 4 | HG02109.hp1 HG03041.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-36152_212-3614 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24310565 | |||||
| chr16:24310565
|
A | AAAACAAA others(1): Show |
184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-36156_212-3614 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24310565 | |||||
| chr16:24310612
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.212-36122C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310612 | ||||||
| chr16:24310734
|
A | T | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-36000A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310734 | ||||||
| chr16:24310764
|
G | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(1): Show | 4 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-35970G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310764 | ||||||
| chr16:24310814
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.212-35920G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24310814 | ||||||
| chr16:24311046
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0032others(153): Show | 156 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.212-35688C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311046 | ||||||
| chr16:24311164
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-35570C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311164 | ||||||
| chr16:24311238
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0236a0001c0001t0004g0332 | 3 | HG00423.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.212-35496C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311238 | ||||||
| chr16:24311308
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(157): Show | 160 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.212-35426T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311308 | ||||||
| chr16:24311369
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0287a0001c0001t0001g0290others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-35365G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311369 | ||||||
| chr16:24311508
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(198): Show | 201 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.212-35213delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24311508 | |||||
| chr16:24311547
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.212-35187T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311547 | ||||||
| chr16:24311582
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.212-35152G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311582 | ||||||
| chr16:24311904
|
A | G | 1 | a0001c0001t0001g0353 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.212-34830A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311904 | ||||||
| chr16:24311909
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-34825C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24311909 | ||||||
| chr16:24312101
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.212-34633C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312101 | ||||||
| chr16:24312111
|
A | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-34623A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312111 | ||||||
| chr16:24312220
|
C | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0108others(1): Show | 4 | HG01109.hp2 HG01346.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-34514C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312220 | ||||||
| chr16:24312458
|
A | G | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-34276A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312458 | ||||||
| chr16:24312525
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.212-34209T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312525 | ||||||
| chr16:24312535
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0363 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-34199G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312535 | ||||||
| chr16:24312602
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-34132G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312602 | ||||||
| chr16:24312656
|
A | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-34078A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312656 | ||||||
| chr16:24312657
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.212-34077T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312657 | ||||||
| chr16:24312916
|
G | GAAGAAAG others(5): Show |
1 | a0001c0001t0001g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.212-33815_212-3381 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312916 | |||||
| chr16:24312916
|
G | GAAGAAAG others(9): Show |
1 | a0001c0001t0001g0270 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.212-33815_212-3381 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312916 | |||||
| chr16:24312920
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG03139.hp1 HG03471.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-33814G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312920 | ||||||
| chr16:24312920
|
G | GAAGA | 5 | a0001c0001t0001g0186a0001c0001t0001g0267a0001c0001t0001g0282others(2): Show | 5 | HG01943.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-33781_212-3377 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAAG others(1): Show |
10 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0085others(7): Show | 10 | HG00408.hp2 HG00423.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-33785_212-3377 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAAG others(5): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0031others(6): Show | 9 | HG01884.hp2 HG01978.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-33789_212-3377 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAAG others(9): Show |
14 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0180others(11): Show | 14 | HG02486.hp1 HG02717.hp2 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-33793_212-3377 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAAG others(13): Show |
5 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0208others(2): Show | 5 | HG02970.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-33797_212-3377 others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAAG others(17): Show |
2 | a0001c0001t0001g0266a0001c0001t0002g0002 | 2 | HG00280.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.212-33801_212-3377 others(28): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGAAGA others(8): Show |
2 | a0001c0001t0001g0339a0001c0001t0002g0342 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.212-33809_212-3380 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGGAAG others(5): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.212-33811_212-3381 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
G | GAAGGAAG others(9): Show |
4 | a0001c0001t0001g0322a0001c0001t0002g0310a0001c0001t0002g0312others(1): Show | 4 | HG02818.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-33811_212-3381 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312920
|
GAAGA | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0020others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.212-33781_212-3377 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312920 | |||||
| chr16:24312924
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-33810A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312924 | ||||||
| chr16:24312947
|
GAA | G | 56 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0038others(53): Show | 56 | HG00558.hp2 HG00673.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.212-33785_212-3378 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312947 | |||||
| chr16:24312952
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0062 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.212-33778_212-3377 others(15): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312952 | |||||
| chr16:24312953
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0117others(3): Show | 6 | HG02056.hp1 HG02280.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-33781A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312953 | ||||||
| chr16:24312953
|
AAG | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0038others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-33777_212-3377 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312953 | |||||
| chr16:24312955
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0117others(3): Show | 6 | HG02056.hp1 HG02280.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-33779G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312955 | ||||||
| chr16:24312955
|
G | GAA | 3 | a0001c0001t0001g0200a0001c0001t0001g0212a0001c0001t0002g0005 | 3 | NA18944.hp2 NA18956.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.212-33778_212-3377 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAA | 19 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(16): Show | 19 | HG01109.hp1 HG02027.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(3): Show |
21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(7): Show |
14 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0063others(11): Show | 14 | HG01123.hp1 HG01346.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(11): Show |
9 | a0001c0001t0001g0019a0001c0001t0001g0058a0001c0001t0001g0083others(6): Show | 9 | HG00099.hp2 HG00544.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(22): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(15): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0209others(1): Show | 4 | HG00558.hp1 HG03516.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(26): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(23): Show |
1 | a0001c0001t0003g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.212-33778_212-3377 others(34): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(21): Show |
1 | a0001c0001t0001g0104 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.212-33778_212-3377 others(32): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(17): Show |
6 | a0001c0001t0001g0123a0001c0001t0001g0158a0001c0001t0001g0229others(3): Show | 6 | HG00733.hp1 HG02738.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(28): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(19): Show |
1 | a0001c0001t0001g0279 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.212-33778_212-3377 others(30): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(13): Show |
7 | a0001c0001t0001g0043a0001c0001t0001g0141a0001c0001t0001g0170others(4): Show | 7 | HG02015.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(9): Show |
27 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0001t0001g0073others(24): Show | 27 | HG01074.hp1 HG01123.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAAA others(5): Show |
23 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0033others(20): Show | 23 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAAAGAGA others(1): Show |
25 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.212-33778_212-3377 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312955
|
G | GAGAA | 3 | a0001c0001t0001g0116a0001c0001t0001g0333a0001c0001t0002g0068 | 3 | HG01891.hp2 HG02148.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.212-33769_212-3376 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312955 | |||||
| chr16:24312959
|
A | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.212-33775A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312959 | ||||||
| chr16:24312966
|
A | AGAGAAAG others(5): Show |
1 | a0001c0001t0002g0005 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.212-33768_212-3376 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312966 | ||||||
| chr16:24312969
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-33765A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312969 | ||||||
| chr16:24312970
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-33764G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312970 | ||||||
| chr16:24312982
|
T | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0306 | 2 | HG00642.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.212-33752T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312982 | ||||||
| chr16:24312983
|
A | AAAAG | 8 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0163others(5): Show | 8 | HG00323.hp2 HG01070.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-33731_212-3372 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312983 | |||||
| chr16:24312983
|
AAAAG | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-33731_212-3372 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24312983 | |||||
| chr16:24312986
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-33748A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312986 | ||||||
| chr16:24312987
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-33747G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24312987 | ||||||
| chr16:24313007
|
AAG | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0002g0310others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-33721_212-3372 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313007 | |||||
| chr16:24313073
|
G | GAGGA | 47 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0024others(44): Show | 47 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.212-33626_212-3362 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(1): Show |
71 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0019others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.212-33630_212-3362 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(5): Show |
55 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp2 HG00642.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.212-33634_212-3362 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(9): Show |
41 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.212-33638_212-3362 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(13): Show |
23 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0059others(20): Show | 23 | HG00733.hp2 HG00738.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.212-33642_212-3362 others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(17): Show |
13 | a0001c0001t0001g0055a0001c0001t0001g0098a0001c0001t0001g0124others(10): Show | 13 | HG01891.hp2 HG02027.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-33646_212-3362 others(28): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
G | GAGGAAGG others(21): Show |
2 | a0001c0001t0001g0209a0001c0001t0003g0224 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.212-33650_212-3362 others(32): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313073
|
GAGGA | G | 12 | a0001c0001t0001g0102a0001c0001t0001g0118a0001c0001t0001g0126others(9): Show | 12 | HG02896.hp2 HG03139.hp1 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-33626_212-3362 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24313073 | |||||
| chr16:24313232
|
T | C | 1 | a0001c0002t0001g0190 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.212-33502T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313232 | ||||||
| chr16:24313414
|
A | C | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-33320A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313414 | ||||||
| chr16:24313533
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212-33201G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313533 | ||||||
| chr16:24313571
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-33163A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313571 | ||||||
| chr16:24313611
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.212-33123G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313611 | ||||||
| chr16:24313735
|
T | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-32999T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313735 | ||||||
| chr16:24313784
|
G | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0038others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-32950G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313784 | ||||||
| chr16:24313893
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.212-32841C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24313893 | ||||||
| chr16:24314115
|
C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0287a0001c0001t0001g0290others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-32619C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314115 | ||||||
| chr16:24314331
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.212-32403C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314331 | ||||||
| chr16:24314420
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0199a0001c0001t0001g0212others(1): Show | 4 | HG03195.hp2 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-32314C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314420 | ||||||
| chr16:24314473
|
A | G | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-32261A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314473 | ||||||
| chr16:24314733
|
G | GCCT | 30 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0038others(27): Show | 30 | HG00558.hp2 HG01358.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-31965_212-3196 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCT | 36 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0075others(33): Show | 36 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.212-31968_212-3196 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(2): Show |
59 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 59 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-31971_212-3196 others(13): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(5): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0077a0001c0001t0001g0094others(5): Show | 8 | HG01175.hp1 HG02132.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-31974_212-3196 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(8): Show |
14 | a0001c0001t0001g0059a0001c0001t0001g0088a0001c0001t0001g0107others(11): Show | 14 | HG00733.hp2 HG01243.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-31977_212-3196 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(11): Show |
10 | a0001c0001t0001g0055a0001c0001t0001g0098a0001c0001t0001g0207others(7): Show | 10 | HG00673.hp1 HG02572.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-31980_212-3196 others(22): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(14): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0204others(1): Show | 4 | HG00738.hp2 NA18942.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-31983_212-3196 others(25): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(17): Show |
1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-31986_212-3196 others(28): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
G | GCCTCCTC others(26): Show |
1 | a0001c0001t0001g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.212-31995_212-3196 others(37): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314733
|
GCCTCCTC others(2): Show |
G | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.212-31971_212-3196 others(13): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24314733 | |||||
| chr16:24314759
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0167a0001c0001t0001g0188others(4): Show | 7 | HG01934.hp2 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-31975C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314759 | ||||||
| chr16:24314802
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.212-31932C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314802 | ||||||
| chr16:24314827
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.212-31907G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314827 | ||||||
| chr16:24314859
|
T | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.212-31875T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314859 | ||||||
| chr16:24314891
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.212-31843C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314891 | ||||||
| chr16:24314927
|
A | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(218): Show | 221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.212-31807A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314927 | ||||||
| chr16:24314937
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.212-31797C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24314937 | ||||||
| chr16:24315133
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-31601C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315133 | ||||||
| chr16:24315200
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-31534C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315200 | ||||||
| chr16:24315218
|
T | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.212-31516T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315218 | ||||||
| chr16:24315401
|
A | C | 29 | a0001c0001t0001g0055a0001c0001t0001g0088a0001c0001t0001g0098others(26): Show | 29 | HG00673.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-31333A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315401 | ||||||
| chr16:24315441
|
GCCTT | G | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-31279_212-3127 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24315441 | |||||
| chr16:24315519
