geneid | 27092 |
---|---|
ensemblid | ENSG00000075461.6 |
hgncid | 1408 |
symbol | CACNG4 |
name | calcium voltage-gated channel auxiliary subunit gamma 4 |
refseq_nuc | NM_014405.4 |
refseq_prot | NP_055220.1 |
ensembl_nuc | ENST00000262138.4 |
ensembl_prot | ENSP00000262138.3 |
mane_status | MANE Select |
chr | chr17 |
start | 66964707 |
end | 67033398 |
strand | + |
ver | v1.2 |
region | chr17:66964707-67033398 |
region5000 | chr17:66959707-67038398 |
regionname0 | CACNG4_chr17_66964707_67033398 |
regionname5000 | CACNG4_chr17_66959707_67038398 |
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 | 327 | 349 | 91 | 74 | 136 | 8 | 38 | 96 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0002 | 0/0 | 327 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
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 | 984 | 305 | 87 | 60 | 117 | 7 | 32 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
c0002 | 0/0 | 984 | 32 | 1 | 12 | 17 | 1 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
c0003 | 0/0 | 984 | 9 | 0 | 2 | 2 | 0 | 5 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
c0004 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
c0005 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2600 | 104 | 4 | 14 | 71 | 3 | 11 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0002 | 1/0 | 2600 | 89 | 28 | 30 | 17 | 1 | 12 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0003 | 0/0 | 2600 | 60 | 14 | 13 | 23 | 3 | 7 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0004 | 0/0 | 2600 | 18 | 2 | 2 | 12 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0005 | 0/0 | 2600 | 13 | 12 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0006 | 0/0 | 2600 | 8 | 7 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0007 | 0/0 | 2600 | 6 | 0 | 1 | 5 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0008 | 0/0 | 2600 | 6 | 3 | 3 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0009 | 0/0 | 2600 | 3 | 0 | 2 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0010 | 0/0 | 2600 | 3 | 0 | 0 | 3 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0011 | 0/0 | 2600 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0012 | 0/0 | 2600 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0013 | 0/0 | 2600 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0014 | 0/0 | 2600 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0015 | 0/0 | 2600 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0016 | 0/0 | 2600 | 2 | 0 | 0 | 0 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0017 | 0/0 | 2600 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0018 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0019 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0020 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0021 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0022 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0023 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0024 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0025 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0026 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0027 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0028 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0029 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0030 | 0/0 | 2600 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0031 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0032 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0033 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0034 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0035 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0036 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0037 | 0/0 | 2600 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0038 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0039 | 0/0 | 2600 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0040 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0041 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0042 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
t0043 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
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 | 984 | 305 | 87 | 60 | 117 | 7 | 32 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0002 | 0/0 | 984 | 32 | 1 | 12 | 17 | 1 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0003 | 0/0 | 984 | 9 | 0 | 2 | 2 | 0 | 5 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0005 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0002c0004 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3583 | 101 | 3 | 14 | 70 | 3 | 10 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0002 | 1/0 | 3583 | 55 | 24 | 17 | 2 | 0 | 11 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0003 | 0/0 | 3583 | 55 | 13 | 13 | 22 | 3 | 4 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0004 | 0/0 | 3583 | 18 | 2 | 2 | 12 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0005 | 0/0 | 3583 | 12 | 11 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0006 | 0/0 | 3583 | 8 | 7 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0007 | 0/0 | 3583 | 5 | 0 | 0 | 5 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0008 | 0/0 | 3583 | 6 | 3 | 3 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0009 | 0/0 | 3583 | 3 | 0 | 2 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0010 | 0/0 | 3583 | 3 | 0 | 0 | 3 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0011 | 0/0 | 3583 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0012 | 0/0 | 3583 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0013 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0014 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0015 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0016 | 0/0 | 3583 | 2 | 0 | 0 | 0 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0017 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0019 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0020 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0021 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0023 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0024 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0025 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0026 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0027 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0028 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0029 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0030 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0031 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0032 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0033 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0034 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0035 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0037 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0038 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0039 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0040 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0041 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0042 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0001t0043 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0002t0002 | 0/0 | 3583 | 29 | 1 | 11 | 15 | 1 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0002t0007 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0002t0022 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0002t0036 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0003t0001 | 0/0 | 3583 | 2 | 0 | 0 | 1 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0003t0002 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0003t0003 | 0/0 | 3583 | 4 | 0 | 0 | 1 | 0 | 3 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0003t0018 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0005t0002 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0001c0005t0005 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0002c0004t0001 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0002c0004t0002 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
a0002c0004t0003 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | copy fasta | chr17 | 66959707 | 67038398 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0009g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0011g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0013g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0013g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0014g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0015g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0015g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0016g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0017g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0019g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0020g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0021g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0023g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0024g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0025g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0028g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0029g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0030g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0031g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0032g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0033g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0034g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0035g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0037g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0038g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0039g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0040g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0041g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0042g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0001t0043g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0022g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0002t0036g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0003t0018g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0005t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0005t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0001c0005t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0002c0004t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0002c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
a0002c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0342 | EUR | GBR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0255 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0257 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00741 | hp1 | a0001 | c0001 | t0015 | g0302 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0330 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01099 | hp1 | a0001 | c0001 | t0039 | g0124 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01099 | hp2 | a0001 | c0001 | t0013 | g0236 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0123 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0242 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0250 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0308 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0251 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01243 | hp2 | a0001 | c0001 | t0037 | g0232 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0327 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01361 | hp2 | a0001 | c0001 | t0030 | g0183 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0258 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01517 | hp1 | a0001 | c0001 | t0031 | g0303 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01891 | hp2 | a0001 | c0001 | t0023 | g0267 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0320 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01978 | hp2 | a0001 | c0002 | t0007 | g0256 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0322 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02027 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02055 | hp1 | a0002 | c0004 | t0003 | g0271 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02165 | hp1 | a0001 | c0003 | t0003 | g0159 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02257 | hp2 | a0002 | c0004 | t0001 | g0272 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0076 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02451 | hp1 | a0001 | c0001 | t0017 | g0172 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02602 | hp2 | a0001 | c0003 | t0003 | g0091 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02622 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02647 | hp1 | a0001 | c0001 | t0040 | g0274 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02683 | hp2 | a0001 | c0001 | t0016 | g0307 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0344 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0190 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02723 | hp2 | a0001 | c0001 | t0033 | g0050 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02735 | hp1 | a0001 | c0001 | t0027 | g0175 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02809 | hp1 | a0001 | c0001 | t0021 | g0244 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0301 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02922 | hp2 | a0001 | c0005 | t0002 | g0029 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0199 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02970 | hp1 | a0001 | c0001 | t0035 | g0188 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0343 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0246 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03139 | hp2 | a0001 | c0001 | t0042 | g0060 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03195 | hp2 | a0001 | c0001 | t0017 | g0059 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03225 | hp1 | a0001 | c0001 | t0026 | g0205 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0290 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03540 | hp2 | a0001 | c0001 | t0038 | g0169 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03654 | hp1 | a0001 | c0001 | t0024 | g0210 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03654 | hp2 | a0001 | c0003 | t0018 | g0259 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03688 | hp1 | a0001 | c0001 | t0016 | g0100 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0071 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03710 | hp2 | a0001 | c0003 | t0003 | g0107 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03834 | hp2 | a0001 | c0001 | t0025 | g0222 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0106 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0247 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18522 | hp2 | a0001 | c0001 | t0032 | g0316 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18959 | hp1 | a0001 | c0001 | t0010 | g0278 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18965 | hp2 | a0001 | c0002 | t0036 | g0293 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18966 | hp1 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18982 | hp2 | a0001 | c0001 | t0007 | g0253 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19055 | hp2 | a0001 | c0002 | t0022 | g0090 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19067 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19074 | hp2 | a0001 | c0001 | t0028 | g0148 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19086 | hp1 | a0001 | c0001 | t0029 | g0053 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA19240 | hp2 | a0001 | c0005 | t0005 | g0030 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ASW | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ASW | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | TSI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02486 | hp2 | a0001 | c0001 | t0034 | g0189 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02559 | hp1 | a0001 | c0001 | t0041 | g0155 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG02559 | hp2 | a0002 | c0004 | t0002 | g0234 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0340 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA20300 | hp2 | a0001 | c0005 | t0002 | g0031 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA21309 | hp1 | a0001 | c0001 | t0043 | g0171 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0310 | REF | REF | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67024880
|
G | A | 1 | a0002 | 3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.325G>A | p.Val109Ile | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/4 | 530/3583 | 325/984 | 109/327 | chr17 | 67024880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67018244
|
C | T | 1 | a0001c0003 | 9 | HG00408.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
synonymous_variant | LOW | c.276C>T | p.Tyr92Tyr | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/4 | 481/3583 | 276/984 | 92/327 | chr17 | 67018244 | ||
chr17:67024909
|
C | T | 1 | a0001c0005 | 3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.354C>T | p.Leu118Leu | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/4 | 559/3583 | 354/984 | 118/327 | chr17 | 67024909 | ||
chr17:67030770
|
C | T | 1 | a0001c0002 | 32 | HG00140.hp2 HG00609.hp1 HG00738.hp2 others(29): Show |
synonymous_variant | LOW | c.750C>T | p.Thr250Thr | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 955/3583 | 750/984 | 250/327 | chr17 | 67030770 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:66964745
|
C | G | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 167 | chr17 | 66964745 | |||||
chr17:66964771
|
G | A | 5 | a0001c0001t0007a0001c0001t0009a0001c0001t0013others(2): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-141G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 141 | chr17 | 66964771 | |||||
chr17:66964774
|
G | C | 5 | a0001c0001t0006a0001c0001t0014a0001c0001t0019others(2): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 138 | chr17 | 66964774 | |||||
chr17:66964783
|
C | T | 4 | a0001c0001t0012a0001c0001t0017a0001c0001t0041others(1): Show | 7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 129 | chr17 | 66964783 | |||||
chr17:67031018
|
T | A | 1 | a0001c0002t0022 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 14 | chr17 | 67031018 | |||||
chr17:67031025
|
G | A | 1 | a0001c0001t0023 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 21 | chr17 | 67031025 | |||||
chr17:67031177
|
G | A | 1 | a0001c0001t0024 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 173 | chr17 | 67031177 | |||||
chr17:67031226
|
A | T | 2 | a0001c0001t0011a0001c0001t0040 | 4 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*222A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 222 | chr17 | 67031226 | |||||
chr17:67031266
|
C | T | 2 | a0001c0001t0017a0001c0001t0039 | 3 | HG01099.hp1 HG02451.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*262C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 262 | chr17 | 67031266 | |||||
chr17:67031392
|
T | C | 1 | a0001c0001t0025 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 388 | chr17 | 67031392 | |||||
chr17:67031424
|
C | T | 2 | a0001c0001t0021a0001c0001t0038 | 2 | HG02809.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 420 | chr17 | 67031424 | |||||
chr17:67031425
|
G | A | 1 | a0001c0001t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 421 | chr17 | 67031425 | |||||
chr17:67031440
|
G | A | 1 | a0001c0001t0015 | 2 | HG00741.hp1 HG01168.hp2 |
3_prime_UTR_variant | MODIFIER | c.*436G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 436 | chr17 | 67031440 | |||||
chr17:67031488
|
G | A | 2 | a0001c0001t0017a0001c0001t0039 | 3 | HG01099.hp1 HG02451.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*484G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 484 | chr17 | 67031488 | |||||
chr17:67031510
|
C | G | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0020others(6): Show | 22 | HG01243.hp2 HG01346.hp2 HG01884.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*506C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 506 | chr17 | 67031510 | |||||
chr17:67031624
|
G | C | 12 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(9): Show | 120 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*620G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 620 | chr17 | 67031624 | |||||
chr17:67031652
|
C | T | 1 | a0001c0001t0040 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 648 | chr17 | 67031652 | |||||
chr17:67031821
|
C | A | 1 | a0001c0001t0030 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 817 | chr17 | 67031821 | |||||
chr17:67031879
|
G | A | 1 | a0001c0001t0010 | 3 | NA18959.hp1 NA18990.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*875G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 875 | chr17 | 67031879 | |||||
chr17:67031969
|
C | T | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 965 | chr17 | 67031969 | |||||
chr17:67032172
|
C | T | 1 | a0001c0002t0036 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1168C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1168 | chr17 | 67032172 | |||||
chr17:67032178
|
G | A | 2 | a0001c0001t0008a0001c0001t0014 | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1174G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1174 | chr17 | 67032178 | |||||
chr17:67032534
|
C | T | 2 | a0001c0001t0012a0001c0001t0035 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1530C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1530 | chr17 | 67032534 | |||||
chr17:67032624
|
G | A | 1 | a0001c0001t0031 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1620 | chr17 | 67032624 | |||||
chr17:67032649
|
G | A | 1 | a0001c0001t0027 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1645 | chr17 | 67032649 | |||||
chr17:67032683
|
C | T | 1 | a0001c0001t0029 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1679 | chr17 | 67032683 | |||||
chr17:67032783
|
C | T | 1 | a0001c0001t0034 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1779C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1779 | chr17 | 67032783 | |||||
chr17:67032936
|
C | T | 7 | a0001c0001t0003a0001c0001t0013a0001c0001t0019others(4): Show | 65 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1932C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1932 | chr17 | 67032936 | |||||
chr17:67032948
|
C | T | 1 | a0001c0001t0016 | 2 | HG02683.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1944C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1944 | chr17 | 67032948 | |||||
chr17:67033062
|
C | G | 1 | a0001c0001t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2058 | chr17 | 67033062 | |||||
chr17:67033123
|
C | T | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2119C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2119 | chr17 | 67033123 | |||||
chr17:67033148
|
C | T | 2 | a0001c0001t0004a0001c0001t0009 | 21 | HG00609.hp2 HG01069.hp1 HG01106.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2144C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2144 | chr17 | 67033148 | |||||
chr17:67033336
|
C | G | 1 | a0001c0001t0028 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2332C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2332 | chr17 | 67033336 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:66965157
|
GCC | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0162others(41): Show | 45 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.220+29_220+30delCC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965157 | |||||
chr17:66965158
|
C | CCA | 31 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(28): Show | 31 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
C | CCACA | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 14 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
C | CCACACA | 10 | a0001c0001t0001g0012a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00609.hp2 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
C | CCACACAC others(1): Show |
72 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0094others(69): Show | 73 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
C | CCACACAC others(3): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(14): Show | 17 | HG01070.hp1 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0003g0018a0001c0001t0012g0019 | 2 | HG02647.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.220+28_220+29insAC others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965158
|
CCCCACAC others(3): Show |
C | 5 | a0001c0001t0003g0005a0001c0001t0003g0233a0001c0001t0003g0235others(2): Show | 6 | HG01243.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+29_220+38delCC others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | |||||
chr17:66965160
|
C | A | 183 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(180): Show | 186 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.220+29C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965160 | ||||||
chr17:66965160
|
C | CCA | 17 | a0001c0001t0001g0265a0001c0001t0002g0264a0001c0001t0003g0266others(14): Show | 17 | HG00438.hp1 HG00597.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.220+54_220+55dupCA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | |||||
chr17:66965160
|
C | CCACA | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(3): Show | 6 | HG01099.hp2 HG02027.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+52_220+55dupCA others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | |||||
chr17:66965160
|
C | CCACACA | 12 | a0001c0001t0002g0238a0001c0001t0006g0239a0001c0001t0006g0240others(9): Show | 12 | HG01109.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+50_220+55dupCA others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | |||||
chr17:66965162
|
A | C | 2 | a0001c0001t0005g0343a0001c0001t0011g0344 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+31A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965162 | ||||||
chr17:66965176
|
ACACACAC others(29): Show |
A | 1 | a0001c0001t0003g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.220+56_220+91delTA others(34): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965176 | |||||
chr17:66965177
