geneid | 7443 |
---|---|
ensemblid | ENSG00000100749.9 |
hgncid | 12718 |
symbol | VRK1 |
name | VRK serine/threonine kinase 1 |
refseq_nuc | NM_003384.3 |
refseq_prot | NP_003375.1 |
ensembl_nuc | ENST00000216639.8 |
ensembl_prot | ENSP00000216639.3 |
mane_status | MANE Select |
chr | chr14 |
start | 96797382 |
end | 96881609 |
strand | + |
ver | v1.2 |
region | chr14:96797382-96881609 |
region5000 | chr14:96792382-96886609 |
regionname0 | VRK1_chr14_96797382_96881609 |
regionname5000 | VRK1_chr14_96792382_96886609 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1191 | 106 | 15 | 28 | 43 | 5 | 15 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
c0002 | 1/0 | 1191 | 101 | 54 | 12 | 18 | 2 | 14 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
c0003 | 0/1 | 1191 | 70 | 19 | 20 | 16 | 3 | 11 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
c0004 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 473 | 276 | 86 | 60 | 78 | 10 | 40 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
t0002 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
t0003 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1191 | 106 | 15 | 28 | 43 | 5 | 15 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0002 | 1/0 | 1191 | 101 | 54 | 12 | 18 | 2 | 14 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0003 | 0/1 | 1191 | 70 | 19 | 20 | 16 | 3 | 11 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0002c0004 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1663 | 105 | 14 | 28 | 43 | 5 | 15 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0001t0002 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0002t0001 | 1/0 | 1663 | 100 | 53 | 12 | 18 | 2 | 14 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0002t0003 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0001c0003t0001 | 0/1 | 1663 | 70 | 19 | 20 | 16 | 3 | 11 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
a0002c0004t0001 | 0/0 | 1663 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | copy fasta | chr14 | 96792382 | 96886609 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | GBR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | GBR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00438 | hp2 | a0002 | c0004 | t0001 | g0184 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0062 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0069 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0016 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0067 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0244 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0044 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0074 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0068 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0092 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0061 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0080 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0063 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0240 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ASW | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0027 | EUR | TSI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0059 | REF | REF | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0196 | REF | REF | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96876085
|
G | A | 1 | a0002 | 1 | HG00438.hp2 | stop_gained | HIGH | c.1124G>A | p.Trp375* | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/13 | 1195/1663 | 1124/1191 | 375/396 | chr14 | 96876085 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96833516
|
A | G | 1 | a0001c0003 | 70 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
synonymous_variant | LOW | c.45A>G | p.Ala15Ala | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/13 | 116/1663 | 45/1191 | 15/396 | chr14 | 96833516 | ||
chr14:96855352
|
C | T | 2 | a0001c0001a0002c0004 | 107 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
synonymous_variant | LOW | c.705C>T | p.Gly235Gly | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/13 | 776/1663 | 705/1191 | 235/396 | chr14 | 96855352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96881263
|
C | G | 1 | a0001c0002t0003 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 13/13 | 55 | chr14 | 96881263 | |||||
chr14:96881388
|
C | T | 1 | a0001c0001t0002 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 13/13 | 180 | chr14 | 96881388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96797538
|
C | T | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+91C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797538 | ||||||
chr14:96797592
|
T | C | 134 | a0001c0001t0001g0039a0001c0002t0001g0008a0001c0002t0001g0017others(131): Show | 153 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.-6+145T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797592 | ||||||
chr14:96797716
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+269C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797716 | ||||||
chr14:96797737
|
C | T | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+290C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797737 | ||||||
chr14:96797775
|
G | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+328G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797775 | ||||||
chr14:96797813
|
G | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+366G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797813 | ||||||
chr14:96797937
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0138 | 4 | HG01891.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+490G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797937 | ||||||
chr14:96798045
|
A | G | 20 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(17): Show | 23 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.-6+598A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798045 | ||||||
chr14:96798241
|
C | T | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+794C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798241 | ||||||
chr14:96798247
|
C | G | 31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+800C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798247 | ||||||
chr14:96798495
|
A | G | 11 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0126others(8): Show | 13 | NA18943.hp2 NA18960.hp2 NA18962.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6+1048A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798495 | ||||||
chr14:96798530
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+1083G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798530 | ||||||
chr14:96798594
|
G | A | 2 | a0001c0003t0001g0037a0001c0003t0001g0038 | 2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-6+1147G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798594 | ||||||
chr14:96798835
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+1388C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798835 | ||||||
chr14:96798884
|
C | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1437C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798884 | ||||||
chr14:96798958
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-6+1511T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798958 | ||||||
chr14:96798970
|
G | A | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1523G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798970 | ||||||
chr14:96799026
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-6+1579A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799026 | ||||||
chr14:96799326
|