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.212-31215T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315519 | ||||||
| chr16:24315608
|
CT | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0094a0001c0001t0001g0115others(4): Show | 7 | HG01175.hp1 HG01496.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-31123delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24315608 | |||||
| chr16:24315674
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.212-31060T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315674 | ||||||
| chr16:24315738
|
T | C | 124 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(121): Show | 124 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.212-30996T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315738 | ||||||
| chr16:24315801
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0363 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-30933G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315801 | ||||||
| chr16:24315813
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30921A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315813 | ||||||
| chr16:24315849
|
G | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.212-30885G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315849 | ||||||
| chr16:24315927
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30807G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24315927 | ||||||
| chr16:24316002
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30732C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316002 | ||||||
| chr16:24316206
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30528G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316206 | ||||||
| chr16:24316244
|
G | GCACAGCT others(309): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0225others(1): Show | 4 | HG01168.hp1 HG01168.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-30474_212-3047 others(320): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(309): Show |
1 | a0001c0001t0001g0220 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.212-30474_212-3047 others(320): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(310): Show |
1 | a0001c0001t0001g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.212-30474_212-3047 others(321): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(309): Show |
1 | a0001c0001t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.212-30474_212-3047 others(320): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(310): Show |
1 | a0001c0001t0001g0355 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.212-30474_212-3047 others(321): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(310): Show |
77 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(74): Show | 77 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.212-30474_212-3047 others(321): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316244
|
G | GCACAGCT others(311): Show |
10 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0139others(7): Show | 10 | HG00408.hp1 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-30474_212-3047 others(322): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316244 | |||||
| chr16:24316246
|
A | ACAGCTCT others(310): Show |
1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.212-30474_212-3047 others(321): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316246 | |||||
| chr16:24316286
|
C | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30448C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316286 | ||||||
| chr16:24316293
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-30441C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316293 | ||||||
| chr16:24316377
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0230 | 2 | NA19062.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.212-30357C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316377 | ||||||
| chr16:24316446
|
C | CTGTCTT | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-30285_212-3028 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24316446 | |||||
| chr16:24316649
|
C | T | 4 | a0001c0001t0001g0188a0001c0001t0001g0291a0001c0001t0001g0293others(1): Show | 4 | HG01934.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-30085C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316649 | ||||||
| chr16:24316979
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.212-29755C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24316979 | ||||||
| chr16:24317006
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-29728G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317006 | ||||||
| chr16:24317111
|
T | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-29623T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317111 | ||||||
| chr16:24317163
|
T | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0360 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.212-29571T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317163 | ||||||
| chr16:24317178
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-29556C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317178 | ||||||
| chr16:24317190
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-29544T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317190 | ||||||
| chr16:24317195
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-29539A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317195 | ||||||
| chr16:24317294
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.212-29440C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317294 | ||||||
| chr16:24317312
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-29422C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317312 | ||||||
| chr16:24317316
|
C | A | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-29418C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317316 | ||||||
| chr16:24317317
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0296 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.212-29417G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317317 | ||||||
| chr16:24317372
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0065others(3): Show | 6 | HG00558.hp2 HG02165.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-29362T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317372 | ||||||
| chr16:24317449
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-29285C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317449 | ||||||
| chr16:24317539
|
C | CA | 16 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(13): Show | 16 | HG00735.hp2 HG01361.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-29183dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317539 | |||||
| chr16:24317539
|
C | CAA | 36 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.212-29184_212-2918 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317539 | |||||
| chr16:24317549
|
AAAG | A | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-29182_212-2918 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317549 | |||||
| chr16:24317549
|
AAAGAAAA others(6): Show |
A | 1 | a0001c0001t0003g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.212-29182_212-2917 others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317549 | |||||
| chr16:24317552
|
GAAA | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0277a0001c0001t0001g0349 | 3 | HG00673.hp1 HG02895.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.212-29179_212-2917 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317552 | |||||
| chr16:24317552
|
GAAAAAGA others(94): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.212-29179_212-2907 others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317552 | |||||
| chr16:24317554
|
A | AAAAG | 12 | a0001c0001t0001g0033a0001c0001t0001g0148a0001c0001t0001g0167others(9): Show | 12 | HG00140.hp1 HG01175.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-29110_212-2910 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
A | AAAAGAAA others(1): Show |
12 | a0001c0001t0001g0100a0001c0001t0001g0121a0001c0001t0001g0131others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-29114_212-2910 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
A | AAAAGAAA others(5): Show |
3 | a0001c0001t0001g0103a0001c0001t0001g0149a0001c0001t0001g0200 | 3 | HG00558.hp1 HG02080.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.212-29118_212-2910 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
A | AG | 5 | a0001c0001t0001g0326a0001c0001t0001g0339a0001c0001t0002g0067others(2): Show | 5 | HG02523.hp2 HG03130.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-29180_212-2917 others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317554 | ||||||
| chr16:24317554
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-29180A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317554 | ||||||
| chr16:24317554
|
AAAAG | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0031others(12): Show | 15 | HG00099.hp2 HG00423.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-29110_212-2910 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
AAAAGAAA others(1): Show |
A | 15 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0049others(12): Show | 15 | HG00733.hp2 HG01106.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.212-29114_212-2910 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
AAAAGAAA others(5): Show |
A | 10 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0041others(7): Show | 10 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-29118_212-2910 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
AAAAGAAA others(9): Show |
A | 3 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0356 | 3 | HG00544.hp1 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.212-29122_212-2910 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317554
|
AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.212-29126_212-2910 others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317554 | |||||
| chr16:24317555
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.212-29179A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317555 | ||||||
| chr16:24317560
|
AAG | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02132.hp1 NA19012.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-29172_212-2917 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317560 | |||||
| chr16:24317568
|
A | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(16): Show | 19 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.212-29166A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317568 | ||||||
| chr16:24317570
|
GAAAGAAA others(71): Show |
G | 14 | a0001c0001t0001g0050a0001c0001t0001g0112a0001c0001t0001g0125others(11): Show | 14 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-29106_212-2902 others(82): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317570 | |||||
| chr16:24317574
|
GAAAGAAA others(67): Show |
G | 4 | a0001c0001t0001g0015a0001c0001t0001g0189a0001c0001t0001g0240others(1): Show | 4 | HG01884.hp2 HG02109.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-29106_212-2903 others(78): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317574 | |||||
| chr16:24317578
|
GAAAGAAA others(63): Show |
G | 4 | a0001c0001t0001g0040a0001c0001t0001g0065a0001c0001t0001g0193others(1): Show | 4 | NA18999.hp1 NA18999.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-29106_212-2903 others(74): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317578 | |||||
| chr16:24317582
|
G | GAAAGAAA others(6): Show |
1 | a0001c0001t0002g0005 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.212-29149_212-2913 others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317582 | |||||
| chr16:24317582
|
G | GAAAGAAA others(3): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0233 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.212-29144_212-2914 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317582 | |||||
| chr16:24317582
|
GAAAGAAA others(59): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.212-29106_212-2904 others(70): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317582 | |||||
| chr16:24317586
|
G | GAAAGAAA others(7): Show |
1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-29136_212-2913 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317586 | |||||
| chr16:24317586
|
G | GAAAGGA | 3 | a0001c0001t0001g0017a0001c0001t0001g0075a0001c0001t0001g0164 | 3 | HG01192.hp1 HG01261.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.212-29144_212-2914 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317586 | |||||
| chr16:24317586
|
GAAAGAAA others(55): Show |
G | 1 | a0001c0001t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.212-29106_212-2904 others(66): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317586 | |||||
| chr16:24317590
|
G | GGA | 13 | a0001c0001t0001g0052a0001c0001t0001g0074a0001c0001t0001g0076others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-29144_212-2914 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317590 | ||||||
| chr16:24317594
|
G | GGA | 5 | a0001c0001t0001g0087a0001c0001t0001g0117a0001c0001t0001g0151others(2): Show | 5 | HG01496.hp1 HG02040.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-29140_212-2913 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317594 | ||||||
| chr16:24317599
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA19012.hp1 NA19054.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.212-29135A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317599 | ||||||
| chr16:24317600
|
AAG | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA19012.hp1 NA19054.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.212-29132_212-2913 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317600 | |||||
| chr16:24317602
|
G | GAAAGAAA others(19): Show |
1 | a0001c0001t0001g0123 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.212-29108_212-2910 others(30): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317602 | |||||
| chr16:24317602
|
G | GAAAGAAA others(7): Show |
1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-29120_212-2911 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317602 | |||||
| chr16:24317606
|
GAAAGAAA others(100): Show |
G | 4 | a0001c0001t0001g0037a0001c0001t0001g0099a0001c0001t0001g0287others(1): Show | 4 | HG01074.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-29116_212-2901 others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317606 | |||||
| chr16:24317608
|
A | C | 2 | a0001c0001t0001g0088a0001c0001t0003g0127 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.212-29126A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317608 | ||||||
| chr16:24317610
|
G | GAAAGAAA others(3): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0225 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.212-29116_212-2911 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317610 | |||||
| chr16:24317610
|
GAAAGAAA others(96): Show |
G | 8 | a0001c0001t0001g0044a0001c0001t0001g0129a0001c0001t0001g0162others(5): Show | 8 | HG00323.hp2 HG00738.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-29112_212-2901 others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317610 | |||||
| chr16:24317612
|
A | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0119a0001c0001t0001g0177others(1): Show | 4 | HG01261.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-29122A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317612 | ||||||
| chr16:24317614
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.212-29112_212-2911 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317614 | |||||
| chr16:24317614
|
GAAAGAAA others(92): Show |
G | 16 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0030others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-29108_212-2901 others(103): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317614 | |||||
| chr16:24317616
|
A | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0119others(4): Show | 7 | HG01169.hp1 HG01261.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-29118A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317616 | ||||||
| chr16:24317616
|
AAGAAAGA others(5): Show |
A | 2 | a0001c0001t0001g0204a0001c0001t0001g0284 | 2 | HG00738.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.212-29114_212-2910 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317616 | |||||
| chr16:24317618
|
GAAAGAAA others(88): Show |
G | 20 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0029others(17): Show | 20 | HG00280.hp2 HG00408.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.212-29106_212-2901 others(99): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317618 | |||||
| chr16:24317620
|
A | C | 15 | a0001c0001t0001g0032a0001c0001t0001g0106a0001c0001t0001g0119others(12): Show | 15 | HG00140.hp2 HG01074.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-29114A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317620 | ||||||
| chr16:24317622
|
GAAAGACA others(84): Show |
G | 26 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0085others(23): Show | 26 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.212-29106_212-2901 others(95): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317622 | |||||
| chr16:24317623
|
AAAGACAG others(8): Show |
A | 2 | a0001c0001t0001g0088a0001c0001t0003g0127 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.212-29108_212-2909 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317623 | |||||
| chr16:24317623
|
AAAGACAG others(87): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.212-29108_212-2901 others(98): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317623 | |||||
| chr16:24317624
|
A | AAGAC | 5 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp1 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-29102_212-2909 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317624 | |||||
| chr16:24317624
|
A | C | 17 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0115others(14): Show | 17 | HG00140.hp2 HG01074.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.212-29110A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317624 | ||||||
| chr16:24317626
|
GACAGACA others(80): Show |
G | 30 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0018others(27): Show | 30 | HG00735.hp1 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-29106_212-2902 others(91): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317626 | |||||
| chr16:24317627
|
ACAGACAG others(4): Show |
A | 2 | a0001c0001t0001g0119a0001c0001t0001g0177 | 2 | HG01261.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.212-29106_212-2909 others(15): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317627 | ||||||
| chr16:24317627
|
ACAGACAG others(83): Show |
A | 2 | a0001c0001t0001g0157a0001c0001t0004g0331 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.212-29106_212-2901 others(94): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317627 | ||||||
| chr16:24317628
|
C | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.212-29106C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317628 | ||||||
| chr16:24317630
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.212-29104G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317630 | ||||||
| chr16:24317630
|
GACAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.212-29102_212-2909 others(17): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317630 | |||||
| chr16:24317630
|
GACAGAAA others(76): Show |
G | 19 | a0001c0001t0001g0084a0001c0001t0001g0156a0001c0001t0001g0178others(16): Show | 19 | HG00558.hp2 HG01256.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.212-29102_212-2902 others(87): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317630 | |||||
| chr16:24317631
|
ACAG | A | 5 | a0001c0001t0001g0247a0001c0001t0001g0313a0001c0001t0001g0347others(2): Show | 5 | HG00140.hp2 HG01074.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-29102_212-2910 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317631 | ||||||
| chr16:24317632
|
C | A | 48 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(45): Show | 48 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.212-29102C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317632 | ||||||
| chr16:24317632
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.212-29102C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317632 | ||||||
| chr16:24317632
|
CAGAA | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0131a0001c0001t0001g0149others(2): Show | 5 | HG00558.hp1 HG00673.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-29092_212-2908 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317632 | |||||
| chr16:24317633
|
A | AAG | 3 | a0001c0001t0001g0032a0001c0001t0001g0321a0001c0001t0002g0286 | 3 | HG01433.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.212-29101_212-2910 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317633 | ||||||
| chr16:24317633
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.212-29101A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317633 | ||||||
| chr16:24317634
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0166a0001c0001t0001g0321others(1): Show | 4 | HG01433.hp2 HG03704.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-29100G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317634 | ||||||
| chr16:24317634
|