|
CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0003g0229 | 3 | NA19004.hp2 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.220+53_220+64delAC others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965177 | |||||
chr17:66965180
|
ACACACAT others(25): Show |
A | 1 | a0001c0001t0003g0156 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220+56_220+87delTA others(30): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965180 | |||||
chr17:66965184
|
ACATATAC others(21): Show |
A | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+56_220+83delTA others(26): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965184 | |||||
chr17:66965185
|
C | CACAT | 5 | a0001c0001t0001g0187a0001c0001t0002g0185a0001c0001t0002g0186others(2): Show | 5 | HG02486.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+55_220+56insCA others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965185 | |||||
chr17:66965187
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(120): Show | 126 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.220+56T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965187 | ||||||
chr17:66965189
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(162): Show | 169 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.220+58T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965189 | ||||||
chr17:66965191
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.220+60C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965191 | ||||||
chr17:66965194
|
ACG | A | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+81_220+82delGC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965194 | |||||
chr17:66965194
|
ACGCGCGC others(11): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.220+65_220+82delGC others(16): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965194 | |||||
chr17:66965196
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+65G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965196 | ||||||
chr17:66965197
|
C | T | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+66C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965197 | ||||||
chr17:66965198
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+67G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965198 | ||||||
chr17:66965200
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+69G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965200 | ||||||
chr17:66965202
|
G | A | 4 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+71G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965202 | ||||||
chr17:66965204
|
G | A | 4 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+73G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965204 | ||||||
chr17:66965210
|
G | A | 6 | a0001c0001t0001g0187a0001c0001t0002g0185a0001c0001t0002g0186others(3): Show | 6 | HG02486.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+79G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965210 | ||||||
chr17:66965212
|
G | A | 8 | a0001c0001t0001g0187a0001c0001t0002g0185a0001c0001t0002g0186others(5): Show | 8 | HG00609.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+81G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965212 | ||||||
chr17:66965212
|
G | GCA | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00544.hp2 HG00621.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.220+93_220+94dupAC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | |||||
chr17:66965212
|
G | GCGCA | 23 | a0001c0001t0001g0045a0001c0001t0001g0070a0001c0001t0001g0073others(20): Show | 24 | HG00741.hp2 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.220+82_220+83insGC others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | |||||
chr17:66965212
|
G | GCGCGCA | 6 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0161others(3): Show | 7 | HG02040.hp2 HG03209.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+82_220+83insGC others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | |||||
chr17:66965217
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.220+86C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965217 | ||||||
chr17:66965222
|
A | G | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+91A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965222 | ||||||
chr17:66965224
|
A | G | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+93A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965224 | ||||||
chr17:66965549
|
G | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG02109.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.220+418G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965549 | ||||||
chr17:66965554
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0003g0154 | 2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+423G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965554 | ||||||
chr17:66965595
|
T | C | 5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+464T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965595 | ||||||
chr17:66965791
|
C | T | 9 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(6): Show | 9 | HG00438.hp1 HG00597.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+660C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965791 | ||||||
chr17:66965846
|
G | T | 1 | a0001c0001t0004g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.220+715G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965846 | ||||||
chr17:66965850
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.220+719T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965850 | ||||||
chr17:66966002
|
T | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(99): Show | 104 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.220+871T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966002 | ||||||
chr17:66966066
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+935T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966066 | ||||||
chr17:66966102
|
C | G | 1 | a0001c0001t0004g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.220+971C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966102 | ||||||
chr17:66966108
|
C | G | 12 | a0001c0001t0006g0239a0001c0001t0006g0240a0001c0001t0006g0241others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+977C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966108 | ||||||
chr17:66966295
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220+1164G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966295 | ||||||
chr17:66966409
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220+1278T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966409 | ||||||
chr17:66966414
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.220+1283G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966414 | ||||||
chr17:66966438
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.220+1307C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966438 | ||||||
chr17:66966476
|
C | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+1345C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966476 | ||||||
chr17:66966857
|
T | A | 2 | a0001c0001t0003g0194a0001c0002t0002g0193 | 2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.220+1726T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966857 | ||||||
chr17:66966876
|
T | C | 4 | a0001c0001t0003g0181a0001c0001t0005g0182a0001c0001t0011g0190others(1): Show | 4 | HG01361.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1745T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966876 | ||||||
chr17:66967046
|
C | T | 1 | a0001c0001t0043g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220+1915C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967046 | ||||||
chr17:66967311
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0002g0340a0001c0002t0002g0342 | 3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+2180A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967311 | ||||||
chr17:66967342
|
T | G | 4 | a0001c0001t0003g0181a0001c0001t0005g0182a0001c0001t0011g0190others(1): Show | 4 | HG01361.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+2211T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967342 | ||||||
chr17:66967347
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(11): Show | 15 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.220+2216G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967347 | ||||||
chr17:66967435
|
C | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+2304C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967435 | ||||||
chr17:66967573
|
G | A | 1 | a0001c0001t0001g0006 | 2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.220+2442G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967573 | ||||||
chr17:66967582
|
G | T | 1 | a0001c0001t0003g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.220+2451G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967582 | ||||||
chr17:66967653
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.220+2522C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967653 | ||||||
chr17:66967817
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220+2686G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967817 | ||||||
chr17:66968007
|
C | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.220+2876C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968007 | ||||||
chr17:66968165
|
G | A | 12 | a0001c0001t0006g0239a0001c0001t0006g0240a0001c0001t0006g0241others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+3034G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968165 | ||||||
chr17:66968358
|
C | T | 1 | a0001c0001t0006g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220+3227C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968358 | ||||||
chr17:66968359
|
G | A | 3 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236 | 3 | HG01099.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.220+3228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968359 | ||||||
chr17:66968500
|
C | G | 4 | a0001c0001t0001g0149a0001c0001t0003g0058a0001c0001t0003g0150others(1): Show | 4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3369C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968500 | ||||||
chr17:66968514
|
A | C | 4 | a0001c0001t0001g0149a0001c0001t0003g0058a0001c0001t0003g0150others(1): Show | 4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3383A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968514 | ||||||
chr17:66968517
|
C | T | 2 | a0001c0001t0005g0343a0001c0001t0011g0344 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+3386C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968517 | ||||||
chr17:66968518
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3387T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968518 | ||||||
chr17:66968519
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3388C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968519 | ||||||
chr17:66968527
|
G | C | 4 | a0001c0001t0001g0149a0001c0001t0003g0058a0001c0001t0003g0150others(1): Show | 4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3396G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968527 | ||||||
chr17:66968527
|
G | GCCTCCTC others(101): Show |
6 | a0001c0001t0002g0264a0001c0001t0003g0266a0001c0001t0003g0268others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+3437_220+3544d others(110): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | |||||
chr17:66968527
|
GCCTCCTC others(47): Show |
G | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146 | 3 | HG03490.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.220+3437_220+3490d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | |||||
chr17:66968527
|
GCCTCCTC others(74): Show |
G | 1 | a0001c0001t0005g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.220+3437_220+3517d others(83): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | |||||
chr17:66968541
|
CCCCTCCT others(20): Show |
C | 3 | a0001c0001t0001g0143a0001c0001t0002g0142a0001c0001t0013g0258 | 3 | HG01496.hp2 HG02523.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.220+3437_220+3463d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968541 | |||||
chr17:66968550
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+3419C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968550 | ||||||
chr17:66968564
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3433C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968564 | ||||||
chr17:66968567
|
T | C | 2 | a0001c0001t0003g0058a0001c0001t0003g0068 | 2 | HG01257.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.220+3436T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968567 | ||||||
chr17:66968568
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(169): Show | 177 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.220+3437T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968568 | ||||||
chr17:66968568
|
T | TCCCTCCT others(20): Show |
1 | a0001c0001t0002g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220+3542_220+3568d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | |||||
chr17:66968568
|
TCCCTCCT others(20): Show |
T | 1 | a0001c0001t0003g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.220+3542_220+3568d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | |||||
chr17:66968568
|
TCCCTCCT others(47): Show |
T | 1 | a0001c0001t0004g0339 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.220+3515_220+3568d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | |||||
chr17:66968577
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.220+3446C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968577 | ||||||
chr17:66968578
|
T | C | 1 | a0001c0001t0003g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.220+3447T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968578 | ||||||
chr17:66968623
|
CCCTCCTC others(23): Show |
C | 12 | a0001c0001t0006g0239a0001c0001t0006g0240a0001c0001t0006g0241others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+3500_220+3529d others(32): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968623 | |||||
chr17:66968650
|
CCCT | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(67): Show | 72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+3527_220+3529d others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968650 | |||||
chr17:66968808
|
C | G | 1 | a0001c0001t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220+3677C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968808 | ||||||
chr17:66968814
|
CCTCTTT | C | 6 | a0001c0001t0002g0264a0001c0001t0003g0266a0001c0001t0003g0268others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+3691_220+3696d others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968814 | |||||
chr17:66968910
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+3779T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968910 | ||||||
chr17:66969338
|
C | T | 2 | a0001c0001t0005g0178a0001c0001t0005g0179 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.220+4207C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969338 | ||||||
chr17:66969541
|
G | T | 1 | a0001c0001t0004g0338 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.220+4410G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969541 | ||||||
chr17:66969720
|
A | T | 1 | a0001c0001t0003g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220+4589A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969720 | ||||||
chr17:66969768
|
A | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(237): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+4637A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969768 | ||||||
chr17:66969831
|
T | A | 1 | a0001c0002t0002g0064 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.220+4700T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969831 | ||||||
chr17:66969876
|
T | C | 1 | a0001c0001t0011g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+4745T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969876 | ||||||
chr17:66969957
|
G | T | 15 | a0001c0001t0003g0181a0001c0001t0005g0182a0001c0001t0006g0239others(12): Show | 16 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+4826G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969957 | ||||||
chr17:66969982
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0005g0177 | 2 | HG03098.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.220+4851C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969982 | ||||||
chr17:66969985
|
G | A | 2 | a0001c0001t0005g0343a0001c0001t0011g0344 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+4854G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969985 | ||||||
chr17:66969998
|
G | A | 1 | a0001c0001t0011g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+4867G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969998 | ||||||
chr17:66970088
|
C | T | 7 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+4957C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970088 | ||||||
chr17:66970169
|
G | A | 12 | a0001c0001t0006g0239a0001c0001t0006g0240a0001c0001t0006g0241others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+5038G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970169 | ||||||
chr17:66970193
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220+5062C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970193 | ||||||
chr17:66970328
|
G | A | 6 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(3): Show | 6 | NA18947.hp2 NA18959.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+5197G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970328 | ||||||
chr17:66970342
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.220+5211T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970342 | ||||||
chr17:66970416
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG02074.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.220+5285C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970416 | ||||||
chr17:66970811
|
C | T | 1 | a0001c0001t0003g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220+5680C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970811 | ||||||
chr17:66970839
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+5708T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970839 | ||||||
chr17:66971010
|
C | A | 1 | a0001c0002t0002g0284 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.220+5879C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971010 | ||||||
chr17:66971012
|
G | C | 12 | a0001c0001t0006g0239a0001c0001t0006g0240a0001c0001t0006g0241others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+5881G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971012 | ||||||
chr17:66971072
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0027others(4): Show | 7 | HG00558.hp1 HG00621.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+5941C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971072 | ||||||
chr17:66971114
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0285a0001c0001t0010g0278 | 3 | NA18959.hp1 NA18970.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.220+5983G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971114 | ||||||
chr17:66971127
|
C | T | 1 | a0001c0001t0034g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220+5996C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971127 | ||||||
chr17:66971160
|
C | T | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+6029C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971160 | ||||||
chr17:66971176
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 92 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220+6045A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971176 | ||||||
chr17:66971178
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 92 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220+6047A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971178 | ||||||
chr17:66971192
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 80 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.220+6061C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971192 | ||||||
chr17:66971228
|
GGAGGAGG others(22): Show |
G | 12 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(9): Show | 12 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+6157_220+6185d others(31): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66971228 | |||||
chr17:66971371
|
C | T | 2 | a0001c0001t0005g0182a0001c0001t0030g0183 | 2 | HG01361.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.220+6240C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971371 | ||||||
chr17:66971479
|
C | G | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+6348C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971479 | ||||||
chr17:66971906
|
T | G | 4 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0005g0182others(1): Show | 4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6775T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971906 | ||||||
chr17:66971932
|
T | C | 30 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(27): Show | 30 | HG00735.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.220+6801T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971932 | ||||||
chr17:66972020
|
C | G | 4 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0005g0182others(1): Show | 4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6889C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972020 | ||||||
chr17:66972097
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+6966G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972097 | ||||||
chr17:66972116
|
G | A | 4 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0005g0182others(1): Show | 4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6985G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972116 | ||||||
chr17:66972194
|
G | T | 38 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0208others(35): Show | 38 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.220+7063G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972194 | ||||||
chr17:66972226
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220+7095C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972226 | ||||||
chr17:66972358
|
C | G | 1 | a0001c0001t0002g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.220+7227C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972358 | ||||||
chr17:66972359
|
G | A | 5 | a0001c0001t0002g0289a0001c0001t0003g0288a0001c0001t0004g0286others(2): Show | 5 | HG02602.hp1 HG03490.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+7228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972359 | ||||||
chr17:66972517
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.220+7386A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972517 | ||||||
chr17:66972661
|
C | CA | 253 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(250): Show | 258 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.220+7531dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66972661 | |||||
chr17:66972734
|
T | C | 18 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(15): Show | 18 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+7603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972734 | ||||||
chr17:66972754
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(101): Show | 107 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.220+7623C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972754 | ||||||
chr17:66972831
|
C | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 70 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.220+7700C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972831 | ||||||
chr17:66972885
|
C | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(153): Show | 160 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.220+7754C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972885 | ||||||
chr17:66972924
|
TCAAAAA | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 76 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.220+7810_220+7815d others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66972924 | |||||
chr17:66972951
|
C | A | 1 | a0001c0001t0003g0058 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.220+7820C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972951 | ||||||
chr17:66972985
|
C | T | 22 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0075others(19): Show | 22 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+7854C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972985 | ||||||
chr17:66973187
|
C | T | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.220+8056C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973187 | ||||||
chr17:66973188
|
T | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(156): Show | 161 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.220+8057T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973188 | ||||||
chr17:66973197
|
G | A | 2 | a0001c0001t0003g0291a0001c0002t0002g0292 | 2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.220+8066G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973197 | ||||||
chr17:66973237
|
T | TA | 76 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.220+8121dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | |||||
chr17:66973237
|
T | TAA | 8 | a0001c0001t0002g0160a0001c0001t0002g0238a0001c0001t0003g0181others(5): Show | 8 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+8120_220+8121d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | |||||
chr17:66973237
|
TA | T | 139 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(136): Show | 141 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.220+8121delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | |||||
chr17:66973276
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.220+8145G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973276 | ||||||
chr17:66973472
|
G | A | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+8341G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973472 | ||||||
chr17:66973514
|
G | T | 2 | a0001c0001t0005g0343a0001c0001t0011g0344 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+8383G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973514 | ||||||
chr17:66973592
|
G | A | 36 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0208others(33): Show | 36 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.220+8461G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973592 | ||||||