C | CT | 26 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(23): Show | 29 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-6+1889dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799326 | |||||
chr14:96799576
|
A | G | 2 | a0001c0002t0001g0245a0001c0002t0001g0246 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-6+2129A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799576 | ||||||
chr14:96799792
|
G | T | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+2345G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799792 | ||||||
chr14:96799947
|
C | CT | 5 | a0001c0001t0001g0234a0001c0003t0001g0092a0001c0003t0001g0093others(2): Show | 5 | HG02738.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2517dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799947 | |||||
chr14:96799947
|
CT | C | 13 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 14 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6+2517delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799947 | |||||
chr14:96800015
|
C | A | 126 | a0001c0002t0001g0008a0001c0002t0001g0018a0001c0002t0001g0019others(123): Show | 144 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-6+2568C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800015 | ||||||
chr14:96800174
|
A | G | 1 | a0001c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-6+2727A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800174 | ||||||
chr14:96800720
|
A | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+3273A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800720 | ||||||
chr14:96800790
|
G | A | 6 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+3343G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800790 | ||||||
chr14:96800813
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+3366T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800813 | ||||||
chr14:96800844
|
G | T | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6+3397G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800844 | ||||||
chr14:96801252
|
A | T | 2 | a0001c0003t0001g0016a0001c0003t0001g0082 | 3 | HG01069.hp2 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-6+3805A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801252 | ||||||
chr14:96801358
|
G | A | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6+3911G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801358 | ||||||
chr14:96801850
|
G | A | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+4403G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801850 | ||||||
chr14:96801923
|
A | G | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+4476A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801923 | ||||||
chr14:96802209
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | NA18966.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-6+4762C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802209 | ||||||
chr14:96802210
|
G | A | 59 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(56): Show | 65 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-6+4763G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802210 | ||||||
chr14:96802221
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+4774C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802221 | ||||||
chr14:96802287
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-6+4840C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802287 | ||||||
chr14:96802318
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+4871A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802318 | ||||||
chr14:96802321
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-6+4874C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802321 | ||||||
chr14:96802394
|
A | G | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+4947A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802394 | ||||||
chr14:96802403
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-6+4956C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802403 | ||||||
chr14:96802565
|
C | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5118C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802565 | ||||||
chr14:96802635
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+5188G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802635 | ||||||
chr14:96802796
|
T | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+5349T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802796 | ||||||
chr14:96802860
|
C | A | 65 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(62): Show | 77 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-6+5413C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802860 | ||||||
chr14:96802965
|
A | G | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-6+5518A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802965 | ||||||
chr14:96803030
|
C | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+5583C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803030 | ||||||
chr14:96803168
|
A | AT | 9 | a0001c0001t0001g0005a0001c0001t0001g0192a0001c0001t0001g0227others(6): Show | 11 | HG01952.hp1 HG02258.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+5741dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96803168 | |||||
chr14:96803168
|
AT | A | 32 | a0001c0001t0001g0143a0001c0001t0001g0193a0001c0002t0001g0018others(29): Show | 36 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6+5741delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96803168 | |||||
chr14:96803186
|
T | C | 59 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(56): Show | 71 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.-6+5739T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803186 | ||||||
chr14:96803187
|
T | A | 2 | a0001c0003t0001g0009a0001c0003t0001g0041 | 3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+5740T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803187 | ||||||
chr14:96803228
|
A | G | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+5781A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803228 | ||||||
chr14:96803257
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-6+5810C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803257 | ||||||
chr14:96803305
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5858G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803305 | ||||||
chr14:96803315
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-6+5868C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803315 | ||||||
chr14:96803388
|
C | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5941C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803388 | ||||||
chr14:96803740
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+6293A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803740 | ||||||
chr14:96804502
|
A | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 267 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.-6+7055A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804502 | ||||||
chr14:96804555
|
T | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+7108T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804555 | ||||||
chr14:96804660
|
A | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0226 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-6+7213A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804660 | ||||||
chr14:96804892
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+7445A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804892 | ||||||
chr14:96804919
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+7472T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804919 | ||||||
chr14:96804954