G | GA | 3 | a0001c0001t0001g0115a0001c0001t0001g0340a0001c0001t0002g0308 | 3 | HG01243.hp2 HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.212-29097dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317634 | |||||
| chr16:24317636
|
A | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0025others(53): Show | 56 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.212-29098A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317636 | ||||||
| chr16:24317638
|
G | GA | 42 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(39): Show | 42 | HG00733.hp2 HG00735.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-29093dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317638 | |||||
| chr16:24317638
|
G | GGA | 7 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0114others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-29096_212-2909 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317638 | ||||||
| chr16:24317638
|
GAAAGAAA others(77): Show |
G | 1 | a0001c0001t0001g0327 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.212-29087_212-2900 others(88): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317638 | |||||
| chr16:24317639
|
AAAGAAAA others(18): Show |
A | 1 | a0001c0001t0001g0140 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-29092_212-2906 others(29): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317639 | |||||
| chr16:24317640
|
A | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0227 | 2 | NA18983.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.212-29094A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317640 | ||||||
| chr16:24317641
|
A | AG | 3 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0001g0355 | 3 | HG00733.hp1 HG01243.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.212-29092dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317641 | |||||
| chr16:24317642
|
G | A | 9 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0247others(6): Show | 9 | HG00140.hp2 HG01074.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-29092G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317642 | ||||||
| chr16:24317642
|
GA | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0227a0001c0001t0001g0307others(1): Show | 4 | HG03654.hp2 HG04228.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-29088delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317642 | |||||
| chr16:24317643
|
A | AAAG | 3 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0172 | 3 | HG01192.hp1 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.212-29089_212-2908 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | AAAGAAAG others(22): Show |
1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.212-29089_212-2908 others(33): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | AAAGAAAG others(14): Show |
1 | a0001c0001t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.212-29089_212-2908 others(25): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | AAAGAAAG others(18): Show |
1 | a0001c0001t0001g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.212-29089_212-2908 others(29): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | AAAGAAAG others(18): Show |
1 | a0001c0001t0001g0077 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.212-29089_212-2908 others(29): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | AAAGAAAG others(14): Show |
1 | a0001c0001t0001g0087 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.212-29089_212-2908 others(25): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317643 | |||||
| chr16:24317643
|
A | G | 13 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0139others(10): Show | 13 | HG00140.hp2 HG00673.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-29091A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317643 | ||||||
| chr16:24317644
|
A | AAG | 9 | a0001c0001t0001g0032a0001c0001t0001g0076a0001c0001t0001g0101others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-29089_212-2908 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317644 | |||||
| chr16:24317644
|
A | AAGAAAGA others(17): Show |
1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.212-29089_212-2908 others(28): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317644 | |||||
| chr16:24317645
|
AAG | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0166a0001c0001t0002g0286others(1): Show | 4 | HG01433.hp2 NA18962.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-29087_212-2908 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317645 | |||||
| chr16:24317646
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0092others(13): Show | 16 | HG00408.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-29088A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317646 | ||||||
| chr16:24317647
|
G | A | 13 | a0001c0001t0001g0032a0001c0001t0001g0076a0001c0001t0001g0101others(10): Show | 13 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-29087G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317647 | ||||||
| chr16:24317647
|
GA | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0088others(24): Show | 27 | HG00140.hp2 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-29083delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317647 | |||||
| chr16:24317648
|
A | AAAAG | 11 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0093others(8): Show | 11 | HG00423.hp2 HG00741.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-29022_212-2901 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAAGAAA others(1): Show |
30 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0033others(27): Show | 30 | HG00544.hp2 HG01069.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.212-29026_212-2901 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAAGAAA others(5): Show |
23 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0091others(20): Show | 23 | HG00408.hp1 HG01106.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.212-29030_212-2901 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAAGAAA others(9): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0200a0001c0001t0001g0273others(1): Show | 4 | HG00544.hp1 HG02027.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-29034_212-2901 others(20): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAAGAAA others(13): Show |
1 | a0001c0001t0001g0218 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.212-29038_212-2901 others(24): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAG | 30 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0028others(27): Show | 30 | HG00733.hp1 HG00735.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.212-29084_212-2908 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAGAAAG | 10 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0098others(7): Show | 10 | HG01243.hp1 HG01928.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-29084_212-2908 others(11): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0309a0001c0001t0002g0154 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.212-29084_212-2908 others(15): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAGAAAG others(8): Show |
1 | a0001c0001t0002g0343 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.212-29084_212-2908 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAGAAAG others(7): Show |
1 | a0001c0001t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.212-29084_212-2908 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAAGGAAA others(5): Show |
1 | a0001c0001t0001g0017 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.212-29084_212-2908 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | AAGAAAGA others(7): Show |
1 | a0001c0001t0001g0014 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.212-29085_212-2908 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
A | G | 17 | a0001c0001t0001g0032a0001c0001t0001g0076a0001c0001t0001g0101others(14): Show | 17 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.212-29086A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317648 | ||||||
| chr16:24317648
|
AAAAG | A | 15 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0118others(12): Show | 15 | HG00140.hp1 HG00558.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-29022_212-2901 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
AAAAGAAA others(1): Show |
A | 8 | a0001c0001t0001g0048a0001c0001t0001g0070a0001c0001t0001g0168others(5): Show | 8 | HG01993.hp2 HG02132.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-29026_212-2901 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317648
|
AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212-29030_212-2901 others(16): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317648 | |||||
| chr16:24317712
|
GA | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0040others(21): Show | 24 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.212-29018delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317712 | |||||
| chr16:24317713
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.212-29019_212-2901 others(15): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24317713 | |||||
| chr16:24317716
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.212-29018A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317716 | ||||||
| chr16:24317717
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.212-29017G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317717 | ||||||
| chr16:24317834
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.212-28900A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317834 | ||||||
| chr16:24317934
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.212-28800T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24317934 | ||||||
| chr16:24318013
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.212-28721T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318013 | ||||||
| chr16:24318014
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.212-28720G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318014 | ||||||
| chr16:24318049
|
T | C | 42 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-28685T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318049 | ||||||
| chr16:24318098
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0003g0224 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.212-28636A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318098 | ||||||
| chr16:24318161
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0290a0001c0001t0001g0299 | 3 | HG02280.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.212-28573G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318161 | ||||||
| chr16:24318183
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.212-28551T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318183 | ||||||
| chr16:24318190
|
T | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.212-28544T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318190 | ||||||
| chr16:24318392
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-28342A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318392 | ||||||
| chr16:24318455
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-28279G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318455 | ||||||
| chr16:24318481
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.212-28253C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318481 | ||||||
| chr16:24318507
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.212-28227G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318507 | ||||||
| chr16:24318610
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.212-28124C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318610 | ||||||
| chr16:24318703
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.212-28031T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318703 | ||||||
| chr16:24318774
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27960T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318774 | ||||||
| chr16:24318919
|
G | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-27815G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318919 | ||||||
| chr16:24318980
|
G | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27754G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24318980 | ||||||
| chr16:24319068
|
T | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27666T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319068 | ||||||
| chr16:24319080
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0234a0001c0001t0001g0287others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-27654G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319080 | ||||||
| chr16:24319256
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0004g0334 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-27478A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319256 | ||||||
| chr16:24319311
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-27423G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319311 | ||||||
| chr16:24319336
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27398T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319336 | ||||||
| chr16:24319358
|
G | C | 2 | a0001c0001t0001g0274a0001c0001t0002g0066 | 2 | NA18942.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.212-27376G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319358 | ||||||
| chr16:24319458
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.212-27276T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319458 | ||||||
| chr16:24319506
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-27228T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319506 | ||||||
| chr16:24319580
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-27154G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319580 | ||||||
| chr16:24319591
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27143C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319591 | ||||||
| chr16:24319608
|
A | ATTT | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.212-27125_212-2712 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24319608 | |||||
| chr16:24319613
|
T | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.212-27121T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319613 | ||||||
| chr16:24319616
|
A | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(231): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.212-27118A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319616 | ||||||
| chr16:24319620
|
T | A | 48 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0052others(45): Show | 48 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.212-27114T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319620 | ||||||
| chr16:24319731
|
G | A | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-27003G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319731 | ||||||
| chr16:24319793
|
G | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.212-26941G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319793 | ||||||
| chr16:24319987
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(208): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.212-26747T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24319987 | ||||||
| chr16:24320113
|
G | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(73): Show | 76 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.212-26621G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320113 | ||||||
| chr16:24320350
|
A | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-26384A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320350 | ||||||
| chr16:24320466
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.212-26268G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320466 | ||||||
| chr16:24320506
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0094a0001c0001t0001g0115others(3): Show | 6 | HG01175.hp1 HG01496.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-26228C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320506 | ||||||
| chr16:24320521
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.212-26213G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320521 | ||||||
| chr16:24320524
|
G | T | 42 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-26210G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320524 | ||||||
| chr16:24320525
|
A | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(65): Show | 68 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.212-26209A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320525 | ||||||
| chr16:24320574
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-26160C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320574 | ||||||
| chr16:24320679
|
G | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(80): Show | 83 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.212-26055G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320679 | ||||||
| chr16:24320748
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(208): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.212-25986G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320748 | ||||||
| chr16:24320782
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0004g0334 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-25952C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320782 | ||||||
| chr16:24320792
|
T | G | 42 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-25942T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320792 | ||||||
| chr16:24320895
|
A | AT | 19 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(16): Show | 19 | HG02135.hp2 HG02165.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.212-25829dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24320895 | |||||
| chr16:24320944
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-25790G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320944 | ||||||
| chr16:24320972
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(262): Show | 265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.212-25762G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24320972 | ||||||
| chr16:24321085
|
GCACCATC others(7): Show |
G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25648_212-2563 others(18): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321085 | ||||||
| chr16:24321109
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25625T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321109 | ||||||
| chr16:24321118
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25616G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321118 | ||||||
| chr16:24321127
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25607A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321127 | ||||||
| chr16:24321140
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25594A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321140 | ||||||
| chr16:24321142
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25592G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321142 | ||||||
| chr16:24321143
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25591C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321143 | ||||||
| chr16:24321144
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25590T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321144 | ||||||
| chr16:24321155
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25579T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321155 | ||||||
| chr16:24321156
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25578A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321156 | ||||||
| chr16:24321157
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25577G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321157 | ||||||
| chr16:24321158
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25576T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321158 | ||||||
| chr16:24321160
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25574A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321160 | ||||||
| chr16:24321161
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25573C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321161 | ||||||
| chr16:24321163
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25571T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321163 | ||||||
| chr16:24321166
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25568C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321166 | ||||||
| chr16:24321168
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25566G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321168 | ||||||
| chr16:24321177
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25557G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321177 | ||||||
| chr16:24321178
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25556T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321178 | ||||||
| chr16:24321192
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25542A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321192 | ||||||
| chr16:24321195
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25539G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321195 | ||||||
| chr16:24321204
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25530G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321204 | ||||||
| chr16:24321218
|