chr17:66973620
|
C | T | 7 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+8489C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973620 | ||||||
chr17:66973699
|
G | A | 171 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(168): Show | 173 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.220+8568G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973699 | ||||||
chr17:66973749
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.220+8618G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973749 | ||||||
chr17:66973886
|
A | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(121): Show | 126 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.220+8755A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973886 | ||||||
chr17:66973909
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+8778C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973909 | ||||||
chr17:66973993
|
A | C | 1 | a0001c0001t0002g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.220+8862A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973993 | ||||||
chr17:66974406
|
G | A | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+9275G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974406 | ||||||
chr17:66974416
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(58): Show | 63 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.220+9285G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974416 | ||||||
chr17:66974595
|
G | A | 7 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+9464G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974595 | ||||||
chr17:66974707
|
C | T | 9 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0260others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+9576C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974707 | ||||||
chr17:66974749
|
A | G | 1 | a0001c0001t0043g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220+9618A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974749 | ||||||
chr17:66974820
|
T | C | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+9689T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974820 | ||||||
chr17:66975033
|
C | T | 1 | a0001c0003t0003g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.220+9902C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975033 | ||||||
chr17:66975133
|
G | A | 132 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(129): Show | 134 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.220+10002G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975133 | ||||||
chr17:66975177
|
G | T | 11 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0242others(8): Show | 12 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+10046G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975177 | ||||||
chr17:66975510
|
G | C | 1 | a0001c0001t0028g0148 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.220+10379G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975510 | ||||||
chr17:66975634
|
T | C | 7 | a0001c0001t0003g0005a0001c0001t0003g0233a0001c0001t0003g0235others(4): Show | 8 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+10503T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975634 | ||||||
chr17:66975766
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+10635G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975766 | ||||||
chr17:66975773
|
G | C | 4 | a0001c0001t0001g0283a0001c0001t0003g0296a0001c0001t0003g0297others(1): Show | 4 | HG02056.hp1 HG02293.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+10642G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975773 | ||||||
chr17:66976038
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0038g0169 | 2 | HG00735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.220+10907T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976038 | ||||||
chr17:66976082
|
G | A | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+10951G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976082 | ||||||
chr17:66976116
|
C | T | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+10985C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976116 | ||||||
chr17:66976218
|
C | T | 1 | a0001c0001t0003g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.220+11087C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976218 | ||||||
chr17:66976326
|
C | T | 22 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+11195C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976326 | ||||||
chr17:66976332
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220+11201C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976332 | ||||||
chr17:66976471
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220+11340C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976471 | ||||||
chr17:66976525
|
C | T | 3 | a0001c0001t0001g0341a0001c0001t0002g0340a0001c0002t0002g0342 | 3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+11394C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976525 | ||||||
chr17:66976577
|
TC | T | 31 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0260others(28): Show | 31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+11447delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976577 | ||||||
chr17:66976728
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.220+11597G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976728 | ||||||
chr17:66976731
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.220+11600G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976731 | ||||||
chr17:66976843
|
T | C | 105 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(102): Show | 107 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.220+11712T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976843 | ||||||
chr17:66976890
|
G | T | 9 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(6): Show | 9 | HG00438.hp1 HG00597.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+11759G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976890 | ||||||
chr17:66976953
|
A | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0049others(104): Show | 109 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.220+11822A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976953 | ||||||
chr17:66977062
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(92): Show | 98 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.220+11931C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977062 | ||||||
chr17:66977256
|
C | T | 10 | a0001c0001t0003g0005a0001c0001t0003g0235a0001c0001t0012g0019others(7): Show | 11 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+12125C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977256 | ||||||
chr17:66977260
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 58 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.220+12129C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977260 | ||||||
chr17:66977439
|
G | C | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+12308G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977439 | ||||||
chr17:66977450
|
G | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 96 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.220+12319G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977450 | ||||||
chr17:66977797
|
C | T | 1 | a0001c0001t0011g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+12666C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977797 | ||||||
chr17:66977824
|
G | A | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+12693G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977824 | ||||||
chr17:66977861
|
T | C | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+12730T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977861 | ||||||
chr17:66977950
|
C | T | 11 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(8): Show | 11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+12819C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977950 | ||||||
chr17:66977970
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+12839C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977970 | ||||||
chr17:66978284
|
G | A | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+13153G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978284 | ||||||
chr17:66978352
|
A | G | 1 | a0001c0001t0007g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.220+13221A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978352 | ||||||
chr17:66978397
|
G | A | 3 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0269 | 3 | HG02055.hp2 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.220+13266G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978397 | ||||||
chr17:66978415
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0004g0152 | 2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.220+13284G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978415 | ||||||
chr17:66978437
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.220+13306G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978437 | ||||||
chr17:66978636
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0092others(7): Show | 10 | HG01433.hp2 HG01981.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.220+13505G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978636 | ||||||
chr17:66978711
|
G | A | 4 | a0001c0001t0003g0077a0001c0002t0002g0043a0001c0002t0002g0076others(1): Show | 4 | HG01361.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+13580G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978711 | ||||||
chr17:66978749
|
G | A | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+13618G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978749 | ||||||
chr17:66978857
|
C | T | 11 | a0001c0001t0002g0238a0001c0001t0002g0333a0001c0001t0003g0181others(8): Show | 11 | HG01361.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+13726C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978857 | ||||||
chr17:66978957
|
C | T | 1 | a0001c0001t0011g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.220+13826C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978957 | ||||||
chr17:66979010
|
C | T | 1 | a0001c0001t0004g0338 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.220+13879C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979010 | ||||||
chr17:66979050
|
G | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 95 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.220+13919G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979050 | ||||||
chr17:66979069
|
G | GTCT | 122 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(119): Show | 125 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.220+13943_220+1394 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979069 | |||||
chr17:66979167
|
C | T | 11 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(8): Show | 11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+14036C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979167 | ||||||
chr17:66979227
|
C | G | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+14096C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979227 | ||||||
chr17:66979281
|
T | A | 4 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(1): Show | 4 | HG02258.hp2 HG02717.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+14150T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979281 | ||||||
chr17:66979376
|
ACT | A | 91 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0049others(88): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.220+14248_220+1424 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979376 | |||||
chr17:66979599
|
TCTC | T | 31 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0220others(28): Show | 31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+14471_220+1447 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979599 | |||||
chr17:66979609
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(203): Show | 210 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.220+14478C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979609 | ||||||
chr17:66979613
|
C | T | 11 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0242others(8): Show | 12 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+14482C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979613 | ||||||
chr17:66979632
|
G | C | 1 | a0001c0001t0003g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220+14501G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979632 | ||||||
chr17:66979745
|
C | CT | 114 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0047others(111): Show | 116 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.220+14636dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | |||||
chr17:66979745
|
C | CTT | 65 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(62): Show | 67 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.220+14635_220+1463 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | |||||
chr17:66979745
|
C | CTTT | 7 | a0001c0001t0003g0017a0001c0001t0003g0038a0001c0001t0003g0039others(4): Show | 7 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+14634_220+1463 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | |||||
chr17:66979745
|
CT | C | 24 | a0001c0001t0001g0299a0001c0001t0002g0202a0001c0001t0002g0225others(21): Show | 25 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.220+14636delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | |||||
chr17:66979749
|
TTTTTTTT others(864): Show |
T | 1 | a0001c0002t0002g0292 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.220+14637_220+1550 others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979749 | |||||
chr17:66979829
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.220+14698A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979829 | ||||||
chr17:66979882
|
A | G | 31 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0220others(28): Show | 31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+14751A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979882 | ||||||
chr17:66979883
|
G | A | 12 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+14752G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979883 | ||||||
chr17:66979912
|
T | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0185 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.220+14781T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979912 | ||||||
chr17:66979943
|
A | T | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+14812A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979943 | ||||||
chr17:66980005
|
C | T | 81 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0049others(78): Show | 82 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.220+14874C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980005 | ||||||
chr17:66980037
|
A | G | 1 | a0001c0001t0003g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+14906A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980037 | ||||||
chr17:66980110
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.220+14979G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980110 | ||||||
chr17:66980234
|
G | T | 3 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0030g0183 | 3 | HG01361.hp2 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.220+15103G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980234 | ||||||
chr17:66980285
|
C | G | 7 | a0001c0001t0001g0096a0001c0001t0001g0149a0001c0001t0003g0058others(4): Show | 7 | HG02083.hp2 HG02165.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+15154C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980285 | ||||||
chr17:66980415
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 123 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.220+15284T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980415 | ||||||
chr17:66980416
|
G | C | 3 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0001t0008g0262 | 3 | HG02258.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.220+15285G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980416 | ||||||
chr17:66980458
|
G | A | 234 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(231): Show | 239 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.220+15327G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980458 | ||||||
chr17:66980526
|
C | A | 1 | a0001c0001t0003g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.220+15395C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980526 | ||||||
chr17:66980620
|
C | CT | 9 | a0001c0001t0001g0025a0001c0001t0002g0088a0001c0001t0002g0289others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+15509dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
C | CTTTTT | 18 | a0001c0001t0006g0239a0001c0001t0007g0253a0001c0001t0007g0254others(15): Show | 18 | HG00597.hp2 HG01099.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.220+15505_220+1550 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
C | CTTTTTT | 17 | a0001c0001t0001g0033a0001c0001t0001g0083a0001c0001t0002g0238others(14): Show | 17 | HG00438.hp1 HG01361.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+15504_220+1550 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
C | CTTTTTTT | 60 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(57): Show | 63 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.220+15503_220+1550 others(11): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
C | CTTTTTTT others(1): Show |
21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(18): Show | 21 | HG00544.hp2 HG02040.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+15502_220+1550 others(12): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
CT | C | 91 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0049others(88): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.220+15509delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980620
|
CTT | C | 9 | a0001c0001t0001g0102a0001c0001t0001g0227a0001c0001t0002g0057others(6): Show | 9 | HG01070.hp1 HG01256.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+15508_220+1550 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | |||||
chr17:66980793
|
A | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(66): Show | 72 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+15662A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980793 | ||||||
chr17:66980834
|
G | T | 1 | a0001c0001t0004g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.220+15703G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980834 | ||||||
chr17:66980909
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.220+15778G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980909 | ||||||
chr17:66981320
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.220+16189T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981320 | ||||||
chr17:66981717
|
C | G | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+16586C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981717 | ||||||
chr17:66981784
|
A | G | 3 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0030g0183 | 3 | HG01361.hp2 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.220+16653A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981784 | ||||||
chr17:66981808
|
T | C | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+16677T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981808 | ||||||
chr17:66981841
|
T | A | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+16710T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981841 | ||||||
chr17:66981855
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 59 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.220+16724A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981855 | ||||||
chr17:66981869
|
G | C | 1 | a0001c0001t0017g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.220+16738G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981869 | ||||||
chr17:66981915
|
C | G | 7 | a0001c0001t0001g0163a0001c0001t0001g0196a0001c0001t0001g0213others(4): Show | 7 | HG00621.hp2 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+16784C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981915 | ||||||
chr17:66981930
|
C | G | 1 | a0001c0002t0002g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.220+16799C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981930 | ||||||
chr17:66981945
|
A | T | 3 | a0001c0001t0001g0139a0001c0002t0002g0137a0001c0002t0002g0138 | 3 | HG00544.hp1 NA18945.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.220+16814A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981945 | ||||||
chr17:66981962
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220+16831C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981962 | ||||||
chr17:66982042
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.220+16911C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982042 | ||||||
chr17:66982063
|
G | A | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+16932G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982063 | ||||||
chr17:66982084
|
T | C | 1 | a0001c0001t0008g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220+16953T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982084 | ||||||
chr17:66982108
|
G | A | 1 | a0001c0001t0033g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220+16977G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982108 | ||||||
chr17:66982109
|
G | A | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0003g0300 | 3 | NA18942.hp1 NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.220+16978G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982109 | ||||||
chr17:66982119
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 78 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.220+16988G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982119 | ||||||
chr17:66982146
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+17015G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982146 | ||||||
chr17:66982187
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+17056C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982187 | ||||||
chr17:66982204
|
C | T | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17073C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982204 | ||||||
chr17:66982240
|
G | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0135a0001c0001t0001g0163others(13): Show | 16 | HG00621.hp2 HG01255.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+17109G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982240 | ||||||
chr17:66982249
|
CTGCTGAT others(17): Show |
C | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+17132_220+1715 others(28): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66982249 | |||||
chr17:66982273
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 115 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.220+17142A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982273 | ||||||
chr17:66982287
|
A | C | 2 | a0001c0001t0009g0250a0001c0001t0009g0251 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.220+17156A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982287 | ||||||
chr17:66982309
|
G | A | 94 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0047others(91): Show | 96 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.220+17178G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982309 | ||||||
chr17:66982339
|
C | A | 8 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+17208C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982339 | ||||||
chr17:66982403
|
T | C | 94 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0047others(91): Show | 96 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.220+17272T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982403 | ||||||
chr17:66982409
|
A | C | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17278A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982409 | ||||||
chr17:66982422
|
G | A | 8 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0103others(5): Show | 8 | HG02015.hp2 HG02040.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+17291G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982422 | ||||||
chr17:66982481
|
A | G | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+17350A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982481 | ||||||
chr17:66982508
|
GT | G | 94 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0047others(91): Show | 96 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.220+17381delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66982508 | |||||
chr17:66982599
|
G | A | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17468G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982599 | ||||||
chr17:66982793
|
C | T | 94 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0047others(91): Show | 96 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.220+17662C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982793 | ||||||
chr17:66982817
|
A | G | 1 | a0001c0002t0002g0136 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.220+17686A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982817 | ||||||
chr17:66983340
|
A | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.220+18209A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983340 | ||||||
chr17:66983368
|
G | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 217 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.220+18237G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983368 | ||||||
chr17:66983382
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.220+18251A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983382 | ||||||
chr17:66983702
|
G | T | 1 | a0001c0001t0001g0317 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.220+18571G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983702 | ||||||
chr17:66984018
|
G | A | 1 | a0001c0001t0003g0156 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220+18887G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984018 | ||||||
chr17:66984021
|
T | A | 7 | a0001c0001t0001g0104a0001c0001t0001g0328a0001c0001t0003g0068others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+18890T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984021 | ||||||
chr17:66984022