|
A | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+7507A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804954 | ||||||
chr14:96805141
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-6+7694T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805141 | ||||||
chr14:96805404
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+7957A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805404 | ||||||
chr14:96805422
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-6+7975C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805422 | ||||||
chr14:96805477
|
A | G | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+8030A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805477 | ||||||
chr14:96805651
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+8204C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805651 | ||||||
chr14:96805984
|
C | CT | 4 | a0001c0002t0001g0117a0001c0003t0001g0015a0001c0003t0001g0093others(1): Show | 5 | HG02970.hp1 HG02976.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8554dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | |||||
chr14:96805984
|
CT | C | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0002t0001g0118others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+8554delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | |||||
chr14:96805984
|
CTTTTTTT | C | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8548_-6+8554del others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | |||||
chr14:96805990
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02965.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+8543T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805990 | ||||||
chr14:96806045
|
T | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 76 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6+8598T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806045 | ||||||
chr14:96806067
|
C | T | 1 | a0001c0003t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-6+8620C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806067 | ||||||
chr14:96806216
|
C | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0096a0001c0002t0001g0097others(3): Show | 7 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+8769C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806216 | ||||||
chr14:96806227
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8780G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806227 | ||||||
chr14:96806292
|
C | T | 3 | a0001c0002t0001g0120a0001c0002t0001g0124a0001c0002t0001g0125 | 3 | NA18944.hp1 NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-6+8845C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806292 | ||||||
chr14:96806294
|
T | G | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6+8847T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806294 | ||||||
chr14:96806441
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-6+8994T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806441 | ||||||
chr14:96806622
|
C | T | 56 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(53): Show | 61 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6+9175C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806622 | ||||||
chr14:96806660
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+9213A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806660 | ||||||
chr14:96806740
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-6+9293A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806740 | ||||||
chr14:96806834
|
T | C | 1 | a0001c0003t0001g0015 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-6+9387T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806834 | ||||||
chr14:96807104
|
T | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0193a0001c0001t0001g0206others(11): Show | 15 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6+9657T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807104 | ||||||
chr14:96807115
|
C | T | 6 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG01192.hp1 HG01346.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+9668C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807115 | ||||||
chr14:96807165
|
G | T | 1 | a0001c0003t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-6+9718G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807165 | ||||||
chr14:96807264
|
C | T | 1 | a0001c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+9817C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807264 | ||||||
chr14:96807633
|
A | G | 6 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+10186A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807633 | ||||||
chr14:96807669
|
A | G | 4 | a0001c0003t0001g0075a0001c0003t0001g0076a0001c0003t0001g0077others(1): Show | 4 | HG02080.hp2 NA18964.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+10222A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807669 | ||||||
chr14:96807955
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-6+10508G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807955 | ||||||
chr14:96808002
|
C | CCTCTCTC others(21): Show |
2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(30): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(3): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0140 | 4 | HG01261.hp2 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(5): Show |
28 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(25): Show | 32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(7): Show |
1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6+10562_-6+10563i others(16): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(9): Show |
4 | a0001c0002t0001g0109a0001c0003t0001g0081a0001c0003t0001g0093others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(18): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(39): Show |
2 | a0001c0002t0001g0116a0001c0002t0001g0137 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(48): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(29): Show |
2 | a0001c0002t0001g0086a0001c0002t0001g0090 | 2 | HG02602.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(38): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(35): Show |
5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CCTCTCTC others(13): Show |
30 | a0001c0002t0001g0040a0001c0002t0001g0106a0001c0003t0001g0001others(27): Show | 37 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(22): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | |||||
chr14:96808002
|
C | CGTCTCTC others(1): Show |
6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | ||||||
chr14:96808002
|
C | CGTCTCTC others(35): Show |
2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | ||||||
chr14:96808002
|
C | CGTCTCTC others(3): Show |
3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | ||||||
chr14:96808002
|
C | CGTCTCTC others(5): Show |
4 | a0001c0002t0001g0033a0001c0002t0001g0036a0001c0003t0001g0092others(1): Show | 4 | HG02630.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | ||||||
chr14:96808002
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0035 | 2 | NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-6+10555C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | ||||||
chr14:96808003
|
C | CTCTCTCC others(27): Show |
2 | a0001c0002t0001g0017a0001c0002t0001g0087 | 3 | HG02572.hp1 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(36): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808003 | |||||
chr14:96808003
|
C | CTCTCTCC others(13): Show |
2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(22): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808003 | |||||