C | T | 43 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0054others(40): Show | 43 | HG00408.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-25516C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321218 | ||||||
| chr16:24321238
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-25496G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321238 | ||||||
| chr16:24321240
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0004g0334 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-25494C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321240 | ||||||
| chr16:24321242
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25492G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321242 | ||||||
| chr16:24321251
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25483C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321251 | ||||||
| chr16:24321253
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25481T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321253 | ||||||
| chr16:24321254
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25480G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321254 | ||||||
| chr16:24321258
|
C | CAGGAGTT others(15): Show |
1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25476_212-2547 others(26): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321258 | ||||||
| chr16:24321262
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25472A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321262 | ||||||
| chr16:24321265
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25469G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321265 | ||||||
| chr16:24321270
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25464A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321270 | ||||||
| chr16:24321276
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.212-25458G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321276 | ||||||
| chr16:24321373
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.212-25361A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321373 | ||||||
| chr16:24321409
|
C | G | 1 | a0001c0001t0002g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.212-25325C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321409 | ||||||
| chr16:24321423
|
G | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(80): Show | 83 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.212-25311G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321423 | ||||||
| chr16:24321437
|
G | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0020others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.212-25297G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321437 | ||||||
| chr16:24321493
|
T | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0211 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.212-25241T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321493 | ||||||
| chr16:24321627
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0232 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.212-25107C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321627 | ||||||
| chr16:24321669
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(206): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-25065A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321669 | ||||||
| chr16:24321854
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(122): Show | 125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.212-24880T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321854 | ||||||
| chr16:24321878
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.212-24856T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321878 | ||||||
| chr16:24321979
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0347 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.212-24755G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24321979 | ||||||
| chr16:24322007
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-24727C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322007 | ||||||
| chr16:24322207
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(256): Show | 259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.212-24527C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322207 | ||||||
| chr16:24322245
|
G | A | 6 | a0001c0001t0001g0095a0001c0001t0001g0123a0001c0001t0001g0158others(3): Show | 6 | HG00733.hp1 HG02258.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-24489G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322245 | ||||||
| chr16:24322393
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.212-24341T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322393 | ||||||
| chr16:24322566
|
T | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-24168T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322566 | ||||||
| chr16:24322668
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0222 | 2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.212-24066C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322668 | ||||||
| chr16:24322733
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-24001G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322733 | ||||||
| chr16:24322763
|
G | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0240a0001c0001t0001g0248others(2): Show | 5 | NA18953.hp2 NA19056.hp2 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-23971G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24322763 | ||||||
| chr16:24323219
|
C | CA | 14 | a0001c0001t0001g0063a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | HG00544.hp1 HG00544.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-23494dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323219 | |||||
| chr16:24323219
|
C | CAA | 39 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(36): Show | 39 | HG00558.hp2 HG00738.hp1 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.212-23495_212-2349 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323219 | |||||
| chr16:24323219
|
C | CAAA | 89 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.212-23496_212-2349 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323219 | |||||
| chr16:24323219
|
C | CAAAA | 8 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0172others(5): Show | 8 | HG01361.hp1 HG01884.hp1 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-23497_212-2349 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323219 | |||||
| chr16:24323237
|
A | AG | 3 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0283 | 3 | HG01175.hp1 HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.212-23497_212-2349 others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323237 | ||||||
| chr16:24323237
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.212-23497A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323237 | ||||||
| chr16:24323239
|
A | AAG | 6 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0196others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-23483_212-2348 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323239 | |||||
| chr16:24323239
|
A | G | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-23495A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323239 | ||||||
| chr16:24323239
|
AAG | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(106): Show | 109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.212-23483_212-2348 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24323239 | |||||
| chr16:24323240
|
AG | A | 10 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-23493delG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323240 | ||||||
| chr16:24323240
|
AGAG | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0292a0001c0001t0001g0309others(1): Show | 4 | HG01515.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-23493_212-2349 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323240 | ||||||
| chr16:24323243
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(116): Show | 119 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.212-23491G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323243 | ||||||
| chr16:24323777
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-22957T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323777 | ||||||
| chr16:24323828
|
A | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-22906A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323828 | ||||||
| chr16:24323858
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0198others(2): Show | 5 | HG01175.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-22876C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323858 | ||||||
| chr16:24323905
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.212-22829T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323905 | ||||||
| chr16:24323914
|
C | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0110 | 2 | NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.212-22820C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323914 | ||||||
| chr16:24323982
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.212-22752G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24323982 | ||||||
| chr16:24324008
|
T | C | 1 | a0001c0001t0002g0343 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.212-22726T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324008 | ||||||
| chr16:24324131
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.212-22603G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324131 | ||||||
| chr16:24324351
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.212-22383T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324351 | ||||||
| chr16:24324363
|
C | T | 99 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.212-22371C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324363 | ||||||
| chr16:24324511
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.212-22223G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324511 | ||||||
| chr16:24324603
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.212-22131T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324603 | ||||||
| chr16:24324649
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.212-22085C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324649 | ||||||
| chr16:24324778
|
G | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0297a0001c0002t0001g0361 | 3 | HG02280.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.212-21956G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324778 | ||||||
| chr16:24324792
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.212-21942C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324792 | ||||||
| chr16:24324887
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.212-21847G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24324887 | ||||||
| chr16:24325448
|
C | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0163others(2): Show | 5 | HG01070.hp2 HG01943.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-21286C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325448 | ||||||
| chr16:24325825
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.212-20909G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325825 | ||||||
| chr16:24325834
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-20900A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325834 | ||||||
| chr16:24325900
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.212-20834G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325900 | ||||||
| chr16:24325905
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-20829A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325905 | ||||||
| chr16:24325960
|
T | TCAAGCAT others(23): Show |
1 | a0001c0001t0002g0286 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.212-20773_212-2074 others(34): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24325960 | |||||
| chr16:24325967
|
T | C | 1 | a0001c0001t0004g0334 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.212-20767T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24325967 | ||||||
| chr16:24326167
|
C | G | 1 | a0001c0001t0001g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.212-20567C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326167 | ||||||
| chr16:24326174
|
CTT | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(240): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.212-20547_212-2054 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24326174 | |||||
| chr16:24326196
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0207a0001c0001t0001g0218 | 3 | NA18974.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.212-20538A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326196 | ||||||
| chr16:24326202
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0004g0331 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.212-20532G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326202 | ||||||
| chr16:24326361
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(73): Show | 76 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.212-20373G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326361 | ||||||
| chr16:24326390
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-20344C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326390 | ||||||
| chr16:24326402
|
C | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(226): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.212-20332C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326402 | ||||||
| chr16:24326700
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-20034A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326700 | ||||||
| chr16:24326727
|
C | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-20007C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326727 | ||||||
| chr16:24326788
|
C | T | 27 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-19946C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326788 | ||||||
| chr16:24326903
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.212-19831T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24326903 | ||||||
| chr16:24327036
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-19698C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327036 | ||||||
| chr16:24327082
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.212-19652G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327082 | ||||||
| chr16:24327099
|
G | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-19635G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327099 | ||||||
| chr16:24327100
|
G | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0078others(5): Show | 8 | NA18953.hp1 NA18955.hp2 NA19012.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-19634G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327100 | ||||||
| chr16:24327126
|
C | CA | 54 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0048others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.212-19581dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
C | CAA | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.212-19582_212-1958 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
C | CAAA | 33 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(30): Show | 33 | HG00673.hp2 HG00735.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.212-19583_212-1958 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
C | CAAAA | 8 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0075others(5): Show | 8 | HG01069.hp2 HG01192.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-19584_212-1958 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
C | CAAAAA | 9 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0137others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-19585_212-1958 others(9): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
CA | C | 7 | a0001c0001t0001g0156a0001c0001t0001g0182a0001c0001t0001g0194others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-19581delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
CAAA | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(14): Show | 17 | HG00735.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.212-19583_212-1958 others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
CAAAA | C | 93 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0032others(90): Show | 93 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.212-19584_212-1958 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327126
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.212-19595_212-1958 others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327126 | |||||
| chr16:24327165
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-19569G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327165 | ||||||
| chr16:24327193
|
G | GGC | 27 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-19540_212-1953 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327193 | |||||
| chr16:24327422
|
A | ATATG | 3 | a0001c0001t0001g0021a0001c0001t0001g0247a0001c0001t0001g0279 | 3 | NA18951.hp1 NA18959.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.212-19311_212-1931 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327422
|
A | ATG | 75 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(72): Show | 75 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.212-19296_212-1929 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327422
|
A | ATGTG | 26 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0073others(23): Show | 26 | HG00733.hp2 HG00738.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.212-19298_212-1929 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327422
|
A | ATGTGTG | 8 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG02155.hp1 HG02738.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-19300_212-1929 others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327422
|
A | ATGTGTGT others(1): Show |
23 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(20): Show | 23 | HG00558.hp2 HG02027.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-19302_212-1929 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327422
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0349 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.212-19304_212-1929 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327422 | |||||
| chr16:24327438
|
G | A | 7 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0001t0001g0168others(4): Show | 7 | HG00741.hp1 HG01109.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-19296G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327438 | ||||||
| chr16:24327438
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0002g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.212-19295_212-1929 others(26): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327438 | |||||
| chr16:24327440
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.212-19294A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327440 | ||||||
| chr16:24327441
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-19291_212-1927 others(22): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327441 | |||||
| chr16:24327442
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(253): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.212-19292A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327442 | ||||||
| chr16:24327444
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(251): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.212-19290A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327444 | ||||||
| chr16:24327446
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.212-19288A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327446 | ||||||
| chr16:24327448
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.212-19286A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327448 | ||||||
| chr16:24327450
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(197): Show | 200 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.212-19284A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327450 | ||||||
| chr16:24327452
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(121): Show | 124 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.212-19282A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327452 | ||||||
| chr16:24327453
|
TATACACA others(1): Show |
T | 14 | a0001c0001t0001g0010a0001c0001t0001g0059a0001c0001t0001g0099others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-19279_212-1927 others(12): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327453 | |||||
| chr16:24327454
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0125others(13): Show | 16 | HG00673.hp1 HG01175.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-19280A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327454 | ||||||
| chr16:24327455
|
T | C | 5 | a0001c0001t0001g0168a0001c0001t0001g0199a0001c0001t0001g0212others(2): Show | 5 | HG02976.hp1 HG03195.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-19279T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327455 | ||||||
| chr16:24327455
|
T | TAC | 4 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0093others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-19257_212-1925 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327455 | |||||
| chr16:24327455
|
TAC | T | 12 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG00408.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-19257_212-1925 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327455 | |||||