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00741.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+18891G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984022 | ||||||
chr17:66984162
|
A | C | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19031A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984162 | ||||||
chr17:66984167
|
C | T | 10 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+19036C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984167 | ||||||
chr17:66984183
|
A | AG | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19053dupG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66984183 | |||||
chr17:66984185
|
T | C | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19054T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984185 | ||||||
chr17:66984185
|
T | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 175 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.220+19054T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984185 | ||||||
chr17:66984186
|
T | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 175 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.220+19055T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984186 | ||||||
chr17:66984187
|
T | G | 43 | a0001c0001t0001g0187a0001c0001t0001g0219a0001c0001t0002g0166others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19056T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984187 | ||||||
chr17:66984259
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19128T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984259 | ||||||
chr17:66984398
|
G | T | 1 | a0001c0001t0016g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.220+19267G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984398 | ||||||
chr17:66984462
|
C | G | 6 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+19331C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984462 | ||||||
chr17:66984482
|
C | T | 1 | a0001c0001t0005g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220+19351C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984482 | ||||||
chr17:66984562
|
T | G | 1 | a0001c0001t0002g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220+19431T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984562 | ||||||
chr17:66984841
|
C | T | 2 | a0001c0002t0002g0051a0001c0002t0002g0105 | 2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.220+19710C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984841 | ||||||
chr17:66984842
|
G | T | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19711G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984842 | ||||||
chr17:66984917
|
T | C | 1 | a0001c0002t0002g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220+19786T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984917 | ||||||
chr17:66984927
|
G | A | 2 | a0001c0003t0003g0106a0001c0003t0003g0107 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.220+19796G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984927 | ||||||
chr17:66985069
|
G | A | 1 | a0001c0001t0015g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.220+19938G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985069 | ||||||
chr17:66985099
|
C | T | 1 | a0001c0001t0003g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.220+19968C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985099 | ||||||
chr17:66985231
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0092others(15): Show | 18 | HG01433.hp2 HG01981.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+20100T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985231 | ||||||
chr17:66985249
|
C | G | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+20118C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985249 | ||||||
chr17:66985256
|
C | T | 10 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+20125C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985256 | ||||||
chr17:66985374
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+20243A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985374 | ||||||
chr17:66985400
|
A | G | 12 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(9): Show | 13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.220+20269A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985400 | ||||||
chr17:66985580
|
T | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(210): Show | 218 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.220+20449T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985580 | ||||||
chr17:66985607
|
T | C | 6 | a0001c0001t0002g0035a0001c0001t0003g0017a0001c0001t0003g0034others(3): Show | 6 | HG01515.hp2 HG01517.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+20476T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985607 | ||||||
chr17:66985610
|
A | G | 12 | a0001c0001t0001g0317a0001c0001t0001g0336a0001c0001t0001g0337others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+20479A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985610 | ||||||
chr17:66985642
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220+20511A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985642 | ||||||
chr17:66985672
|
C | T | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+20541C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985672 | ||||||
chr17:66985739
|
G | A | 1 | a0001c0001t0004g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.220+20608G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985739 | ||||||
chr17:66985863
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.220+20732G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985863 | ||||||
chr17:66985943
|
GA | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.220+20822delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66985943 | |||||
chr17:66985951
|
AAAG | A | 10 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+20842_220+2084 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66985951 | |||||
chr17:66985974
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(211): Show | 219 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.220+20843A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985974 | ||||||
chr17:66985994
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.220+20863G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985994 | ||||||
chr17:66986021
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20890T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986021 | ||||||
chr17:66986022
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20891C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986022 | ||||||
chr17:66986024
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20893G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986024 | ||||||
chr17:66986506
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+21375G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986506 | ||||||
chr17:66986614
|
C | A | 2 | a0001c0001t0002g0170a0001c0001t0038g0169 | 2 | HG00735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.220+21483C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986614 | ||||||
chr17:66986976
|
C | A | 11 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(8): Show | 11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+21845C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986976 | ||||||
chr17:66987157
|
A | G | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+22026A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987157 | ||||||
chr17:66987278
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+22147C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987278 | ||||||
chr17:66987294
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0002g0340a0001c0002t0002g0342 | 3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+22163A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987294 | ||||||
chr17:66987417
|
C | A | 35 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(32): Show | 36 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.220+22286C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987417 | ||||||
chr17:66987524
|
G | C | 3 | a0001c0001t0001g0329a0001c0001t0004g0330a0001c0001t0005g0177 | 3 | HG01069.hp1 HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+22393G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987524 | ||||||
chr17:66987541
|
A | G | 1 | a0001c0001t0039g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+22410A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987541 | ||||||
chr17:66987692
|
A | G | 16 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+22561A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987692 | ||||||
chr17:66987814
|
G | A | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+22683G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987814 | ||||||
chr17:66987906
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.220+22775G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987906 | ||||||
chr17:66988029
|
T | A | 5 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0011g0190others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+22898T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988029 | ||||||
chr17:66988033
|
TTTTG | T | 9 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0017g0059others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+22904_220+2290 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988033 | |||||
chr17:66988035
|
T | G | 2 | a0001c0001t0002g0195a0001c0001t0008g0002 | 3 | HG01069.hp2 HG01071.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.220+22904T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988035 | ||||||
chr17:66988035
|
T | TTG | 5 | a0001c0001t0001g0131a0001c0001t0002g0130a0001c0001t0003g0200others(2): Show | 5 | HG01123.hp2 HG01515.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+22922_220+2292 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988035 | |||||
chr17:66988051
|
GTGTA | G | 25 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(22): Show | 26 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.220+22922_220+2292 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988051 | |||||
chr17:66988055
|
A | G | 283 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(280): Show | 288 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.220+22924A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988055 | ||||||
chr17:66988066
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220+22935T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988066 | ||||||
chr17:66988066
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0011g0344 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.220+22935T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988066 | ||||||
chr17:66988125
|
A | G | 21 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(18): Show | 21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+22994A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988125 | ||||||
chr17:66988331
|
T | C | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23200T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988331 | ||||||
chr17:66988361
|
C | T | 5 | a0001c0001t0003g0233a0001c0001t0005g0182a0001c0001t0005g0343others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+23230C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988361 | ||||||
chr17:66988365
|
G | A | 21 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(18): Show | 21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+23234G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988365 | ||||||
chr17:66988399
|
G | A | 11 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(8): Show | 11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+23268G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988399 | ||||||
chr17:66988417
|
A | T | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23286A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988417 | ||||||
chr17:66988497
|
C | T | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23366C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988497 | ||||||
chr17:66988561
|
G | A | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23430G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988561 | ||||||
chr17:66988583
|
G | A | 21 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(18): Show | 21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+23452G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988583 | ||||||
chr17:66988752
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 115 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.220+23621C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988752 | ||||||
chr17:66988760
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.220+23629G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988760 | ||||||
chr17:66988785
|
G | A | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23654G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988785 | ||||||
chr17:66988819
|
G | A | 1 | a0001c0001t0031g0303 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.220+23688G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988819 | ||||||
chr17:66988904
|
CAAAA | C | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23777_220+2378 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988904 | |||||
chr17:66989011
|
AGATCATG others(936): Show |
A | 16 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+23883_220+2482 others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989011 | |||||
chr17:66989016
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+23885A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989016 | ||||||
chr17:66989044
|
G | A | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+23913G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989044 | ||||||
chr17:66989053
|
T | A | 1 | a0001c0002t0002g0051 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.220+23922T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989053 | ||||||
chr17:66989060
|
C | CA | 122 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0028others(119): Show | 124 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.220+23950dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | |||||
chr17:66989060
|
C | CAA | 25 | a0001c0001t0001g0108a0001c0001t0003g0150a0001c0001t0006g0240others(22): Show | 26 | HG00438.hp1 HG01099.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.220+23949_220+2395 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | |||||
chr17:66989060
|
CA | C | 7 | a0001c0001t0001g0078a0001c0001t0001g0317a0001c0001t0003g0233others(4): Show | 7 | HG01517.hp1 HG02818.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+23950delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | |||||
chr17:66989084
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+23953C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989084 | ||||||
chr17:66989186
|
A | G | 8 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0260others(5): Show | 8 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+24055A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989186 | ||||||
chr17:66989209
|
C | G | 11 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(8): Show | 11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+24078C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989209 | ||||||
chr17:66989318
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+24187T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989318 | ||||||
chr17:66989453
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+24322A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989453 | ||||||
chr17:66989526
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(45): Show | 49 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.220+24395G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989526 | ||||||
chr17:66989617
|
G | A | 14 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(11): Show | 15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+24486G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989617 | ||||||
chr17:66989647
|
C | T | 14 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(11): Show | 15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+24516C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989647 | ||||||
chr17:66989660
|
C | A | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+24529C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989660 | ||||||
chr17:66989771
|
G | A | 7 | a0001c0001t0001g0055a0001c0001t0001g0126a0001c0001t0001g0131others(4): Show | 7 | HG01123.hp2 HG01515.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+24640G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989771 | ||||||
chr17:66989792
|
C | A | 3 | a0001c0001t0017g0059a0001c0001t0017g0172a0001c0001t0041g0155 | 3 | HG02451.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.220+24661C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989792 | ||||||
chr17:66989793
|
G | A | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+24662G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989793 | ||||||
chr17:66989815
|
G | A | 1 | a0001c0001t0011g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+24684G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989815 | ||||||
chr17:66989891
|
T | C | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+24760T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989891 | ||||||
chr17:66989958
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+24827C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989958 | ||||||
chr17:66990129
|
T | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 115 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.220+24998T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990129 | ||||||
chr17:66990199
|
G | T | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25068G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990199 | ||||||
chr17:66990313
|
C | T | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25182C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990313 | ||||||
chr17:66990425
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+25294C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990425 | ||||||
chr17:66990449
|
T | G | 18 | a0001c0001t0001g0094a0001c0001t0001g0133a0001c0001t0001g0134others(15): Show | 18 | HG00408.hp1 HG00621.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+25318T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990449 | ||||||
chr17:66990460
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0002g0340a0001c0002t0002g0342 | 3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+25329A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990460 | ||||||
chr17:66990546
|
C | T | 1 | a0001c0002t0002g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.220+25415C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990546 | ||||||
chr17:66990639
|
TAA | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+25509_220+2551 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990639 | ||||||
chr17:66990647
|
C | CTTATT | 20 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0095others(17): Show | 20 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.220+25553_220+2555 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | |||||
chr17:66990647
|
C | CTTATTTT others(3): Show |
36 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 37 | HG00621.hp1 HG00733.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.220+25548_220+2555 others(14): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | |||||
chr17:66990647
|
C | CTTATTTT others(8): Show |
9 | a0001c0001t0001g0083a0001c0001t0002g0035a0001c0001t0002g0160others(6): Show | 9 | HG01069.hp1 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+25543_220+2555 others(19): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | |||||
chr17:66990647
|
CTTATT | C | 13 | a0001c0001t0001g0203a0001c0001t0001g0219a0001c0001t0002g0099others(10): Show | 14 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.220+25553_220+2555 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | |||||
chr17:66990647
|
CTTATTTT others(3): Show |
C | 1 | a0001c0001t0002g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.220+25548_220+2555 others(14): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | |||||
chr17:66990660
|
ATTTTATT others(14): Show |
A | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25533_220+2555 others(25): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990660 | |||||
chr17:66990665
|
ATTTTATT others(9): Show |
A | 10 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+25538_220+2555 others(20): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990665 | |||||
chr17:66990675
|
ATTTTAT | A | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+25548_220+2555 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990675 | |||||
chr17:66990681
|
T | TTTTA | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25562_220+2556 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990681 | |||||
chr17:66990685
|
A | ATTTTATT others(4): Show |
5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+25557_220+2555 others(15): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990685 | |||||
chr17:66990704
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0003g0200 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.220+25573G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990704 | ||||||
chr17:66990810
|
A | G | 14 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(11): Show | 15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+25679A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990810 | ||||||
chr17:66990839
|
C | A | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25708C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990839 | ||||||
chr17:66990870
|
C | T | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25739C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990870 | ||||||
chr17:66990896
|
G | C | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25765G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990896 | ||||||
chr17:66991076
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0003g0154 | 2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+25945T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991076 | ||||||
chr17:66991078
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0003g0154 | 2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+25947G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991078 | ||||||
chr17:66991337
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+26206C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991337 | ||||||
chr17:66991337
|
C | CA | 56 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(53): Show | 58 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.220+26215dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66991337 | |||||
chr17:66991344
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.220+26213A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991344 | ||||||
chr17:66991353
|
C | T | 8 | a0001c0001t0003g0005a0001c0001t0003g0233a0001c0001t0003g0235others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+26222C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991353 | ||||||
chr17:66991445
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+26314A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991445 | ||||||
chr17:66991465
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0011g0190others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+26334G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991465 | ||||||
chr17:66991553
|
G | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(56): Show | 61 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.220+26422G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991553 | ||||||
chr17:66991592
|
A | G | 16 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+26461A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991592 | ||||||
chr17:66991608
|
G | T | 1 | a0001c0001t0011g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+26477G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991608 | ||||||
chr17:66991716
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.221-26473A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991716 | ||||||
chr17:66991946
|
T | A | 14 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(11): Show | 15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.221-26243T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991946 | ||||||
chr17:66991946
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221-26243T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991946 | ||||||
chr17:66992086
|
C | T | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-26103C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992086 | ||||||
chr17:66992160
|
T | TG | 22 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(19): Show | 23 | HG00597.hp1 HG00741.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.221-26017dupG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | |||||
chr17:66992160
|
TG | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 194 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.221-26017delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | |||||
chr17:66992160
|
TGG | T | 18 | a0001c0001t0001g0143a0001c0001t0001g0187a0001c0001t0002g0142others(15): Show | 18 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.221-26018_221-2601 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | |||||
chr17:66992164
|
G | T | 1 | a0001c0001t0008g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221-26025G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992164 | ||||||
chr17:66992166
|
G | C | 14 | a0001c0001t0002g0099a0001c0001t0002g0185a0001c0001t0006g0239others(11): Show | 14 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-26023G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992166 | ||||||
chr17:66992166
|
G | T | 9 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0260others(6): Show | 9 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-26023G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992166 | ||||||
chr17:66992167
|
G | T | 12 | a0001c0001t0001g0219a0001c0001t0002g0166a0001c0001t0002g0167others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-26022G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992167 | ||||||