chr14:96808003
|
C | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10556C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808003 | ||||||
chr14:96808005
|
C | CTCTCCGT others(35): Show |
8 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(5): Show | 9 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808005 | |||||
chr14:96808007
|
C | CTCCGTCT others(23): Show |
3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG03098.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(32): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808007 | |||||
chr14:96808009
|
C | CCG | 25 | a0001c0003t0001g0002a0001c0003t0001g0013a0001c0003t0001g0014others(22): Show | 30 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808009 | ||||||
chr14:96808012
|
TCC | T | 7 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(4): Show | 8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10567_-6+10568d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808012 | |||||
chr14:96808014
|
C | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0017others(86): Show | 102 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.-6+10567C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808014 | ||||||
chr14:96808017
|
C | CTCTCTCT others(19): Show |
23 | a0001c0003t0001g0002a0001c0003t0001g0013a0001c0003t0001g0014others(20): Show | 28 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-6+10571_-6+10572i others(28): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTCTCTCT others(21): Show |
1 | a0001c0003t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-6+10571_-6+10572i others(30): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTCTCTCT others(23): Show |
1 | a0001c0003t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-6+10571_-6+10572i others(32): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTG | 9 | a0001c0002t0001g0105a0001c0002t0001g0106a0001c0002t0001g0107others(6): Show | 9 | HG01099.hp2 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10607_-6+10608d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTGTG | 7 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0083others(4): Show | 7 | HG02486.hp2 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+10605_-6+10608d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTGTGTG | 24 | a0001c0002t0001g0036a0001c0002t0001g0084a0001c0003t0001g0009others(21): Show | 29 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-6+10603_-6+10608d others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
C | CTGTGTGT others(3): Show |
1 | a0001c0002t0001g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-6+10599_-6+10608d others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
CTGTGTG | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG01099.hp1 HG03491.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10603_-6+10608d others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
CTGTGTGT others(1): Show |
C | 26 | a0001c0001t0001g0025a0001c0001t0001g0142a0001c0001t0001g0189others(23): Show | 27 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6+10601_-6+10608d others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
CTGTGTGT others(3): Show |
C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+10599_-6+10608d others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808017
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA18982.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-6+10597_-6+10608d others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | |||||
chr14:96808018
|
T | C | 24 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(21): Show | 25 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6+10571T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808018 | ||||||
chr14:96808019
|
G | C | 71 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0008others(68): Show | 80 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-6+10572G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808019 | ||||||
chr14:96808020
|
T | C | 2 | a0001c0002t0001g0040a0001c0002t0001g0123 | 2 | HG00733.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-6+10573T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808020 | ||||||
chr14:96808021
|
G | C | 71 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0008others(68): Show | 80 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-6+10574G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808021 | ||||||
chr14:96808022
|
T | C | 28 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(25): Show | 32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+10575T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808022 | ||||||
chr14:96808023
|
G | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0008others(44): Show | 55 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6+10576G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808023 | ||||||
chr14:96808024
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0140 | 4 | HG01261.hp2 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10577T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808024 | ||||||
chr14:96808025
|
G | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0008others(42): Show | 53 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.-6+10578G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808025 | ||||||
chr14:96808027
|
G | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0002t0001g0008others(14): Show | 21 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6+10580G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808027 | ||||||
chr14:96808028
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+10581T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808028 | ||||||
chr14:96808029
|
G | C | 15 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0026others(12): Show | 17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+10582G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808029 | ||||||
chr14:96808030
|
T | C | 7 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(4): Show | 8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10583T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808030 | ||||||
chr14:96808031
|
G | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10584G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808031 | ||||||
chr14:96808033
|
G | C | 7 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(4): Show | 8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10586G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808033 | ||||||
chr14:96808054
|
T | C | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+10607T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808054 | ||||||
chr14:96808057
|
A | G | 31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+10610A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808057 | ||||||
chr14:96808091
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6+10644G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808091 | ||||||
chr14:96808117
|
G | A | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+10670G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808117 | ||||||
chr14:96808264
|
T | C | 12 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(9): Show | 12 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+10817T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808264 | ||||||
chr14:96808415
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-6+10968G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808415 | ||||||
chr14:96808433
|
G | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 267 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.-6+10986G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808433 | ||||||
chr14:96808658
|
C | CT | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0002t0001g0244others(2): Show | 5 | HG00738.hp1 HG01261.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+11228dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808658 | |||||
chr14:96808658
|
CTTTTT | C | 38 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0020others(35): Show | 43 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6+11224_-6+11228d others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808658 | |||||
chr14:96808910
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+11463C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808910 | ||||||
chr14:96808919
|
A | G | 130 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(127): Show | 148 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.-6+11472A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808919 | ||||||
chr14:96809012
|
G | A | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11565G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809012 | ||||||
chr14:96809230
|
C | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11783C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809230 | ||||||
chr14:96809384
|
C | G | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+11937C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809384 | ||||||
chr14:96809548
|
A | AGCTT | 115 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(112): Show | 132 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.-6+12118_-6+12121d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809548 | |||||
chr14:96809569
|
T | G | 29 | a0001c0001t0001g0202a0001c0002t0001g0019a0001c0002t0001g0031others(26): Show | 30 | HG00140.hp2 HG01109.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.-6+12122T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809569 | ||||||
chr14:96809570
|
C | CT | 11 | a0001c0001t0001g0186a0001c0001t0001g0225a0001c0002t0001g0008others(8): Show | 12 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+12141dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809570 | |||||
chr14:96809571
|
T | TTTC | 7 | a0001c0002t0001g0088a0001c0002t0001g0242a0001c0002t0001g0243others(4): Show | 7 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+12126_-6+12127i others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809571 | |||||
chr14:96809668
|
G | A | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+12221G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809668 | ||||||
chr14:96809950
|
A | C | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+12503A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809950 | ||||||
chr14:96810330
|
A | G | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+12883A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810330 | ||||||
chr14:96810352
|
C | T | 2 | a0001c0001t0001g0185a0001c0003t0001g0014 | 3 | HG01256.hp1 HG01258.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-6+12905C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810352 | ||||||
chr14:96810668
|
C | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 80 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6+13221C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810668 | ||||||
chr14:96810683
|
A | C | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+13236A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810683 | ||||||
chr14:96810704
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-6+13257G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810704 | ||||||
chr14:96810786
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+13339T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810786 | ||||||
chr14:96810837
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-6+13390T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810837 | ||||||
chr14:96810858
|
T | C | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-6+13411T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810858 | ||||||
chr14:96810894
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0194 | 4 | HG01891.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+13447T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810894 | ||||||
chr14:96810933
|
A | AT | 34 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(31): Show | 38 | HG01071.hp2 HG01074.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.-6+13497dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810933 | |||||
chr14:96810933
|
AT | A | 62 | a0001c0002t0001g0040a0001c0002t0001g0083a0001c0002t0001g0084others(59): Show | 74 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-6+13497delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810933 | |||||
chr14:96810960
|
T | TG | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+13515dupG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810960 | |||||
chr14:96811032
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-6+13585C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811032 | ||||||
chr14:96811086
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+13639C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811086 | ||||||
chr14:96811105
|
A | G | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+13658A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811105 | ||||||
chr14:96811188
|
C | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-6+13741C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811188 | ||||||
chr14:96811284
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02818.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-6+13837T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811284 | ||||||
chr14:96811348
|
G | A | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+13901G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811348 | ||||||
chr14:96811410
|
A | G | 1 | a0001c0003t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-6+13963A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811410 | ||||||
chr14:96811485
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+14038A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811485 | ||||||
chr14:96811537
|
G | A | 61 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(58): Show | 73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-6+14090G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811537 | ||||||
chr14:96811585
|
A | C | 31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+14138A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811585 | ||||||
chr14:96811628
|
G | C | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+14181G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811628 | ||||||
chr14:96811685
|
T | G | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-6+14238T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811685 | ||||||
chr14:96811755
|
A | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-6+14308A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811755 | ||||||
chr14:96811773
|
C | CT | 135 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(132): Show | 154 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.-6+14337dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96811773 | |||||
chr14:96811915
|
A | G | 1 | a0001c0002t0003g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-6+14468A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811915 | ||||||
chr14:96811993