| chr16:24327455
|
TACAC | T | 29 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-19259_212-1925 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327455 | |||||
| chr16:24327456
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-19278A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327456 | ||||||
| chr16:24327457
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.212-19277C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327457 | ||||||
| chr16:24327459
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.212-19275C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327459 | ||||||
| chr16:24327461
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(226): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.212-19273C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327461 | ||||||
| chr16:24327463
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0126others(4): Show | 7 | HG02486.hp1 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-19271C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327463 | ||||||
| chr16:24327543
|
T | A | 1 | a0001c0001t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.212-19191T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327543 | ||||||
| chr16:24327619
|
C | CA | 11 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0099others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-19107dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327619 | |||||
| chr16:24327629
|
AAAAACAA others(3): Show |
A | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-19090_212-1908 others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24327629 | |||||
| chr16:24327688
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.212-19046T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327688 | ||||||
| chr16:24327722
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(19): Show | 22 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.212-19012G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327722 | ||||||
| chr16:24327942
|
A | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.212-18792A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24327942 | ||||||
| chr16:24328385
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(109): Show | 112 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.212-18349G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328385 | ||||||
| chr16:24328454
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-18280G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328454 | ||||||
| chr16:24328466
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.212-18268C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328466 | ||||||
| chr16:24328471
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.212-18263A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328471 | ||||||
| chr16:24328512
|
C | A | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.212-18222C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328512 | ||||||
| chr16:24328607
|
TA | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0059others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-18124delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24328607 | |||||
| chr16:24328612
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(206): Show | 209 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.212-18122A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328612 | ||||||
| chr16:24328771
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212-17963G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328771 | ||||||
| chr16:24328817
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.212-17917C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328817 | ||||||
| chr16:24328822
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.212-17912G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328822 | ||||||
| chr16:24328860
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.212-17874G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328860 | ||||||
| chr16:24328944
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.212-17790C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328944 | ||||||
| chr16:24328968
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.212-17766C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24328968 | ||||||
| chr16:24329239
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0059others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-17495G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329239 | ||||||
| chr16:24329281
|
T | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(19): Show | 22 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.212-17453T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329281 | ||||||
| chr16:24329344
|
C | G | 1 | a0001c0002t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.212-17390C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329344 | ||||||
| chr16:24329370
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(272): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.212-17364A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329370 | ||||||
| chr16:24329447
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0003g0202 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.212-17287G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329447 | ||||||
| chr16:24329641
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0290a0001c0001t0001g0299 | 3 | HG02280.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.212-17093A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329641 | ||||||
| chr16:24329659
|
C | T | 1 | a0001c0001t0004g0334 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.212-17075C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329659 | ||||||
| chr16:24329766
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-16968G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329766 | ||||||
| chr16:24329867
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-16867C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329867 | ||||||
| chr16:24329943
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0348 | 2 | NA18953.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.212-16791C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24329943 | ||||||
| chr16:24330091
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.212-16643A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330091 | ||||||
| chr16:24330121
|
C | G | 7 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0151others(4): Show | 7 | HG00408.hp1 HG00673.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-16613C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330121 | ||||||
| chr16:24330156
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0002g0045 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-16578C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330156 | ||||||
| chr16:24330157
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0336 | 2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.212-16577G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330157 | ||||||
| chr16:24330241
|
G | A | 55 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.212-16493G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330241 | ||||||
| chr16:24330430
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0059others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-16304A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330430 | ||||||
| chr16:24330470
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0002g0310others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-16264A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330470 | ||||||
| chr16:24330488
|
C | T | 29 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-16246C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330488 | ||||||
| chr16:24330508
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0144a0001c0001t0001g0157others(1): Show | 4 | HG01361.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-16226G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330508 | ||||||
| chr16:24330858
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-15876A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330858 | ||||||
| chr16:24330871
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0004g0332 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-15863G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24330871 | ||||||
| chr16:24331141
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-15593G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331141 | ||||||
| chr16:24331142
|
C | A | 1 | a0001c0001t0001g0341 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.212-15592C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331142 | ||||||
| chr16:24331185
|
G | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(20): Show | 23 | HG00558.hp2 HG01358.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-15549G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331185 | ||||||
| chr16:24331210
|
C | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.212-15524C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331210 | ||||||
| chr16:24331231
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0045 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-15503G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331231 | ||||||
| chr16:24331282
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.212-15452G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331282 | ||||||
| chr16:24331367
|
T | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(272): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.212-15367T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331367 | ||||||
| chr16:24331526
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.212-15208A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331526 | ||||||
| chr16:24331603
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.212-15131T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331603 | ||||||
| chr16:24331617
|
T | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(20): Show | 23 | HG00558.hp2 HG01358.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-15117T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331617 | ||||||
| chr16:24331843
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.212-14891C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331843 | ||||||
| chr16:24331849
|
T | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(82): Show | 85 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.212-14885T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331849 | ||||||
| chr16:24331917
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0137others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-14817A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24331917 | ||||||
| chr16:24332015
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.212-14719G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332015 | ||||||
| chr16:24332067
|
A | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0199a0001c0001t0001g0212others(1): Show | 4 | HG03195.hp2 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-14667A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332067 | ||||||
| chr16:24332078
|
G | A | 29 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-14656G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332078 | ||||||
| chr16:24332150
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0296 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.212-14584A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332150 | ||||||
| chr16:24332442
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.212-14292G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332442 | ||||||
| chr16:24332464
|
C | CA | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(250): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.212-14255dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24332464 | |||||
| chr16:24332464
|
C | CAA | 24 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(21): Show | 24 | HG00558.hp2 HG01261.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.212-14256_212-1425 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24332464 | |||||
| chr16:24332583
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.212-14151C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332583 | ||||||
| chr16:24332668
|
T | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0128others(2): Show | 5 | HG00642.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-14066T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24332668 | ||||||
| chr16:24333385
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0003g0127 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.212-13349T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24333385 | ||||||
| chr16:24333556
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0002g0310others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-13178T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24333556 | ||||||
| chr16:24333672
|
C | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0287others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-13062C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24333672 | ||||||
| chr16:24334011
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.212-12723T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334011 | ||||||
| chr16:24334167
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG00673.hp2 NA19012.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-12567A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334167 | ||||||
| chr16:24334180
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0363 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-12554C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334180 | ||||||
| chr16:24334200
|
T | A | 1 | a0001c0001t0001g0284 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.212-12534T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334200 | ||||||
| chr16:24334391
|
A | G | 18 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0129others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-12343A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334391 | ||||||
| chr16:24334440
|
C | T | 77 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 77 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.212-12294C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334440 | ||||||
| chr16:24334505
|
T | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0074a0001c0001t0001g0075others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-12229T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334505 | ||||||
| chr16:24334526
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.212-12208C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334526 | ||||||
| chr16:24334558
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.212-12176G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334558 | ||||||
| chr16:24334700
|
C | T | 1 | a0001c0001t0001g0353 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.212-12034C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334700 | ||||||
| chr16:24334798
|
T | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 77 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.212-11936T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334798 | ||||||
| chr16:24334879
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0002g0310others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-11855A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24334879 | ||||||
| chr16:24335096
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.212-11638G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335096 | ||||||
| chr16:24335173
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.212-11561G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335173 | ||||||
| chr16:24335190
|
C | G | 1 | a0001c0001t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.212-11544C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335190 | ||||||
| chr16:24335249
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.212-11485G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335249 | ||||||
| chr16:24335312
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-11422C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335312 | ||||||
| chr16:24335386
|
C | G | 1 | a0001c0001t0001g0021 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.212-11348C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335386 | ||||||
| chr16:24335558
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.212-11176T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335558 | ||||||
| chr16:24335637
|
T | G | 30 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0090others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-11097T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335637 | ||||||
| chr16:24335867
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212-10867G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335867 | ||||||
| chr16:24335935
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.212-10799C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24335935 | ||||||
| chr16:24335935
|
CA | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.212-10789delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24335935 | |||||
| chr16:24336140
|
G | A | 77 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 77 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.212-10594G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336140 | ||||||
| chr16:24336212
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.212-10522A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336212 | ||||||
| chr16:24336251
|
C | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-10483C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336251 | ||||||
| chr16:24336275
|
A | AT | 27 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(24): Show | 27 | HG00099.hp2 HG00423.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-10445dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24336275 | |||||
| chr16:24336275
|
AT | A | 39 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.212-10445delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24336275 | |||||
| chr16:24336323
|
C | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.212-10411C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336323 | ||||||
| chr16:24336332
|
C | T | 1 | a0001c0001t0001g0359 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.212-10402C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336332 | ||||||
| chr16:24336421
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-10313G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336421 | ||||||
| chr16:24336563
|
CT | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(249): Show | 252 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.212-10170delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336563 | ||||||
| chr16:24336565
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212-10169G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336565 | ||||||
| chr16:24336642
|
A | ACT | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10092_212-1009 others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336642 | ||||||
| chr16:24336644
|
A | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10090A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336644 | ||||||
| chr16:24336647
|
T | G | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10087T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336647 | ||||||
| chr16:24336650
|
G | GCCAAGGT others(342): Show |
1 | a0001c0001t0001g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.212-10084_212-1008 others(353): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336650 | ||||||
| chr16:24336650
|
G | GCCAAGGT others(342): Show |
30 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-10084_212-1008 others(353): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336650 | ||||||
| chr16:24336650
|
G | GCCAAGGT others(340): Show |
1 | a0001c0001t0002g0022 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.212-10084_212-1008 others(351): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336650 | ||||||
| chr16:24336653
|
C | CGCCA | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10081_212-1008 others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336653 | ||||||
| chr16:24336655
|
T | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10079T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336655 | ||||||
| chr16:24336656
|
G | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10078G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336656 | ||||||
| chr16:24336659
|
A | C | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-10075A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336659 | ||||||
| chr16:24336895
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.212-9839G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336895 | ||||||
| chr16:24336911
|
C | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-9823C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336911 | ||||||
| chr16:24336951
|
A | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0137others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-9783A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24336951 | ||||||
| chr16:24337071
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.212-9663C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337071 | ||||||
| chr16:24337074
|
A | T | 88 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0017others(85): Show | 88 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.212-9660A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337074 | ||||||
| chr16:24337237
|
A | G | 2 | a0001c0001t0001g0063a0001c0002t0001g0009 | 2 | HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.212-9497A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337237 | ||||||
| chr16:24337270
|
G | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.212-9464G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337270 | ||||||
| chr16:24337466
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-9268T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337466 | ||||||
| chr16:24337534
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0045 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-9200G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337534 | ||||||
| chr16:24337650
|
T | TTAA | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-9061_212-9059d others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24337650 | |||||
| chr16:24337741
|
T | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0249a0001c0001t0001g0337 | 3 | NA18941.hp2 NA18960.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.212-8993T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337741 | ||||||
| chr16:24337789
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-8945T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337789 | ||||||
| chr16:24337819
|
A | T | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-8915A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337819 | ||||||
| chr16:24337998
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0222 | 2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.212-8736C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24337998 | ||||||
| chr16:24338071
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212-8663C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338071 | ||||||
| chr16:24338092
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.212-8642C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338092 | ||||||
| chr16:24338104
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.212-8630C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338104 | ||||||
| chr16:24338120
|
T | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0309 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.212-8614T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338120 | ||||||
| chr16:24338199
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0002g0045 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-8535A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338199 | ||||||
| chr16:24338446
|
T | A | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-8288T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338446 | ||||||
| chr16:24338709
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0004g0331 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.212-8025C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338709 | ||||||
| chr16:24338730
|
G | A | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-8004G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24338730 | ||||||
| chr16:24339111
|
C | CT | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-7622dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24339111 | |||||
| chr16:24339119
|
T | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0241a0001c0001t0001g0289 | 3 | NA18946.hp1 NA18997.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.212-7615T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339119 | ||||||
| chr16:24339218
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-7516T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339218 | ||||||
| chr16:24339282
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.212-7452T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339282 | ||||||
| chr16:24339298
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-7436G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339298 | ||||||
| chr16:24339357
|
TC | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-7376delC | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339357 | ||||||
| chr16:24339358
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(248): Show | 251 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.212-7376C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339358 | ||||||
| chr16:24339553
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.212-7181T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339553 | ||||||
| chr16:24339589
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0222 | 2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.212-7145C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339589 | ||||||
| chr16:24339666
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0304a0001c0001t0001g0317others(2): Show | 5 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-7068G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339666 | ||||||
| chr16:24339799
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0269others(3): Show | 6 | HG02486.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-6935G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339799 | ||||||
| chr16:24339899
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212-6835A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24339899 | ||||||
| chr16:24340007
|
C | A | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-6727C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340007 | ||||||
| chr16:24340095
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.212-6639C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340095 | ||||||
| chr16:24340130
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.212-6604T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340130 | ||||||
| chr16:24340162
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(281): Show | 284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.212-6572A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340162 | ||||||
| chr16:24340330
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.212-6404C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340330 | ||||||
| chr16:24340331
|
G | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0017others(78): Show | 81 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.212-6403G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340331 | ||||||
| chr16:24340379
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.212-6355C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340379 | ||||||
| chr16:24340385
|
G | A | 35 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(32): Show | 35 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.212-6349G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340385 | ||||||
| chr16:24340389
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0003g0202 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.212-6345C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340389 | ||||||
| chr16:24340392
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.212-6342C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340392 | ||||||
| chr16:24340393
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0336 | 2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.212-6341G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340393 | ||||||
| chr16:24340523
|
A | T | 99 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(96): Show | 99 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.212-6211A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340523 | ||||||
| chr16:24340648
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212-6086A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340648 | ||||||
| chr16:24340654
|
A | G | 34 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-6080A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340654 | ||||||
| chr16:24340715
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.212-6019C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340715 | ||||||
| chr16:24340719
|
T | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.212-6015T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340719 | ||||||
| chr16:24340721
|
A | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0119a0001c0001t0001g0330 | 3 | HG01261.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.212-6013A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340721 | ||||||
| chr16:24340828
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.212-5906G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340828 | ||||||
| chr16:24340887
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.212-5847G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340887 | ||||||
| chr16:24340934
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0285a0001c0001t0001g0340 | 3 | HG01243.hp2 HG01346.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.212-5800C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24340934 | ||||||
| chr16:24341047
|
G | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0185 | 2 | HG00099.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.212-5687G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341047 | ||||||
| chr16:24341074
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-5660T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341074 | ||||||
| chr16:24341348
|
T | G | 1 | a0001c0001t0001g0358 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.212-5386T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341348 | ||||||
| chr16:24341372
|
T | TA | 3 | a0001c0001t0001g0058a0001c0001t0001g0185a0001c0001t0002g0045 | 3 | HG00099.hp2 HG01069.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.212-5358dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24341372 | |||||
| chr16:24341433
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-5301G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341433 | ||||||
| chr16:24341607
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.212-5127T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341607 | ||||||
| chr16:24341641
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0078a0001c0001t0001g0111 | 3 | NA18955.hp2 NA19012.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.212-5093G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341641 | ||||||
| chr16:24341750
|
C | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.212-4984C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341750 | ||||||
| chr16:24341751
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0005g0008 | 2 | NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.212-4983G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341751 | ||||||
| chr16:24341753
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.212-4981G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341753 | ||||||
| chr16:24341758
|
G | C | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-4976G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341758 | ||||||
| chr16:24341890
|
G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0163a0001c0001t0001g0186others(1): Show | 4 | HG01070.hp2 HG01943.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-4844G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341890 | ||||||
| chr16:24341936
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.212-4798G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24341936 | ||||||
| chr16:24342036
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 155 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.212-4698A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342036 | ||||||
| chr16:24342041
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0293a0001c0001t0004g0332 | 3 | HG01934.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.212-4693G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342041 | ||||||
| chr16:24342051
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.212-4683T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342051 | ||||||
| chr16:24342084
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-4650A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342084 | ||||||
| chr16:24342125
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0123a0001c0001t0001g0158others(2): Show | 5 | HG00733.hp1 HG02738.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-4609G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342125 | ||||||
| chr16:24342471
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.212-4263A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342471 | ||||||
| chr16:24342681
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.212-4053A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342681 | ||||||
| chr16:24342810
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.212-3924T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342810 | ||||||
| chr16:24342886
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.212-3848C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342886 | ||||||
| chr16:24342916
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-3818G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342916 | ||||||
| chr16:24342953
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0137others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-3781G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342953 | ||||||
| chr16:24342979
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0185others(5): Show | 8 | HG00099.hp2 HG01069.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-3755C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24342979 | ||||||
| chr16:24343120
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0328 | 2 | HG02165.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.212-3614C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343120 | ||||||
| chr16:24343276
|
C | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(147): Show | 150 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.212-3458C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343276 | ||||||
| chr16:24343508
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 154 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.212-3226T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343508 | ||||||
| chr16:24343509
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0296 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.212-3225G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343509 | ||||||
| chr16:24343586
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.212-3148G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343586 | ||||||
| chr16:24343800
|
G | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.212-2934G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343800 | ||||||
| chr16:24343834
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0157 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212-2900A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343834 | ||||||
| chr16:24343895
|
C | A | 127 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.212-2839C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24343895 | ||||||
| chr16:24344157
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.212-2577C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344157 | ||||||
| chr16:24344311
|
T | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.212-2423T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344311 | ||||||
| chr16:24344362
|
T | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0222 | 2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.212-2372T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344362 | ||||||
| chr16:24344410
|
G | GA | 77 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0021others(74): Show | 77 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.212-2310dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24344410 | |||||
| chr16:24344410
|
GA | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.212-2310delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24344410 | |||||
| chr16:24344410
|
GAA | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0102a0001c0001t0001g0169others(8): Show | 11 | HG02015.hp2 HG02155.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-2311_212-2310d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24344410 | |||||
| chr16:24344447
|
C | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0088a0001c0001t0001g0177others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-2287C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344447 | ||||||
| chr16:24344469
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.212-2265C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344469 | ||||||
| chr16:24344483
|
T | C | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-2251T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344483 | ||||||
| chr16:24344496
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.212-2238C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344496 | ||||||
| chr16:24344513
|
G | C | 1 | a0001c0001t0001g0355 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.212-2221G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344513 | ||||||
| chr16:24344635
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.212-2099T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344635 | ||||||
| chr16:24344849
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0002g0251 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.212-1885C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344849 | ||||||
| chr16:24344861
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.212-1873C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344861 | ||||||
| chr16:24344929
|
G | A | 105 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.212-1805G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344929 | ||||||
| chr16:24344970
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-1764A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24344970 | ||||||
| chr16:24345195
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.212-1539G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345195 | ||||||
| chr16:24345212
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.212-1522C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345212 | ||||||
| chr16:24345243
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-1491T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345243 | ||||||
| chr16:24345254
|
C | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0084a0001c0001t0001g0099others(11): Show | 14 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.212-1480C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345254 | ||||||
| chr16:24345303
|
T | A | 3 | a0001c0001t0002g0310a0001c0001t0002g0312a0001c0001t0002g0316 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-1431T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345303 | ||||||
| chr16:24345517
|
A | C | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-1217A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345517 | ||||||
| chr16:24345556
|
C | T | 6 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-1178C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345556 | ||||||
| chr16:24345649
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-1085G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345649 | ||||||
| chr16:24345679
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0033others(48): Show | 51 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.212-1055G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345679 | ||||||
| chr16:24345681
|
C | G | 2 | a0001c0001t0004g0331a0001c0003t0001g0237 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.212-1053C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345681 | ||||||
| chr16:24345776
|
G | A | 2 | a0001c0001t0004g0331a0001c0003t0001g0237 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.212-958G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345776 | ||||||
| chr16:24345790
|
C | T | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-944C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345790 | ||||||
| chr16:24345859
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0333 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.212-875A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345859 | ||||||
| chr16:24345874
|
G | T | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-860G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345874 | ||||||
| chr16:24345962
|
A | C | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.212-772A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24345962 | ||||||
| chr16:24346161
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.212-573C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346161 | ||||||
| chr16:24346511
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212-223A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346511 | ||||||