chr17:66992265
|
A | G | 268 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(265): Show | 273 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.221-25924A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992265 | ||||||
chr17:66992282
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0003g0223 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221-25907C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992282 | ||||||
chr17:66992302
|
G | A | 3 | a0001c0005t0002g0029a0001c0005t0002g0031a0001c0005t0005g0030 | 3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.221-25887G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992302 | ||||||
chr17:66992392
|
C | A | 1 | a0001c0001t0001g0006 | 2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.221-25797C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992392 | ||||||
chr17:66992590
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 221 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.221-25599T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992590 | ||||||
chr17:66992794
|
T | A | 8 | a0001c0001t0003g0005a0001c0001t0003g0233a0001c0001t0003g0235others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-25395T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992794 | ||||||
chr17:66992806
|
C | T | 16 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-25383C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992806 | ||||||
chr17:66992819
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0280a0001c0001t0004g0152others(2): Show | 5 | NA18944.hp2 NA18947.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-25370G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992819 | ||||||
chr17:66992894
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0003g0046 | 2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-25295G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992894 | ||||||
chr17:66992919
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 116 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.221-25270G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992919 | ||||||
chr17:66992944
|
T | C | 1 | a0001c0001t0004g0304 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.221-25245T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992944 | ||||||
chr17:66992960
|
C | A | 10 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-25229C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992960 | ||||||
chr17:66993019
|
T | C | 1 | a0001c0002t0002g0295 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.221-25170T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993019 | ||||||
chr17:66993089
|
T | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 116 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.221-25100T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993089 | ||||||
chr17:66993111
|
GC | G | 12 | a0001c0001t0001g0219a0001c0001t0002g0191a0001c0001t0002g0238others(9): Show | 12 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-25077delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993111 | ||||||
chr17:66993213
|
G | T | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-24976G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993213 | ||||||
chr17:66993256
|
G | A | 6 | a0001c0001t0002g0333a0001c0001t0003g0273a0001c0001t0005g0277others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-24933G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993256 | ||||||
chr17:66993436
|
A | G | 16 | a0001c0001t0001g0187a0001c0001t0002g0166a0001c0001t0002g0167others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-24753A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993436 | ||||||
chr17:66993534
|
C | G | 5 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0011g0190others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-24655C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993534 | ||||||
chr17:66993535
|
C | G | 1 | a0001c0001t0011g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.221-24654C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993535 | ||||||
chr17:66993560
|
G | A | 2 | a0001c0001t0001g0094a0001c0002t0022g0090 | 2 | HG02132.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.221-24629G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993560 | ||||||
chr17:66993567
|
AC | A | 3 | a0001c0001t0001g0283a0001c0001t0003g0296a0001c0001t0003g0297 | 3 | HG02056.hp1 HG02293.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.221-24619delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66993567 | |||||
chr17:66993583
|
G | C | 1 | a0001c0001t0002g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-24606G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993583 | ||||||
chr17:66993669
|
G | T | 2 | a0001c0001t0001g0092a0001c0003t0003g0091 | 2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.221-24520G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993669 | ||||||
chr17:66993706
|
A | G | 10 | a0001c0001t0006g0240a0001c0001t0006g0241a0001c0001t0006g0243others(7): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-24483A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993706 | ||||||
chr17:66993854
|
C | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0054a0001c0001t0002g0173others(3): Show | 7 | HG00639.hp2 HG00733.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-24335C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993854 | ||||||
chr17:66993967
|
T | A | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-24222T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993967 | ||||||
chr17:66994020
|
TA | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0063others(17): Show | 21 | HG01109.hp1 HG01433.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-24156delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994020 | |||||
chr17:66994020
|
TAA | T | 107 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(104): Show | 109 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.221-24157_221-2415 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994020 | |||||
chr17:66994031
|
A | C | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-24158A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994031 | ||||||
chr17:66994049
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-24140C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994049 | ||||||
chr17:66994059
|
G | A | 7 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(4): Show | 7 | HG00438.hp1 HG00597.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-24130G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994059 | ||||||
chr17:66994091
|
G | C | 1 | a0001c0001t0003g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.221-24098G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994091 | ||||||
chr17:66994103
|
A | G | 4 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-24086A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994103 | ||||||
chr17:66994327
|
C | A | 1 | a0001c0001t0003g0218 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221-23862C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994327 | ||||||
chr17:66994327
|
C | CA | 99 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0047others(96): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.221-23844dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994327 | |||||
chr17:66994327
|
C | CAA | 19 | a0001c0001t0001g0112a0001c0001t0001g0153a0001c0001t0001g0217others(16): Show | 19 | HG00438.hp2 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-23845_221-2384 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994327 | |||||
chr17:66994339
|
A | AC | 14 | a0001c0001t0002g0238a0001c0001t0003g0181a0001c0001t0003g0229others(11): Show | 14 | HG01361.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-23850_221-2384 others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994339 | ||||||
chr17:66994339
|
A | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 96 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.221-23850A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994339 | ||||||
chr17:66994795
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0011g0190others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-23394G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994795 | ||||||
chr17:66994808
|
G | C | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.221-23381G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994808 | ||||||
chr17:66994834
|
G | C | 1 | a0001c0001t0006g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.221-23355G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994834 | ||||||
chr17:66994874
|
G | C | 3 | a0001c0001t0001g0285a0001c0001t0004g0314a0001c0001t0004g0339 | 3 | NA19012.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.221-23315G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994874 | ||||||
chr17:66994945
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 207 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.221-23244T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994945 | ||||||
chr17:66994960
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.221-23229G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994960 | ||||||
chr17:66994962
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.221-23227G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994962 | ||||||
chr17:66995006
|
G | A | 1 | a0001c0002t0002g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.221-23183G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995006 | ||||||
chr17:66995038
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(51): Show | 56 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.221-23151G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995038 | ||||||
chr17:66995112
|
A | C | 1 | a0001c0001t0011g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-23077A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995112 | ||||||
chr17:66995143
|
G | A | 1 | a0001c0001t0011g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.221-23046G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995143 | ||||||
chr17:66995146
|
C | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 121 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.221-23043C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995146 | ||||||
chr17:66995421
|
T | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 122 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.221-22768T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995421 | ||||||
chr17:66995456
|
C | A | 12 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(9): Show | 13 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-22733C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995456 | ||||||
chr17:66995493
|
G | A | 8 | a0001c0001t0002g0238a0001c0001t0002g0260a0001c0001t0002g0261others(5): Show | 8 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-22696G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995493 | ||||||
chr17:66995586
|
T | C | 1 | a0001c0001t0010g0278 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.221-22603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995586 | ||||||
chr17:66995618
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(200): Show | 208 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.221-22571A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995618 | ||||||
chr17:66995669
|
G | A | 2 | a0001c0001t0003g0324a0001c0002t0002g0322 | 2 | HG01981.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.221-22520G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995669 | ||||||
chr17:66995850
|
G | GA | 57 | a0001c0001t0001g0187a0001c0001t0002g0144a0001c0001t0002g0166others(54): Show | 58 | HG00735.hp1 HG01099.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.221-22330dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66995850 | |||||
chr17:66995871
|
G | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 120 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-22318G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995871 | ||||||
chr17:66996087
|
G | C | 12 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(9): Show | 13 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-22102G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996087 | ||||||
chr17:66996172
|
C | T | 1 | a0001c0002t0002g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.221-22017C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996172 | ||||||
chr17:66996253
|
A | AT | 117 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 120 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-21927dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996253 | |||||
chr17:66996275
|
C | T | 10 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-21914C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996275 | ||||||
chr17:66996327
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-21862T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996327 | ||||||
chr17:66996379
|
C | CT | 14 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0092others(11): Show | 14 | HG00597.hp2 HG01433.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-21791dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | |||||
chr17:66996379
|
CT | C | 9 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0131others(6): Show | 9 | HG01123.hp2 HG01515.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-21791delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | |||||
chr17:66996379
|
CTTT | C | 20 | a0001c0001t0002g0160a0001c0001t0003g0233a0001c0001t0003g0235others(17): Show | 21 | HG01099.hp2 HG01167.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-21793_221-2179 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | |||||
chr17:66996379
|
CTTTT | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 99 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-21794_221-2179 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | |||||
chr17:66996398
|
T | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-21791T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996398 | ||||||
chr17:66996411
|
G | A | 76 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0047others(73): Show | 77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.221-21778G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996411 | ||||||
chr17:66996536
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02083.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.221-21653C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996536 | ||||||
chr17:66996587
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.221-21602G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996587 | ||||||
chr17:66996835
|
A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 122 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.221-21354A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996835 | ||||||
chr17:66996896
|
C | T | 1 | a0001c0001t0006g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-21293C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996896 | ||||||
chr17:66996943
|
A | G | 1 | a0001c0001t0006g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221-21246A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996943 | ||||||
chr17:66996953
|
C | T | 3 | a0001c0001t0001g0139a0001c0002t0002g0137a0001c0002t0002g0138 | 3 | HG00544.hp1 NA18945.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.221-21236C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996953 | ||||||
chr17:66997245
|
AG | A | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-20940delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66997245 | |||||
chr17:66997339
|
C | A | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-20850C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997339 | ||||||
chr17:66997390
|
T | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 125 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.221-20799T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997390 | ||||||
chr17:66997471
|
A | T | 2 | a0001c0001t0002g0221a0001c0001t0002g0225 | 2 | HG01346.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.221-20718A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997471 | ||||||
chr17:66997474
|
T | A | 9 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0013g0236others(6): Show | 10 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-20715T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997474 | ||||||
chr17:66997583
|
G | A | 1 | a0001c0001t0027g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.221-20606G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997583 | ||||||
chr17:66997646
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 114 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.221-20543A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997646 | ||||||
chr17:66997807
|
G | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00741.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-20382G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997807 | ||||||
chr17:66997817
|
AAAAC | A | 12 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(9): Show | 13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-20352_221-2034 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66997817 | |||||
chr17:66998023
|
G | A | 13 | a0001c0001t0002g0160a0001c0001t0003g0233a0001c0001t0005g0177others(10): Show | 14 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-20166G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998023 | ||||||
chr17:66998079
|
A | G | 2 | a0001c0001t0007g0255a0001c0001t0007g0257 | 2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.221-20110A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998079 | ||||||
chr17:66998248
|
A | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(69): Show | 73 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.221-19941A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998248 | ||||||
chr17:66998258
|
T | C | 11 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(8): Show | 11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-19931T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998258 | ||||||
chr17:66998316
|
G | A | 10 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(7): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-19873G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998316 | ||||||
chr17:66998482
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.221-19707C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998482 | ||||||
chr17:66998483
|
G | A | 13 | a0001c0001t0002g0160a0001c0001t0003g0233a0001c0001t0005g0177others(10): Show | 14 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-19706G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998483 | ||||||
chr17:66998607
|
G | A | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-19582G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998607 | ||||||
chr17:66999043
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.221-19146G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999043 | ||||||
chr17:66999092
|
G | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 72 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.221-19097G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999092 | ||||||
chr17:66999183
|
T | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0092others(10): Show | 13 | HG01433.hp1 HG01433.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-19006T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999183 | ||||||
chr17:66999273
|
A | AGTT | 12 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(9): Show | 13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-18914_221-1891 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999273 | |||||
chr17:66999275
|
T | TTGG | 155 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 159 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.221-18891_221-1888 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999275 | |||||
chr17:66999275
|
T | TTGGTGG | 21 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(18): Show | 21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-18894_221-1888 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999275 | |||||
chr17:66999278
|
G | T | 1 | a0001c0001t0038g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.221-18911G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999278 | ||||||
chr17:66999281
|
G | T | 1 | a0001c0001t0038g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.221-18908G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999281 | ||||||
chr17:66999339
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.221-18850A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999339 | ||||||
chr17:66999346
|
C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18843C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999346 | ||||||
chr17:66999368
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18821G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999368 | ||||||
chr17:66999454
|
G | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.221-18735G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999454 | ||||||
chr17:66999476
|
T | G | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-18713T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999476 | ||||||
chr17:66999519
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 124 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.221-18670A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999519 | ||||||
chr17:66999653
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18536G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999653 | ||||||
chr17:66999726
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18463C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999726 | ||||||
chr17:66999753
|
AC | A | 12 | a0001c0001t0001g0104a0001c0001t0001g0276a0001c0001t0001g0305others(9): Show | 12 | HG00738.hp1 HG01346.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-18435delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999753 | ||||||
chr17:66999784
|
G | A | 10 | a0001c0001t0002g0264a0001c0001t0003g0266a0001c0001t0003g0268others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-18405G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999784 | ||||||
chr17:66999805
|
A | G | 1 | a0001c0003t0003g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.221-18384A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999805 | ||||||
chr17:66999891
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-18298G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999891 | ||||||
chr17:66999933
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.221-18256G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999933 | ||||||
chr17:66999943
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-18246C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999943 | ||||||
chr17:67000040
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0003g0046 | 2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-18149G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000040 | ||||||
chr17:67000105
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18084A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000105 | ||||||
chr17:67000172
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.221-18017C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000172 | ||||||
chr17:67000414
|
GT | G | 7 | a0001c0001t0001g0214a0001c0001t0002g0173a0001c0001t0002g0260others(4): Show | 7 | HG02071.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-17763delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67000414 | |||||
chr17:67000415
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.221-17774T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000415 | ||||||
chr17:67000416
|
T | TG | 96 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(93): Show | 99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-17773_221-1777 others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000416 | ||||||
chr17:67000417
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.221-17772T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000417 | ||||||
chr17:67000544
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.221-17645G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000544 | ||||||
chr17:67000546
|
G | A | 1 | a0001c0001t0005g0182 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-17643G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000546 | ||||||
chr17:67000591
|
G | A | 1 | a0001c0001t0007g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-17598G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000591 | ||||||
chr17:67000592
|
A | C | 1 | a0001c0001t0007g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-17597A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000592 | ||||||
chr17:67000598
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-17591C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000598 | ||||||
chr17:67000599
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-17590G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000599 | ||||||
chr17:67000883
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0146 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.221-17306C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000883 | ||||||
chr17:67000903
|
A | G | 10 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(7): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-17286A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000903 | ||||||
chr17:67001105
|
C | T | 4 | a0001c0001t0002g0160a0001c0001t0011g0190a0001c0001t0011g0344others(1): Show | 4 | HG01358.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-17084C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001105 | ||||||
chr17:67001122
|
T | C | 21 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(18): Show | 21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-17067T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001122 | ||||||
chr17:67001161
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221-17028C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001161 | ||||||
chr17:67001289
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0095 | 2 | HG01358.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.221-16900A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001289 | ||||||
chr17:67001308
|
A | G | 73 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0047others(70): Show | 75 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.221-16881A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001308 | ||||||
chr17:67001373
|
C | G | 2 | a0001c0001t0003g0296a0001c0001t0003g0297 | 2 | HG02293.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.221-16816C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001373 | ||||||
chr17:67001420
|
G | A | 1 | a0001c0002t0002g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.221-16769G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001420 | ||||||
chr17:67001703
|
C | T | 1 | a0001c0002t0002g0342 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.221-16486C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001703 | ||||||
chr17:67001708
|
A | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 6 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-16481A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001708 | ||||||
chr17:67001757
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.221-16432G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001757 | ||||||
chr17:67001844
|
G | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 120 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-16345G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001844 | ||||||
chr17:67001959
|
G | A | 1 | a0001c0001t0005g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.221-16230G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001959 | ||||||
chr17:67001977
|
C | T | 21 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(18): Show | 21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-16212C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001977 | ||||||
chr17:67002030
|
G | GGTATGAA | 15 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(12): Show | 16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16159_221-1615 others(11): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002030 | ||||||
chr17:67002031
|
A | T | 15 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(12): Show | 16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16158A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002031 | ||||||
chr17:67002032
|
C | A | 15 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(12): Show | 16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16157C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002032 | ||||||
chr17:67002137
|
C | T | 2 | a0001c0001t0002g0198a0001c0001t0005g0197 | 2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.221-16052C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002137 | ||||||
chr17:67002143
|
T | C | 2 | a0001c0001t0002g0198a0001c0001t0005g0197 | 2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.221-16046T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002143 | ||||||
chr17:67002198
|
C | T | 1 | a0001c0005t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.221-15991C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002198 | ||||||
chr17:67002212
|
A | T | 1 | a0001c0001t0007g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-15977A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002212 | ||||||
chr17:67002264
|
C | G | 10 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(7): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-15925C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002264 | ||||||
chr17:67002384
|
C | T | 18 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(15): Show | 19 | HG01243.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-15805C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002384 | ||||||
chr17:67002393
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-15796A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002393 | ||||||
chr17:67002567
|
C | A | 1 | a0001c0001t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.221-15622C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002567 | ||||||
chr17:67002618
|
T | TTC | 19 | a0001c0001t0001g0045a0001c0001t0002g0166a0001c0001t0002g0167others(16): Show | 19 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-15544_221-1554 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTC | 63 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0075others(60): Show | 64 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.221-15546_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTC | 12 | a0001c0001t0001g0212a0001c0001t0001g0227a0001c0001t0001g0299others(9): Show | 13 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.221-15548_221-1554 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(7): Show |
3 | a0001c0002t0002g0114a0001c0003t0003g0106a0001c0003t0003g0107 | 3 | HG03710.hp2 HG04204.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.221-15556_221-1554 others(18): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(9): Show |
3 | a0001c0001t0007g0252a0001c0002t0007g0256a0001c0003t0002g0001 | 4 | HG01256.hp1 HG01258.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-15558_221-1554 others(20): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(11): Show |
3 | a0001c0001t0007g0254a0001c0001t0007g0255a0001c0003t0001g0071 | 3 | HG00438.hp1 HG03704.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.221-15560_221-1554 others(22): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(13): Show |
2 | a0001c0001t0007g0253a0001c0003t0003g0091 | 2 | HG02602.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.221-15562_221-1554 others(24): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(15): Show |
3 | a0001c0001t0009g0237a0001c0002t0002g0121a0001c0003t0018g0259 | 3 | HG02027.hp1 HG03654.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.221-15564_221-1554 others(26): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
T | TTCTCTCT others(17): Show |
1 | a0001c0001t0007g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.221-15566_221-1554 others(28): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
TTC | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0187a0001c0001t0001g0215others(19): Show | 23 | HG00621.hp1 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.221-15544_221-1554 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002618
|
TTCTC | T | 5 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0001t0008g0262others(2): Show | 5 | HG01099.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-15546_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | |||||
chr17:67002638
|
C | CTCTG | 4 | a0001c0001t0008g0002a0001c0001t0008g0123a0001c0001t0010g0111others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-15548_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002638 | |||||
chr17:67002869
|
C | A | 10 | a0001c0001t0002g0160a0001c0001t0002g0238a0001c0001t0002g0260others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-15320C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002869 | ||||||
chr17:67002887
|
T | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(96): Show | 102 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.221-15302T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002887 | ||||||
chr17:67003002
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-15187G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003002 | ||||||
chr17:67003011
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-15178G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003011 | ||||||
chr17:67003085
|
G | A | 3 | a0001c0001t0002g0289a0001c0001t0003g0288a0001c0001t0004g0286 | 3 | HG02602.hp1 HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.221-15104G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003085 | ||||||
chr17:67003149
|
C | A | 11 | a0001c0001t0003g0233a0001c0001t0005g0177a0001c0001t0006g0240others(8): Show | 12 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-15040C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003149 | ||||||
chr17:67003410
|
G | C | 1 | a0001c0001t0004g0125 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.221-14779G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003410 | ||||||
chr17:67003582
|
A | AT | 5 | a0001c0001t0002g0035a0001c0001t0003g0034a0001c0001t0003g0273others(2): Show | 5 | HG02109.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-14604dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67003582 | |||||
chr17:67003745
|
T | C | 5 | a0001c0003t0001g0071a0001c0003t0002g0001a0001c0003t0003g0091others(2): Show | 6 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-14444T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003745 | ||||||
chr17:67003754
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.221-14435C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003754 | ||||||
chr17:67004058
|
G | A | 2 | a0001c0001t0004g0304a0001c0001t0016g0307 | 2 | HG02683.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.221-14131G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004058 | ||||||
chr17:67004103
|
C | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 117 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-14086C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004103 | ||||||
chr17:67004277
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 117 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-13912G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004277 | ||||||
chr17:67004280
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221-13909G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004280 | ||||||
chr17:67004347
|
C | T | 1 | a0001c0003t0003g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.221-13842C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004347 | ||||||
chr17:67004358
|
A | G | 8 | a0001c0001t0006g0239a0001c0001t0012g0019a0001c0001t0012g0061others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-13831A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004358 | ||||||
chr17:67004490
|
G | A | 1 | a0001c0001t0008g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221-13699G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004490 | ||||||
chr17:67004550
|
C | T | 8 | a0001c0001t0006g0239a0001c0001t0012g0019a0001c0001t0012g0061others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-13639C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004550 | ||||||
chr17:67004699
|
C | T | 5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-13490C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004699 | ||||||
chr17:67004773
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.221-13416G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004773 | ||||||
chr17:67004812
|
T | C | 21 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(18): Show | 21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-13377T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004812 | ||||||
chr17:67005151
|
A | G | 9 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-13038A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005151 | ||||||
chr17:67005169
|
A | G | 71 | a0001c0001t0001g0187a0001c0001t0002g0160a0001c0001t0002g0166others(68): Show | 74 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-13020A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005169 | ||||||
chr17:67005466
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.221-12723C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005466 | ||||||
chr17:67005543
|
C | G | 1 | a0001c0001t0030g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.221-12646C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005543 | ||||||
chr17:67005685
|
G | A | 6 | a0001c0001t0003g0005a0001c0001t0003g0235a0001c0001t0005g0182others(3): Show | 7 | HG01243.hp2 HG01891.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-12504G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005685 | ||||||
chr17:67005795
|
G | A | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.221-12394G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005795 | ||||||
chr17:67005887
|
C | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0094a0001c0002t0022g0090 | 3 | HG02132.hp2 NA18994.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.221-12302C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005887 | ||||||
chr17:67005917
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-12272A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005917 | ||||||
chr17:67005991
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.221-12198T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005991 | ||||||
chr17:67006104
|
G | C | 1 | a0001c0001t0003g0018 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-12085G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006104 | ||||||
chr17:67006133
|
A | G | 11 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(8): Show | 11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-12056A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006133 | ||||||
chr17:67006250
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0002g0298 | 2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.221-11939C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006250 | ||||||
chr17:67006312
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.221-11877C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006312 | ||||||
chr17:67006316
|
G | A | 11 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(8): Show | 11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-11873G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006316 | ||||||
chr17:67006533
|
C | T | 6 | a0001c0003t0001g0071a0001c0003t0002g0001a0001c0003t0003g0091others(3): Show | 7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-11656C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006533 | ||||||
chr17:67006690
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0011g0190 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-11499C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006690 | ||||||
chr17:67006843
|
G | T | 10 | a0001c0001t0005g0177a0001c0001t0006g0240a0001c0001t0006g0241others(7): Show | 11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-11346G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006843 | ||||||
chr17:67006844
|
C | T | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-11345C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006844 | ||||||
chr17:67007090
|
G | A | 2 | a0001c0001t0001g0315a0001c0001t0003g0331 | 2 | HG02015.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.221-11099G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007090 | ||||||
chr17:67007119
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | NA18970.hp1 NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.221-11070G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007119 | ||||||
chr17:67007179
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-11010C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007179 | ||||||
chr17:67007202
|
A | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0131a0001c0001t0002g0087others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-10987A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007202 | ||||||
chr17:67007284
|
G | T | 11 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(8): Show | 11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-10905G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007284 | ||||||
chr17:67007407
|
G | C | 9 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-10782G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007407 | ||||||
chr17:67007497
|
T | C | 1 | a0001c0002t0002g0136 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.221-10692T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007497 | ||||||
chr17:67007885
|
T | C | 1 | a0001c0001t0007g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.221-10304T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007885 | ||||||
chr17:67007967
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.221-10222T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007967 | ||||||
chr17:67008166
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 77 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-10023C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008166 | ||||||
chr17:67008194
|
C | G | 1 | a0001c0001t0001g0299 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.221-9995C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008194 | ||||||
chr17:67008271
|
C | T | 1 | a0001c0001t0003g0324 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.221-9918C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008271 | ||||||
chr17:67008285
|
T | C | 86 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(83): Show | 88 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.221-9904T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008285 | ||||||
chr17:67008399
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 74 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-9790G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008399 | ||||||
chr17:67008547
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0003g0046 | 2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-9642C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008547 | ||||||
chr17:67008590
|
C | T | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-9599C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008590 | ||||||
chr17:67008617
|
A | G | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-9572A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008617 | ||||||
chr17:67008821
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9368T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008821 | ||||||
chr17:67008822
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9367G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008822 | ||||||
chr17:67008823
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9366C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008823 | ||||||
chr17:67008890
|
A | C | 3 | a0001c0001t0008g0002a0001c0001t0008g0123a0001c0001t0039g0124 | 4 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-9299A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008890 | ||||||
chr17:67008904
|
G | A | 73 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 76 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.221-9285G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008904 | ||||||
chr17:67008904
|
G | C | 84 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(81): Show | 86 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.221-9285G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008904 | ||||||
chr17:67008912
|
T | G | 73 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 76 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.221-9277T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008912 | ||||||
chr17:67008941
|
CCT | C | 9 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-9247_221-9246d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008941 | ||||||
chr17:67009042
|
A | T | 1 | a0001c0001t0003g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.221-9147A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009042 | ||||||
chr17:67009058
|
A | T | 5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-9131A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009058 | ||||||
chr17:67009200
|
T | C | 5 | a0001c0003t0001g0071a0001c0003t0002g0001a0001c0003t0003g0091others(2): Show | 6 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-8989T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009200 | ||||||
chr17:67009365
|
CCT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 74 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-8821_221-8820d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009365 | |||||
chr17:67009388
|
G | T | 10 | a0001c0001t0005g0177a0001c0001t0006g0240a0001c0001t0006g0241others(7): Show | 11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-8801G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009388 | ||||||
chr17:67009500
|
A | AGCT | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8688_221-8687i others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009500 | |||||
chr17:67009503
|
G | GCC | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8686_221-8685i others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009503 | ||||||
chr17:67009505
|
A | T | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8684A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009505 | ||||||
chr17:67009508
|
T | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8681T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009508 | ||||||
chr17:67009509
|
C | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8680C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009509 | ||||||
chr17:67009580
|
G | A | 1 | a0001c0001t0005g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221-8609G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009580 | ||||||
chr17:67009643
|
T | G | 2 | a0001c0001t0002g0186a0001c0001t0034g0189 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.221-8546T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009643 | ||||||
chr17:67009719
|
T | C | 99 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(96): Show | 102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.221-8470T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009719 | ||||||
chr17:67009730
|
C | T | 6 | a0001c0003t0001g0071a0001c0003t0002g0001a0001c0003t0003g0091others(3): Show | 7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-8459C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009730 | ||||||
chr17:67009853
|
C | CA | 9 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-8335dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009853 | |||||
chr17:67009922
|
C | T | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(3): Show | 6 | HG01099.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-8267C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009922 | ||||||
chr17:67009923
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(59): Show | 64 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.221-8266G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009923 | ||||||
chr17:67010104
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221-8085G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010104 | ||||||
chr17:67010202
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.221-7987G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010202 | ||||||
chr17:67010339
|
A | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0196 | 3 | HG02083.hp1 HG02155.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.221-7850A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010339 | ||||||
chr17:67010452
|
T | C | 9 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-7737T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010452 | ||||||
chr17:67010549
|
A | C | 4 | a0001c0001t0001g0328a0001c0001t0003g0077a0001c0002t0002g0076others(1): Show | 4 | HG01361.hp1 HG01952.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-7640A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010549 | ||||||
chr17:67010623
|
CT | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0004g0314others(1): Show | 4 | HG00597.hp1 NA19067.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-7563delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67010623 | |||||
chr17:67010852
|
G | T | 80 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(77): Show | 82 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.221-7337G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010852 | ||||||
chr17:67010939
|
C | T | 1 | a0001c0001t0007g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.221-7250C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010939 | ||||||
chr17:67010972
|
G | A | 10 | a0001c0001t0005g0177a0001c0001t0006g0240a0001c0001t0006g0241others(7): Show | 11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-7217G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010972 | ||||||
chr17:67010985
|
C | G | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-7204C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010985 | ||||||
chr17:67011311
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0015g0302a0001c0001t0015g0308 | 3 | HG00741.hp1 HG01168.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.221-6878T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011311 | ||||||
chr17:67011468
|
A | C | 1 | a0001c0001t0002g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-6721A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011468 | ||||||
chr17:67011509
|
C | T | 14 | a0001c0001t0002g0160a0001c0001t0002g0166a0001c0001t0002g0167others(11): Show | 14 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-6680C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011509 | ||||||
chr17:67011624
|
G | GGAAT | 9 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0002g0086others(6): Show | 9 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-6538_221-6535d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011624 | |||||
chr17:67011624
|
GGAAT | G | 4 | a0001c0001t0003g0296a0001c0001t0003g0297a0002c0004t0001g0272others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6538_221-6535d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011624 | |||||
chr17:67011651
|
ATGAG | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 86 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.221-6533_221-6530d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011651 | |||||
chr17:67011655
|
G | A | 17 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0178others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-6534G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011655 | ||||||
chr17:67011687
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6502G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011687 | ||||||
chr17:67011818
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221-6371T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011818 | ||||||
chr17:67011856
|