| chr16:24346615
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-119A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346615 | ||||||
| chr16:24346631
|
C | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-103C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346631 | ||||||
| chr16:24346635
|
C | T | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.212-99C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346635 | ||||||
| chr16:24346662
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.212-72G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346662 | ||||||
| chr16:24346677
|
T | TG | 346 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(343): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.212-55dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 24346677 | |||||
| chr16:24346685
|
A | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.212-49A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 1/3 | chr16 | 24346685 | ||||||
| chr16:24346865
|
T | C | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.295+48T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24346865 | ||||||
| chr16:24346897
|
C | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.295+80C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24346897 | ||||||
| chr16:24346923
|
A | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.295+106A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24346923 | ||||||
| chr16:24346998
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.295+181T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24346998 | ||||||
| chr16:24347004
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.295+187G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347004 | ||||||
| chr16:24347348
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0223 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295+531G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347348 | ||||||
| chr16:24347413
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.295+596G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347413 | ||||||
| chr16:24347475
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295+658A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347475 | ||||||
| chr16:24347541
|
G | C | 1 | a0001c0001t0001g0321 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.295+724G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347541 | ||||||
| chr16:24347553
|
G | A | 2 | a0001c0001t0001g0358a0001c0001t0002g0022 | 2 | NA18974.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.295+736G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347553 | ||||||
| chr16:24347593
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+776A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347593 | ||||||
| chr16:24347598
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.295+781G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347598 | ||||||
| chr16:24347636
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.295+819C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347636 | ||||||
| chr16:24347639
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.295+822C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347639 | ||||||
| chr16:24347693
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+876A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347693 | ||||||
| chr16:24347722
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.295+905C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347722 | ||||||
| chr16:24347730
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295+913C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347730 | ||||||
| chr16:24347777
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0002g0310others(2): Show | 5 | HG02622.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+960C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347777 | ||||||
| chr16:24347821
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0223 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295+1004G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347821 | ||||||
| chr16:24347866
|
C | A | 1 | a0001c0001t0004g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295+1049C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347866 | ||||||
| chr16:24347922
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0333 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.295+1105C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24347922 | ||||||
| chr16:24348112
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.295+1295G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348112 | ||||||
| chr16:24348238
|
A | AT | 69 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0023others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.295+1434dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24348238 | |||||
| chr16:24348238
|
AT | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+1434delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24348238 | |||||
| chr16:24348283
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+1466G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348283 | ||||||
| chr16:24348354
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.295+1537C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348354 | ||||||
| chr16:24348356
|
G | GTGATCGT others(10): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0211 | 3 | HG02630.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.295+1544_295+1560d others(19): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24348356 | |||||
| chr16:24348362
|
G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(12): Show | 15 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.295+1545G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348362 | ||||||
| chr16:24348389
|
G | A | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+1572G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348389 | ||||||
| chr16:24348424
|
G | A | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+1607G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348424 | ||||||
| chr16:24348607
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.295+1790G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348607 | ||||||
| chr16:24348625
|
T | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0245 | 2 | NA18948.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.295+1808T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348625 | ||||||
| chr16:24348753
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.295+1936A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348753 | ||||||
| chr16:24348889
|
T | G | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2072T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24348889 | ||||||
| chr16:24349024
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(12): Show | 15 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.295+2207A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349024 | ||||||
| chr16:24349052
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295+2235C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349052 | ||||||
| chr16:24349116
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.295+2299G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349116 | ||||||
| chr16:24349152
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.295+2335C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349152 | ||||||
| chr16:24349198
|
T | C | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2381T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349198 | ||||||
| chr16:24349222
|
C | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(12): Show | 15 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.295+2405C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349222 | ||||||
| chr16:24349225
|
CT | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+2412delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24349225 | |||||
| chr16:24349306
|
A | G | 2 | a0001c0001t0004g0331a0001c0003t0001g0237 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.295+2489A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349306 | ||||||
| chr16:24349453
|
A | G | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2636A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349453 | ||||||
| chr16:24349611
|
C | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+2794C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349611 | ||||||
| chr16:24349706
|
C | T | 1 | a0001c0001t0001g0359 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.295+2889C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349706 | ||||||
| chr16:24349929
|
G | A | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+3112G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24349929 | ||||||
| chr16:24350014
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.295+3197C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350014 | ||||||
| chr16:24350029
|
T | C | 1 | a0001c0002t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295+3212T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350029 | ||||||
| chr16:24350040
|
G | GA | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+3223_295+3224i others(3): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350040 | ||||||
| chr16:24350274
|
G | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0194others(4): Show | 7 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+3457G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350274 | ||||||
| chr16:24350316
|
C | CT | 27 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(24): Show | 27 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.295+3515dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24350316 | |||||
| chr16:24350316
|
CT | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0123others(8): Show | 11 | HG00733.hp1 HG02735.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+3515delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24350316 | |||||
| chr16:24350384
|
A | C | 8 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0117others(5): Show | 8 | HG02071.hp1 HG03017.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+3567A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350384 | ||||||
| chr16:24350550
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.295+3733C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350550 | ||||||
| chr16:24350582
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0085others(26): Show | 29 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.295+3765G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350582 | ||||||
| chr16:24350630
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0161a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+3813A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350630 | ||||||
| chr16:24350722
|
T | G | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+3905T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24350722 | ||||||
| chr16:24351014
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(14): Show | 17 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-3819T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351014 | ||||||
| chr16:24351216
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.296-3617G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351216 | ||||||
| chr16:24351252
|
A | T | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.296-3581A>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351252 | ||||||
| chr16:24351292
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0002g0251 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.296-3541C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351292 | ||||||
| chr16:24351310
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.296-3523C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351310 | ||||||
| chr16:24351507
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.296-3326G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351507 | ||||||
| chr16:24351526
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.296-3307G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351526 | ||||||
| chr16:24351557
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3276C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351557 | ||||||
| chr16:24351586
|
A | AGGAAGG | 14 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0037others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-3216_296-3211d others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351586 | |||||
| chr16:24351586
|
AGGAAGG | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0028others(41): Show | 44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-3216_296-3211d others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351586 | |||||
| chr16:24351586
|
AGGAAGGG others(5): Show |
A | 2 | a0001c0001t0001g0143a0001c0001t0001g0333 | 2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.296-3222_296-3211d others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351586 | |||||
| chr16:24351620
|
A | AGGGGAG | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3211_296-3210i others(8): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351620 | |||||
| chr16:24351648
|
G | GGAA | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3184_296-3183i others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351648 | |||||
| chr16:24351654
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3179A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351654 | ||||||
| chr16:24351656
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3177A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351656 | ||||||
| chr16:24351657
|
C | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3176C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351657 | ||||||
| chr16:24351658
|
A | AG | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3174dupG | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351658 | |||||
| chr16:24351660
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3173A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351660 | ||||||
| chr16:24351661
|
C | A | 2 | a0001c0001t0004g0331a0001c0003t0001g0237 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.296-3172C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351661 | ||||||
| chr16:24351661
|
C | CGAAA | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.296-3152_296-3149d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351661 | |||||
| chr16:24351661
|
C | CGAAAGAA others(1): Show |
54 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.296-3156_296-3149d others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351661 | |||||
| chr16:24351661
|
C | CGAAAGAA others(5): Show |
2 | a0001c0001t0001g0101a0001c0001t0002g0110 | 2 | NA18956.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.296-3160_296-3149d others(14): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351661 | |||||
| chr16:24351661
|
C | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-3172C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351661 | ||||||
| chr16:24351661
|
CGAAA | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0168a0001c0001t0001g0180others(6): Show | 9 | HG01109.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-3152_296-3149d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351661 | |||||
| chr16:24351665
|
A | AGAAAGAA others(17): Show |
1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.296-3149_296-3148i others(26): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351665 | |||||
| chr16:24351667
|
A | ACAG | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(14): Show | 17 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-3166_296-3165i others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351667 | ||||||
| chr16:24351668
|
A | C | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.296-3165A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351668 | ||||||
| chr16:24351669
|
A | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(14): Show | 17 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-3164A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351669 | ||||||
| chr16:24351673
|
A | C | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.296-3160A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351673 | ||||||
| chr16:24351685
|
G | A | 93 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.296-3148G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351685 | ||||||
| chr16:24351689
|
A | AGAAG | 4 | a0001c0001t0001g0321a0001c0001t0002g0068a0001c0001t0002g0171others(1): Show | 4 | HG02735.hp2 HG03704.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3141_296-3140i others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351689 | |||||
| chr16:24351689
|
A | G | 89 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.296-3144A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351689 | ||||||
| chr16:24351700
|
G | A | 93 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.296-3133G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351700 | ||||||
| chr16:24351702
|
A | G | 93 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.296-3131A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351702 | ||||||
| chr16:24351713
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.296-3120A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351713 | ||||||
| chr16:24351724
|
G | GGA | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0168others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.296-3098_296-3097d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351724 | |||||
| chr16:24351757
|
A | AAGAG | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.296-3066_296-3063d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351757 | |||||
| chr16:24351771
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0223 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.296-3062A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351771 | ||||||
| chr16:24351814
|
A | G | 95 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.296-3019A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351814 | ||||||
| chr16:24351831
|
C | CT | 6 | a0001c0001t0001g0089a0001c0001t0001g0108a0001c0001t0001g0363others(3): Show | 6 | HG01346.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-2981dupT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351831 | |||||
| chr16:24351831
|
CT | C | 94 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0030others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.296-2981delT | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351831 | |||||
| chr16:24351831
|
CTT | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 200 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.296-2982_296-2981d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351831 | |||||
| chr16:24351831
|
CTTT | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0058others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.296-2983_296-2981d others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24351831 | |||||
| chr16:24351832
|
T | TC | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(12): Show | 15 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-3001_296-3000i others(3): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351832 | ||||||
| chr16:24351833
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.296-3000T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24351833 | ||||||
| chr16:24352049
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.296-2784C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352049 | ||||||
| chr16:24352091
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.296-2742T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352091 | ||||||
| chr16:24352115
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.296-2718G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352115 | ||||||
| chr16:24352185
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.296-2648A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352185 | ||||||
| chr16:24352194
|
G | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(14): Show | 17 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-2639G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352194 | ||||||
| chr16:24352311
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0093others(16): Show | 19 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.296-2522C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352311 | ||||||
| chr16:24352436
|
A | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.296-2397A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352436 | ||||||
| chr16:24352447
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.296-2386C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352447 | ||||||
| chr16:24352448
|
A | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-2385A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352448 | ||||||
| chr16:24352451
|
G | A | 32 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0036others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.296-2382G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352451 | ||||||
| chr16:24352458
|
C | T | 95 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.296-2375C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352458 | ||||||