T | C | 4 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6333T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011856 | ||||||
chr17:67012107
|
T | C | 6 | a0001c0001t0013g0258a0001c0001t0016g0100a0001c0002t0002g0023others(3): Show | 6 | HG01496.hp2 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-6082T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012107 | ||||||
chr17:67012544
|
A | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.221-5645A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012544 | ||||||
chr17:67012932
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.221-5257C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012932 | ||||||
chr17:67013219
|
T | C | 8 | a0001c0001t0006g0239a0001c0001t0012g0019a0001c0001t0012g0061others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4970T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013219 | ||||||
chr17:67013245
|
G | A | 8 | a0001c0001t0006g0239a0001c0001t0012g0019a0001c0001t0012g0061others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4944G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013245 | ||||||
chr17:67013326
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.221-4863C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013326 | ||||||
chr17:67013433
|
A | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0096a0001c0001t0001g0149others(6): Show | 9 | HG00558.hp1 HG02083.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-4756A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013433 | ||||||
chr17:67013435
|
T | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(69): Show | 74 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.221-4754T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013435 | ||||||
chr17:67013669
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0034g0189 | 3 | HG02486.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.221-4520G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013669 | ||||||
chr17:67013769
|
C | T | 7 | a0001c0001t0002g0238a0001c0001t0002g0260a0001c0001t0002g0261others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-4420C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013769 | ||||||
chr17:67013803
|
C | CA | 133 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(130): Show | 137 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.221-4374dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67013803 | |||||
chr17:67013881
|
C | T | 14 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(11): Show | 15 | HG00735.hp1 HG01256.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-4308C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013881 | ||||||
chr17:67013883
|
A | G | 13 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0177others(10): Show | 14 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-4306A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013883 | ||||||
chr17:67013964
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.221-4225T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013964 | ||||||
chr17:67013976
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0006g0243 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.221-4213G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013976 | ||||||
chr17:67013999
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.221-4190G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013999 | ||||||
chr17:67014281
|
C | A | 3 | a0001c0001t0002g0333a0001c0001t0005g0277a0001c0001t0005g0332 | 3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.221-3908C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014281 | ||||||
chr17:67014327
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(119): Show | 127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.221-3862G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014327 | ||||||
chr17:67014328
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-3861C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014328 | ||||||
chr17:67014571
|
T | C | 28 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.221-3618T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014571 | ||||||
chr17:67014631
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.221-3558T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014631 | ||||||
chr17:67014643
|
T | TA | 28 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.221-3539dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014643 | |||||
chr17:67014701
|
C | T | 1 | a0001c0001t0011g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.221-3488C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014701 | ||||||
chr17:67014915
|
C | T | 9 | a0001c0001t0002g0160a0001c0001t0005g0178a0001c0001t0005g0179others(6): Show | 9 | HG02258.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-3274C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014915 | ||||||
chr17:67014943
|
C | CA | 41 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(38): Show | 43 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.221-3230dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014943 | |||||
chr17:67014943
|
C | CAA | 26 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(23): Show | 28 | HG00408.hp2 HG01243.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.221-3231_221-3230d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014943 | |||||
chr17:67014956
|
A | AAG | 6 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0270others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-3232_221-3231i others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014956 | |||||
chr17:67014956
|
A | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-3233A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014956 | ||||||
chr17:67015092
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-3097C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015092 | ||||||
chr17:67015358
|
C | G | 3 | a0001c0001t0002g0160a0001c0001t0011g0190a0001c0001t0011g0344 | 3 | HG02717.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-2831C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015358 | ||||||
chr17:67015378
|
G | A | 5 | a0001c0001t0002g0191a0001c0001t0003g0233a0001c0001t0008g0294others(2): Show | 5 | HG02723.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-2811G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015378 | ||||||
chr17:67015382
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0011g0190a0001c0001t0011g0344 | 3 | HG02717.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-2807A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015382 | ||||||
chr17:67015628
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.221-2561C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015628 | ||||||
chr17:67015658
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(56): Show | 60 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.221-2531A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015658 | ||||||
chr17:67015717
|
G | C | 3 | a0001c0005t0002g0029a0001c0005t0002g0031a0001c0005t0005g0030 | 3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.221-2472G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015717 | ||||||
chr17:67015992
|
C | T | 1 | a0001c0001t0005g0269 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.221-2197C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015992 | ||||||
chr17:67016009
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.221-2180T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016009 | ||||||
chr17:67016065
|
C | T | 6 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0270others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-2124C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016065 | ||||||
chr17:67016066
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.221-2123A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016066 | ||||||
chr17:67016121
|
T | C | 96 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(93): Show | 99 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-2068T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016121 | ||||||
chr17:67016238
|
A | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.221-1951A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016238 | ||||||
chr17:67016328
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.221-1861C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016328 | ||||||
chr17:67016339
|
C | T | 14 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0270others(11): Show | 14 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-1850C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016339 | ||||||
chr17:67016384
|
G | A | 1 | a0001c0001t0011g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-1805G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016384 | ||||||
chr17:67016457
|
G | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 41 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.221-1732G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016457 | ||||||
chr17:67016587
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-1602T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016587 | ||||||
chr17:67016646
|
G | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(188): Show | 196 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.221-1543G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016646 | ||||||
chr17:67016654
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0029g0053 | 3 | NA19004.hp1 NA19080.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.221-1535T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016654 | ||||||
chr17:67016882
|
G | A | 11 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(8): Show | 11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-1307G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016882 | ||||||
chr17:67016936
|
G | T | 15 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0270others(12): Show | 15 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-1253G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016936 | ||||||
chr17:67017088
|
T | G | 9 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 9 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-1101T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017088 | ||||||
chr17:67017091
|
TTTTGAGA others(435): Show |
T | 1 | a0001c0001t0003g0046 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.221-1087_221-646de others(1): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017091 | |||||
chr17:67017139
|
T | C | 3 | a0001c0001t0002g0333a0001c0001t0005g0277a0001c0001t0005g0332 | 3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.221-1050T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017139 | ||||||
chr17:67017170
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.221-1019A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017170 | ||||||
chr17:67017296
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-893C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017296 | ||||||
chr17:67017329
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.221-860A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017329 | ||||||
chr17:67017498
|
C | A | 6 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0002g0116others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-691C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017498 | ||||||
chr17:67017498
|
C | CGTT | 95 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(92): Show | 99 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-666_221-664dup others(3): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017498 | |||||
chr17:67017498
|
C | CGTTGTT | 4 | a0001c0001t0001g0065a0001c0003t0001g0113a0001c0003t0003g0159others(1): Show | 4 | HG00408.hp2 HG02015.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-669_221-664dup others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017498 | |||||
chr17:67017527
|
GTTGTTGT | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.221-658_221-652del others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017527 | |||||
chr17:67017549
|
T | C | 21 | a0001c0001t0002g0160a0001c0001t0005g0178a0001c0001t0005g0179others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-640T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017549 | ||||||
chr17:67017565
|
TG | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-622delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017565 | |||||
chr17:67017566
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-623G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017566 | ||||||
chr17:67017567
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-622G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017567 | ||||||
chr17:67017578
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-611C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017578 | ||||||
chr17:67017580
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-609C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017580 | ||||||
chr17:67017586
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0003g0005others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017586 | ||||||
chr17:67017611
|
G | A | 81 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(78): Show | 83 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.221-578G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017611 | ||||||
chr17:67017728
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221-461G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017728 | ||||||
chr17:67017768
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0094 | 2 | HG02132.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.221-421G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017768 | ||||||
chr17:67017782
|
C | T | 1 | a0001c0002t0002g0114 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.221-407C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017782 | ||||||
chr17:67017869
|
G | A | 148 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(145): Show | 153 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.221-320G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017869 | ||||||
chr17:67018085
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.221-104A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018085 | ||||||
chr17:67018089
|
C | A | 1 | a0001c0001t0033g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.221-100C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018089 | ||||||
chr17:67018107
|
C | G | 1 | a0001c0001t0010g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.221-82C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018107 | ||||||
chr17:67018138
|
G | T | 3 | a0001c0001t0001g0187a0001c0001t0002g0186a0001c0001t0034g0189 | 3 | HG02486.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.221-51G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018138 | ||||||
chr17:67018333
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0235 | 3 | HG03516.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304+61G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018333 | ||||||
chr17:67018399
|
T | C | 12 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(9): Show | 13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.304+127T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018399 | ||||||
chr17:67018476
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.304+204G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018476 | ||||||
chr17:67018725
|
A | C | 5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0263others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+453A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018725 | ||||||
chr17:67018817
|
T | C | 3 | a0001c0005t0002g0029a0001c0005t0002g0031a0001c0005t0005g0030 | 3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.304+545T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018817 | ||||||
chr17:67018821
|
G | T | 12 | a0001c0001t0003g0266a0001c0001t0003g0268a0001c0001t0005g0177others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.304+549G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018821 | ||||||
chr17:67018853
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.304+581A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018853 | ||||||
chr17:67018853
|
A | T | 1 | a0001c0001t0032g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.304+581A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018853 | ||||||
chr17:67018857
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.304+585G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018857 | ||||||
chr17:67018890
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0063 | 3 | HG01981.hp2 NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.304+618A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018890 | ||||||
chr17:67019199
|
G | A | 3 | a0001c0001t0002g0333a0001c0001t0005g0277a0001c0001t0005g0332 | 3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.304+927G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019199 | ||||||
chr17:67019234
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0007g0254 | 2 | NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.304+962A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019234 | ||||||
chr17:67019272
|
C | G | 5 | a0001c0001t0001g0092a0001c0001t0002g0088a0001c0001t0002g0144others(2): Show | 5 | HG03490.hp1 HG03492.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1000C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019272 | ||||||
chr17:67019465
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(40): Show | 44 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.304+1193C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019465 | ||||||
chr17:67019878
|
C | G | 1 | a0001c0003t0003g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.304+1606C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019878 | ||||||
chr17:67020017
|
G | A | 6 | a0001c0003t0001g0071a0001c0003t0002g0001a0001c0003t0003g0091others(3): Show | 7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1745G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020017 | ||||||
chr17:67020123
|
G | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0312others(4): Show | 7 | HG00408.hp2 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1851G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020123 | ||||||
chr17:67020143
|
C | CAATGCCA others(6): Show |
1 | a0001c0001t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.304+1872_304+1884d others(15): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67020143 | |||||
chr17:67020153
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304+1881C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020153 | ||||||
chr17:67020160
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304+1888C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020160 | ||||||
chr17:67020192
|
C | A | 9 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 9 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+1920C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020192 | ||||||
chr17:67020429
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.304+2157C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020429 | ||||||
chr17:67020498
|
C | T | 9 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0270others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+2226C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020498 | ||||||
chr17:67020564
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.304+2292C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020564 | ||||||
chr17:67020567
|
A | G | 95 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(92): Show | 98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.304+2295A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020567 | ||||||
chr17:67020729
|
A | G | 11 | a0001c0001t0002g0089a0001c0001t0002g0099a0001c0001t0002g0220others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.304+2457A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020729 | ||||||
chr17:67021052
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0009g0250a0001c0001t0009g0251others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2780T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021052 | ||||||
chr17:67021124
|
C | T | 1 | a0001c0001t0012g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.304+2852C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021124 | ||||||
chr17:67021156
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0034g0189 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.304+2884G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021156 | ||||||
chr17:67021160
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.304+2888C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021160 | ||||||
chr17:67021191
|
A | T | 1 | a0001c0003t0003g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.304+2919A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021191 | ||||||
chr17:67021200
|
T | TA | 9 | a0001c0001t0003g0024a0001c0001t0003g0319a0001c0001t0003g0320others(6): Show | 9 | HG00558.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.304+2943dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67021200 | |||||
chr17:67021200
|
TA | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0092others(26): Show | 29 | HG01069.hp1 HG01070.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.304+2943delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67021200 | |||||
chr17:67021290
|
G | GC | 343 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(340): Show | 351 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.304+3020dupC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67021290 | |||||
chr17:67021301
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0235a0001c0001t0005g0182others(2): Show | 6 | HG01243.hp2 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+3029G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021301 | ||||||
chr17:67021339
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304+3067T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021339 | ||||||
chr17:67021367
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0002g0054others(7): Show | 10 | HG01433.hp1 HG01433.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.304+3095T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021367 | ||||||
chr17:67021385
|
G | A | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.304+3113G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021385 | ||||||
chr17:67021391
|
G | A | 9 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+3119G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021391 | ||||||
chr17:67021468
|
C | G | 3 | a0002c0004t0001g0272a0002c0004t0002g0234a0002c0004t0003g0271 | 3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.304+3196C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021468 | ||||||
chr17:67021500
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.304+3228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021500 | ||||||
chr17:67021517
|
T | C | 12 | a0001c0001t0002g0264a0001c0001t0003g0266a0001c0001t0003g0268others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.304+3245T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021517 | ||||||
chr17:67021811
|
C | G | 19 | a0001c0001t0002g0186a0001c0001t0002g0261a0001c0001t0002g0263others(16): Show | 20 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.305-3049C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021811 | ||||||
chr17:67021916
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305-2944G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021916 | ||||||
chr17:67021933
|
G | A | 2 | a0001c0001t0003g0331a0001c0001t0004g0101 | 2 | NA18959.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.305-2927G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021933 | ||||||
chr17:67021957
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.305-2903A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021957 | ||||||
chr17:67022076
|
C | CT | 41 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0002g0099others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-2767dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67022076 | |||||
chr17:67022076
|
C | CTT | 81 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0037others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.305-2768_305-2767d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67022076 | |||||
chr17:67022099
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.305-2761G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022099 | ||||||
chr17:67022137
|
G | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(18): Show | 21 | HG00544.hp2 HG01891.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-2723G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022137 | ||||||
chr17:67022168
|
G | A | 8 | a0001c0001t0002g0238a0001c0001t0005g0074a0001c0001t0005g0228others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2692G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022168 | ||||||
chr17:67022279
|
T | C | 6 | a0001c0001t0005g0179a0001c0001t0011g0344a0001c0001t0035g0188others(3): Show | 6 | HG02717.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-2581T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022279 | ||||||
chr17:67022327
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.305-2533G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022327 | ||||||
chr17:67022598
|
A | T | 3 | a0002c0004t0001g0272a0002c0004t0002g0234a0002c0004t0003g0271 | 3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.305-2262A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022598 | ||||||
chr17:67022652
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0220 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.305-2208C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022652 | ||||||
chr17:67022691
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0235 | 3 | HG03516.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.305-2169C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022691 | ||||||
chr17:67022747
|
C | T | 1 | a0001c0001t0034g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.305-2113C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022747 | ||||||
chr17:67022810
|
T | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(144): Show | 151 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.305-2050T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022810 | ||||||
chr17:67022825
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0033others(82): Show | 88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.305-2035C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022825 | ||||||
chr17:67023007
|
G | A | 2 | a0001c0003t0003g0091a0001c0003t0018g0259 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-1853G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023007 | ||||||
chr17:67023099
|
C | T | 8 | a0001c0001t0002g0238a0001c0001t0005g0074a0001c0001t0005g0228others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-1761C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023099 | ||||||
chr17:67023143
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0003g0066a0001c0001t0003g0326others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-1717C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023143 | ||||||
chr17:67023188
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.305-1672C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023188 | ||||||
chr17:67023207
|
C | T | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.305-1653C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023207 | ||||||
chr17:67023270
|
C | CT | 189 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 193 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.305-1567dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | |||||
chr17:67023270
|
C | CTT | 15 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0140others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.305-1568_305-1567d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | |||||
chr17:67023270
|
CT | C | 20 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0195others(17): Show | 21 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.305-1567delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | |||||
chr17:67023339
|
G | A | 270 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(267): Show | 276 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.305-1521G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023339 | ||||||
chr17:67023359
|
T | C | 4 | a0001c0001t0001g0328a0001c0001t0003g0077a0001c0002t0002g0076others(1): Show | 4 | HG01361.hp1 HG01952.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-1501T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023359 | ||||||
chr17:67023377
|
G | C | 8 | a0001c0001t0002g0238a0001c0001t0005g0074a0001c0001t0005g0228others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-1483G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023377 | ||||||
chr17:67023433
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0021others(30): Show | 34 | HG00597.hp1 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.305-1427G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023433 | ||||||
chr17:67023574
|
CCTT | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(18): Show | 21 | HG00544.hp2 HG01891.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-1285_305-1283d others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023574 | ||||||
chr17:67023575
|
C | CT | 203 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0033others(200): Show | 207 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.305-1272dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023575 | |||||
chr17:67023629
|
T | C | 11 | a0001c0001t0002g0264a0001c0001t0003g0266a0001c0001t0003g0268others(8): Show | 12 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-1231T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023629 | ||||||
chr17:67023832
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.305-1028C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023832 | ||||||
chr17:67023834
|
C | T | 10 | a0001c0001t0001g0208a0001c0001t0002g0191a0001c0001t0003g0233others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.305-1026C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023834 | ||||||
chr17:67023845
|
G | A | 2 | a0001c0001t0003g0233a0001c0001t0008g0301 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.305-1015G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023845 | ||||||
chr17:67023940
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.305-920G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023940 | ||||||
chr17:67024040
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.305-820A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024040 | ||||||
chr17:67024082
|
T | C | 1 | a0001c0001t0008g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.305-778T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024082 | ||||||
chr17:67024096
|
T | G | 101 | a0001c0001t0001g0028a0001c0001t0001g0056a0001c0001t0001g0094others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.305-764T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024096 | ||||||
chr17:67024263
|
T | C | 2 | a0001c0001t0003g0273a0001c0001t0030g0183 | 2 | HG01361.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.305-597T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024263 | ||||||
chr17:67024399
|
C | T | 2 | a0001c0003t0003g0091a0001c0003t0018g0259 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-461C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024399 | ||||||
chr17:67024412
|
C | G | 8 | a0001c0001t0002g0238a0001c0001t0005g0074a0001c0001t0005g0228others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-448C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024412 | ||||||
chr17:67024430
|
C | G | 1 | a0001c0001t0001g0231 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.305-430C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024430 | ||||||
chr17:67024547
|
G | A | 2 | a0001c0003t0003g0091a0001c0003t0018g0259 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-313G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024547 | ||||||
chr17:67024561
|
C | G | 9 | a0001c0001t0001g0102a0001c0001t0002g0007a0001c0001t0002g0306others(6): Show | 10 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.305-299C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024561 | ||||||
chr17:67024615
|
A | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0033others(82): Show | 88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.305-245A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024615 | ||||||
chr17:67024657
|
C | T | 1 | a0001c0001t0005g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-203C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024657 | ||||||
chr17:67024711
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0140a0001c0001t0002g0054others(7): Show | 10 | HG01433.hp1 HG01433.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-149C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024711 | ||||||
chr17:67024717
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.305-143C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024717 | ||||||
chr17:67024796
|
C | T | 8 | a0001c0001t0002g0238a0001c0001t0005g0074a0001c0001t0005g0228others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-64C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024796 | ||||||
chr17:67024804
|
G | A | 1 | a0001c0001t0034g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.305-56G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024804 | ||||||
chr17:67024806
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-54G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024806 | ||||||
chr17:67024845
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.305-15C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024845 | ||||||
chr17:67025143
|
T | G | 1 | a0001c0002t0022g0090 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.445+143T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025143 | ||||||
chr17:67025276
|
C | T | 1 | a0001c0002t0002g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.445+276C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025276 | ||||||
chr17:67025343
|
A | T | 5 | a0001c0001t0002g0084a0001c0001t0002g0086a0001c0001t0002g0160others(2): Show | 5 | HG00639.hp1 HG01109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+343A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025343 | ||||||
chr17:67025407
|
G | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0276a0001c0001t0001g0305others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+407G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025407 | ||||||
chr17:67025423
|
A | C | 5 | a0001c0001t0002g0085a0001c0001t0002g0099a0001c0001t0003g0268others(2): Show | 5 | HG02922.hp1 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+423A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025423 | ||||||
chr17:67025444
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.445+444G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025444 | ||||||
chr17:67025456
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.445+456C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025456 | ||||||
chr17:67025488
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+488C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025488 | ||||||
chr17:67025515
|
A | G | 3 | a0001c0001t0002g0035a0001c0001t0002g0192a0001c0001t0019g0247 | 3 | HG01891.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.445+515A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025515 | ||||||
chr17:67025566
|
GC | G | 4 | a0001c0001t0006g0239a0001c0001t0021g0244a0001c0001t0038g0169others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+567delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025566 | ||||||
chr17:67025568
|
G | A | 5 | a0001c0001t0002g0151a0001c0001t0003g0048a0001c0001t0003g0321others(2): Show | 5 | HG00140.hp2 HG01070.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+568G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025568 | ||||||
chr17:67025630
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.445+630G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025630 | ||||||
chr17:67025647
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0003g0068a0001c0001t0003g0069 | 3 | HG00735.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445+647C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025647 | ||||||
chr17:67025648
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445+648G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025648 | ||||||
chr17:67025711
|
A | C | 4 | a0001c0001t0002g0186a0001c0001t0003g0034a0001c0001t0011g0190others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+711A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025711 | ||||||
chr17:67025795
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0003g0194a0001c0001t0003g0291others(2): Show | 5 | HG02683.hp2 NA18960.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+795T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025795 | ||||||
chr17:67025882
|
T | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(300): Show | 307 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.445+882T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025882 | ||||||
chr17:67026043
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(251): Show | 258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.445+1043T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026043 | ||||||
chr17:67026054
|
G | A | 1 | a0001c0001t0034g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.445+1054G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026054 | ||||||
chr17:67026459
|
G | A | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146 | 3 | HG03490.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.445+1459G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026459 | ||||||
chr17:67026485
|
CTGTATTT others(47): Show |
C | 52 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(49): Show | 52 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.445+1498_445+1551d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67026485 | |||||
chr17:67026517
|
A | G | 2 | a0001c0001t0005g0179a0001c0001t0037g0232 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445+1517A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026517 | ||||||
chr17:67026654
|
C | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0002g0289others(38): Show | 41 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.445+1654C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026654 | ||||||
chr17:67026679
|
G | GTGTGTGT others(57): Show |
1 | a0001c0001t0001g0227 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.445+1701_445+1764d others(66): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67026679 | |||||
chr17:67026875
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.445+1875C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026875 | ||||||
chr17:67026928
|
G | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0337a0001c0002t0002g0137others(2): Show | 5 | HG00544.hp1 NA18945.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+1928G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026928 | ||||||
chr17:67026959
|
A | C | 9 | a0001c0001t0017g0059a0001c0001t0017g0172a0001c0001t0021g0244others(6): Show | 9 | HG01099.hp1 HG01361.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+1959A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026959 | ||||||
chr17:67026971
|
C | T | 3 | a0001c0001t0002g0263a0001c0001t0005g0179a0001c0001t0037g0232 | 3 | HG01243.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.445+1971C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026971 | ||||||
chr17:67027026
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0115 | 2 | HG02015.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.445+2026C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027026 | ||||||
chr17:67027079
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.445+2079G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027079 | ||||||
chr17:67027131
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+2131C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027131 | ||||||
chr17:67027221
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0024g0210 | 2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.445+2221G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027221 | ||||||
chr17:67027275
|
C | T | 5 | a0001c0001t0021g0244a0001c0001t0026g0205a0001c0001t0030g0183others(2): Show | 5 | HG01361.hp2 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+2275C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027275 | ||||||
chr17:67027301
|
A | G | 298 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(295): Show | 301 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.445+2301A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027301 | ||||||
chr17:67027360
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+2360C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027360 | ||||||
chr17:67027511
|
G | T | 2 | a0001c0001t0002g0289a0001c0001t0003g0288 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.445+2511G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027511 | ||||||
chr17:67027514
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.445+2514T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027514 | ||||||
chr17:67027661
|
A | C | 1 | a0001c0001t0024g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.445+2661A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027661 | ||||||
chr17:67027661
|
A | G | 27 | a0001c0001t0001g0139a0001c0001t0001g0337a0001c0001t0021g0244others(24): Show | 27 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.445+2661A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027661 | ||||||
chr17:67027785
|
G | A | 1 | a0001c0001t0024g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-2681G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027785 | ||||||
chr17:67027968
|
T | A | 1 | a0001c0001t0035g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.446-2498T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027968 | ||||||
chr17:67027998
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.446-2468C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027998 | ||||||
chr17:67027999
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446-2467G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027999 | ||||||
chr17:67028024
|
A | T | 1 | a0001c0001t0005g0269 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-2442A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028024 | ||||||
chr17:67028072
|
T | C | 24 | a0001c0001t0001g0139a0001c0001t0001g0337a0001c0002t0002g0020others(21): Show | 24 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.446-2394T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028072 | ||||||
chr17:67028225
|
C | T | 2 | a0001c0001t0021g0244a0001c0001t0038g0169 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-2241C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028225 | ||||||
chr17:67028276
|
G | A | 11 | a0001c0001t0002g0186a0001c0001t0005g0074a0001c0001t0005g0178others(8): Show | 11 | HG01346.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-2190G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028276 | ||||||
chr17:67028281
|
C | T | 4 | a0001c0001t0017g0059a0001c0001t0017g0172a0001c0001t0024g0210others(1): Show | 4 | HG01099.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-2185C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028281 | ||||||
chr17:67028329
|
G | A | 3 | a0001c0001t0003g0233a0001c0001t0003g0266a0002c0004t0003g0271 | 3 | HG02055.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.446-2137G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028329 | ||||||
chr17:67028349
|
C | T | 2 | a0001c0005t0002g0029a0001c0005t0002g0031 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.446-2117C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028349 | ||||||
chr17:67028358
|
T | C | 2 | a0001c0005t0002g0029a0001c0005t0002g0031 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.446-2108T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028358 | ||||||
chr17:67028446
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.446-2020A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028446 | ||||||
chr17:67028477
|
C | T | 1 | a0001c0001t0010g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.446-1989C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028477 | ||||||
chr17:67028519
|
C | G | 1 | a0001c0001t0003g0319 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.446-1947C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028519 | ||||||
chr17:67028547
|
C | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0133others(11): Show | 14 | HG00438.hp2 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-1919C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028547 | ||||||
chr17:67028552
|
C | CA | 14 | a0001c0001t0001g0028a0001c0001t0003g0005a0001c0001t0003g0034others(11): Show | 15 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.446-1908dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67028552 | |||||
chr17:67028559
|
G | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(266): Show | 272 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.446-1907G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028559 | ||||||
chr17:67028565
|
C | A | 8 | a0001c0001t0002g0084a0001c0001t0002g0086a0001c0001t0002g0160others(5): Show | 8 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-1901C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028565 | ||||||
chr17:67028607
|
G | A | 1 | a0001c0002t0002g0342 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.446-1859G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028607 | ||||||
chr17:67028613
|
C | A | 1 | a0001c0001t0033g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-1853C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028613 | ||||||
chr17:67028613
|
C | T | 1 | a0001c0001t0024g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-1853C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028613 | ||||||
chr17:67028668
|
C | A | 1 | a0001c0001t0002g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-1798C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028668 | ||||||
chr17:67028733
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446-1733A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028733 | ||||||
chr17:67028870
|
C | T | 1 | a0001c0001t0004g0152 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.446-1596C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028870 | ||||||
chr17:67029059
|
G | A | 2 | a0001c0001t0021g0244a0001c0001t0038g0169 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-1407G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029059 | ||||||
chr17:67029163
|
C | A | 1 | a0001c0001t0024g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-1303C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029163 | ||||||
chr17:67029272
|
C | T | 1 | a0001c0001t0026g0205 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.446-1194C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029272 | ||||||
chr17:67029280
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.446-1186G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029280 | ||||||
chr17:67029287
|
G | A | 1 | a0001c0001t0011g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.446-1179G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029287 | ||||||
chr17:67029395
|
G | A | 57 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 57 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.446-1071G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029395 | ||||||
chr17:67029444
|
A | C | 44 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(41): Show | 44 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.446-1022A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029444 | ||||||
chr17:67029475
|
CA | C | 271 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(268): Show | 274 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.446-982delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67029475 | |||||
chr17:67029502
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.446-964C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029502 | ||||||
chr17:67029558
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(189): Show | 195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.446-908C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029558 | ||||||
chr17:67029570
|
G | T | 1 | a0001c0001t0033g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-896G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029570 | ||||||
chr17:67029580
|
G | T | 1 | a0001c0001t0006g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.446-886G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029580 | ||||||
chr17:67029582
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.446-884C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029582 | ||||||
chr17:67029637
|
A | AAAAC | 194 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(191): Show | 197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.446-809_446-806dup others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67029637 | |||||
chr17:67029716
|
C | T | 1 | a0001c0001t0033g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-750C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029716 | ||||||
chr17:67029733
|
A | C | 1 | a0001c0001t0031g0303 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.446-733A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029733 | ||||||
chr17:67029828
|
C | T | 3 | a0001c0001t0011g0190a0001c0001t0011g0344a0001c0001t0040g0274 | 3 | HG02647.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.446-638C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029828 | ||||||
chr17:67029895
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(300): Show | 308 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.446-571G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029895 | ||||||
chr17:67029973
|
C | T | 1 | a0001c0001t0024g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-493C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029973 | ||||||
chr17:67029988
|
C | T | 2 | a0001c0001t0005g0178a0001c0001t0005g0270 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.446-478C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029988 | ||||||
chr17:67030152
|
GGT | G | 69 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(66): Show | 70 | HG00597.hp1 HG00609.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.446-294_446-293del others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67030152 | |||||
chr17:67030152
|
GGTGT | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(229): Show | 236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.446-296_446-293del others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67030152 | |||||
chr17:67030156
|
T | G | 1 | a0001c0001t0001g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.446-310T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030156 | ||||||
chr17:67030158
|
T | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(170): Show | 175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.446-308T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030158 | ||||||
chr17:67030160
|
T | G | 2 | a0001c0001t0001g0187a0002c0004t0001g0272 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.446-306T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030160 | ||||||
chr17:67030215
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.446-251C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030215 | ||||||
chr17:67030399
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(177): Show | 184 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.446-67A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030399 | ||||||
chr17:67030400
|
C | T | 4 | a0001c0001t0012g0019a0001c0001t0012g0061a0001c0001t0012g0062others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-66C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030400 | ||||||
chr17:67030439
|
G | A | 1 | a0001c0003t0018g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.446-27G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030439 |