| chr16:24352476
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.296-2357G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352476 | ||||||
| chr16:24352521
|
T | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.296-2312T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352521 | ||||||
| chr16:24352530
|
GTTGT | G | 117 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0033others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.296-2279_296-2276d others(6): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24352530 | |||||
| chr16:24352530
|
GTTGTTTG others(1): Show |
G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.296-2283_296-2276d others(10): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24352530 | |||||
| chr16:24352547
|
TTG | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(14): Show | 17 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-2284_296-2283d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 24352547 | |||||
| chr16:24352652
|
C | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(12): Show | 15 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-2181C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352652 | ||||||
| chr16:24352894
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0206 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.296-1939C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352894 | ||||||
| chr16:24352926
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.296-1907A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352926 | ||||||
| chr16:24352967
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0099others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-1866G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24352967 | ||||||
| chr16:24353061
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.296-1772C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353061 | ||||||
| chr16:24353086
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.296-1747C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353086 | ||||||
| chr16:24353099
|
T | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0002g0310others(2): Show | 5 | HG02622.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-1734T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353099 | ||||||
| chr16:24353131
|
A | G | 177 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.296-1702A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353131 | ||||||
| chr16:24353196
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.296-1637A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353196 | ||||||
| chr16:24353242
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-1591T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353242 | ||||||
| chr16:24353293
|
T | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0049others(35): Show | 38 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.296-1540T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353293 | ||||||
| chr16:24353318
|
C | A | 320 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.296-1515C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353318 | ||||||
| chr16:24353323
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0269others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-1510G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353323 | ||||||
| chr16:24353370
|
C | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0241 | 2 | NA18946.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.296-1463C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353370 | ||||||
| chr16:24353385
|
T | C | 32 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0061others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.296-1448T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353385 | ||||||
| chr16:24353393
|
T | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0223a0001c0001t0001g0291 | 3 | HG02615.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.296-1440T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353393 | ||||||
| chr16:24353437
|
C | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0313a0001c0001t0002g0283 | 3 | HG00140.hp2 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.296-1396C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353437 | ||||||
| chr16:24353569
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0254 | 2 | HG02148.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.296-1264T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353569 | ||||||
| chr16:24353617
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0062others(4): Show | 7 | HG00423.hp2 HG02027.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-1216G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353617 | ||||||
| chr16:24353659
|
C | T | 91 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(88): Show | 91 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.296-1174C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353659 | ||||||
| chr16:24353667
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0092others(13): Show | 16 | HG01361.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.296-1166C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353667 | ||||||
| chr16:24353793
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0092others(16): Show | 19 | HG01361.hp2 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.296-1040G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353793 | ||||||
| chr16:24353928
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0206 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.296-905C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24353928 | ||||||
| chr16:24354151
|
C | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0223 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.296-682C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354151 | ||||||
| chr16:24354154
|
T | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0236 | 3 | HG01070.hp1 HG01071.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.296-679T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354154 | ||||||
| chr16:24354245
|
T | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.296-588T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354245 | ||||||
| chr16:24354374
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0002g0320a0001c0002t0001g0190 | 3 | HG00733.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.296-459C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354374 | ||||||
| chr16:24354391
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0128others(3): Show | 6 | HG00642.hp2 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-442G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354391 | ||||||
| chr16:24354450
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-383G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354450 | ||||||
| chr16:24354754
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.296-79A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354754 | ||||||
| chr16:24354757
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0223 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.296-76C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354757 | ||||||
| chr16:24354783
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.296-50C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 2/3 | chr16 | 24354783 | ||||||
| chr16:24355072
|
G | T | 1 | a0001c0001t0002g0067 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436+99G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355072 | ||||||
| chr16:24355168
|
GA | G | 44 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0055others(41): Show | 44 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.436+200delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24355168 | |||||
| chr16:24355187
|
G | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0001t0005g0008 | 3 | NA18962.hp1 NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.436+214G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355187 | ||||||
| chr16:24355195
|
C | G | 46 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0042others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.436+222C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355195 | ||||||
| chr16:24355204
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.436+231G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355204 | ||||||
| chr16:24355220
|
G | A | 1 | a0001c0001t0001g0357 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436+247G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355220 | ||||||
| chr16:24355273
|
TAA | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0106a0001c0001t0001g0107others(8): Show | 11 | HG00738.hp2 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.436+301_436+302del others(2): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355273 | ||||||
| chr16:24355318
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.436+345G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355318 | ||||||
| chr16:24355332
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.436+359G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355332 | ||||||
| chr16:24355365
|
G | A | 1 | a0001c0001t0001g0349 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.436+392G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355365 | ||||||
| chr16:24355371
|
C | T | 3 | a0001c0001t0001g0321a0001c0001t0002g0068a0001c0001t0002g0171 | 3 | HG02735.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.436+398C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355371 | ||||||
| chr16:24355379
|
G | GC | 345 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(342): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.436+407dupC | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24355379 | |||||
| chr16:24355492
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.436+519G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355492 | ||||||
| chr16:24355518
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.436+545G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355518 | ||||||
| chr16:24355564
|
C | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0088others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+591C>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355564 | ||||||
| chr16:24355641
|
A | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(101): Show | 104 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.436+668A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355641 | ||||||
| chr16:24355650
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.436+677T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355650 | ||||||
| chr16:24355651
|
A | G | 1 | a0001c0001t0003g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.436+678A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355651 | ||||||
| chr16:24355688
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.436+715A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355688 | ||||||
| chr16:24355753
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.436+780A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24355753 | ||||||
| chr16:24356202
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436+1229G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356202 | ||||||
| chr16:24356256
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0001g0161a0001c0001t0001g0181others(10): Show | 13 | HG00733.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.436+1283G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356256 | ||||||
| chr16:24356264
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.436+1291C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356264 | ||||||
| chr16:24356267
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.436+1294C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356267 | ||||||
| chr16:24356270
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.436+1297T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356270 | ||||||
| chr16:24356271
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.436+1298G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356271 | ||||||
| chr16:24356416
|
C | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.436+1443C>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356416 | ||||||
| chr16:24356419
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(171): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.436+1446C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356419 | ||||||
| chr16:24356433
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.436+1460G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356433 | ||||||
| chr16:24356516
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.436+1543A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356516 | ||||||
| chr16:24356623
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.436+1650G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356623 | ||||||
| chr16:24356887
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.436+1914C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356887 | ||||||
| chr16:24356974
|
T | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(152): Show | 155 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.436+2001T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24356974 | ||||||
| chr16:24357000
|
G | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0209a0001c0001t0001g0223others(1): Show | 4 | HG02970.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2027G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357000 | ||||||
| chr16:24357128
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.436+2155G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357128 | ||||||
| chr16:24357232
|
TA | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0140a0001c0001t0001g0161others(4): Show | 7 | HG01069.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+2280delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24357232 | |||||
| chr16:24357232
|
TAA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.436+2279_436+2280d others(4): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24357232 | |||||
| chr16:24357232
|
TAAA | T | 93 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.436+2278_436+2280d others(5): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24357232 | |||||
| chr16:24357408
|
T | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0037others(54): Show | 57 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.436+2435T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357408 | ||||||
| chr16:24357475
|
T | C | 107 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0021others(104): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.436+2502T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357475 | ||||||
| chr16:24357486
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.436+2513G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357486 | ||||||
| chr16:24357528
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0032others(81): Show | 84 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.436+2555G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357528 | ||||||
| chr16:24357532
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.436+2559G>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357532 | ||||||
| chr16:24357755
|
T | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0021others(99): Show | 102 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.436+2782T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357755 | ||||||
| chr16:24357761
|
G | A | 20 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0084others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.436+2788G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357761 | ||||||
| chr16:24357805
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0137others(9): Show | 12 | HG01361.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.436+2832T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357805 | ||||||
| chr16:24357818
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.436+2845T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357818 | ||||||
| chr16:24357858
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.436+2885T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24357858 | ||||||
| chr16:24358127
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0157a0001c0001t0001g0161others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3154T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358127 | ||||||
| chr16:24358183
|
G | GA | 9 | a0001c0001t0001g0092a0001c0001t0001g0157a0001c0001t0001g0161others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.437-3163dupA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24358183 | |||||
| chr16:24358473
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-2879C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358473 | ||||||
| chr16:24358583
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-2769G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358583 | ||||||
| chr16:24358592
|
T | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0161a0001c0001t0001g0189others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-2760T>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358592 | ||||||
| chr16:24358741
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0058a0001c0001t0001g0095others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.437-2611G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358741 | ||||||
| chr16:24358759
|
AC | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0319a0001c0001t0002g0251others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-2591delC | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24358759 | |||||
| chr16:24358930
|
G | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0032others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.437-2422G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24358930 | ||||||
| chr16:24359013
|
A | C | 38 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0061others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.437-2339A>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359013 | ||||||
| chr16:24359066
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0002g0045 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.437-2286G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359066 | ||||||
| chr16:24359165
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0113 | 2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.437-2187C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359165 | ||||||
| chr16:24359213
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-2139C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359213 | ||||||
| chr16:24359214
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.437-2138G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359214 | ||||||
| chr16:24359248
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0174a0001c0001t0001g0301others(1): Show | 4 | HG03831.hp2 HG04228.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-2104T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359248 | ||||||
| chr16:24359360
|
T | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0019others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.437-1992T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359360 | ||||||
| chr16:24359803
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0161a0001c0001t0001g0189others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-1549C>T | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359803 | ||||||
| chr16:24359857
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.437-1495T>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24359857 | ||||||
| chr16:24359864
|
AAAAAC | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0061others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.437-1469_437-1465d others(7): Show |
CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24359864 | |||||
| chr16:24360002
|
G | C | 5 | a0001c0001t0001g0194a0001c0001t0001g0299a0001c0001t0003g0127others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-1350G>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24360002 | ||||||
| chr16:24360247
|
CA | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(235): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.437-1096delA | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 24360247 | |||||
| chr16:24360533
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.437-819G>A | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24360533 | ||||||
| chr16:24360541
|
T | C | 5 | a0001c0001t0001g0194a0001c0001t0001g0299a0001c0001t0003g0127others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-811T>C | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24360541 | ||||||
| chr16:24360673
|
A | G | 4 | a0001c0001t0001g0089a0001c0001t0001g0195a0001c0001t0001g0319others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-679A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24360673 | ||||||
| chr16:24360828
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.437-524A>G | CACNG3 | ENSG00000006116.4 | transcript | ENST00000005284.4 | protein_coding | 3/3 | chr16 | 24360828 |