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-6+14546G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811993 | ||||||
chr14:96812315
|
C | T | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-6+14868C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812315 | ||||||
chr14:96812381
|
G | T | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+14934G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812381 | ||||||
chr14:96812808
|
T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+15361T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812808 | ||||||
chr14:96812811
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-6+15364A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812811 | ||||||
chr14:96812834
|
C | T | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+15387C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812834 | ||||||
chr14:96812883
|
T | C | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-6+15436T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812883 | ||||||
chr14:96812957
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+15510G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812957 | ||||||
chr14:96813120
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-6+15673C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813120 | ||||||
chr14:96813590
|
C | T | 1 | a0001c0003t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6+16143C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813590 | ||||||
chr14:96813703
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6+16256A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813703 | ||||||
chr14:96813784
|
A | G | 12 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(9): Show | 13 | HG02145.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6+16337A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813784 | ||||||
chr14:96813857
|
T | G | 1 | a0001c0002t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+16410T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813857 | ||||||
chr14:96813880
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-6+16433G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813880 | ||||||
chr14:96814003
|
A | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+16556A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814003 | ||||||
chr14:96814037
|
G | A | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+16590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814037 | ||||||
chr14:96814288
|
G | GATCA | 2 | a0001c0003t0001g0009a0001c0003t0001g0041 | 3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+16841_-6+16842i others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814288 | ||||||
chr14:96814291
|
T | C | 2 | a0001c0003t0001g0009a0001c0003t0001g0041 | 3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+16844T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814291 | ||||||
chr14:96814341
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+16894A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814341 | ||||||
chr14:96814647
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+17200G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814647 | ||||||
chr14:96814681
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-6+17234C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814681 | ||||||
chr14:96814908
|
C | T | 101 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(98): Show | 117 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.-6+17461C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814908 | ||||||
chr14:96814919
|
A | G | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+17472A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814919 | ||||||
chr14:96815009
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+17562G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815009 | ||||||
chr14:96815410
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+17963G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815410 | ||||||
chr14:96815474
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-17993C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815474 | ||||||
chr14:96815823
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-5-17644G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815823 | ||||||
chr14:96815965
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5-17502G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815965 | ||||||
chr14:96816015
|
A | T | 2 | a0001c0003t0001g0016a0001c0003t0001g0082 | 3 | HG01069.hp2 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-5-17452A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816015 | ||||||
chr14:96816098
|
T | C | 36 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(33): Show | 40 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-5-17369T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816098 | ||||||
chr14:96816175
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0117 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-5-17292C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816175 | ||||||
chr14:96816209
|
G | A | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-17258G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816209 | ||||||
chr14:96816230
|
G | A | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-17237G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816230 | ||||||
chr14:96816436
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5-17031C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816436 | ||||||
chr14:96816765
|
TGAC | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-16701_-5-16699d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816765 | ||||||
chr14:96817158
|
C | T | 138 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(135): Show | 157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-16309C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817158 | ||||||
chr14:96817186
|
G | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-16281G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817186 | ||||||
chr14:96817276
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 76 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-5-16191T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817276 | ||||||
chr14:96817349
|
T | C | 138 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(135): Show | 157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-16118T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817349 | ||||||
chr14:96817612
|
T | C | 6 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 7 | HG02055.hp2 HG02109.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-15855T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817612 | ||||||
chr14:96817708
|
A | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-15759A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817708 | ||||||
chr14:96817744
|
C | A | 1 | a0001c0002t0001g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-15723C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817744 | ||||||
chr14:96817883
|
A | T | 1 | a0001c0002t0001g0022 | 2 | NA18991.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-5-15584A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817883 | ||||||
chr14:96817898
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-5-15569G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817898 | ||||||
chr14:96818064
|
T | TGGATCCT others(300): Show |
1 | a0001c0002t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5-15100_-5-15099i others(309): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96818064 | |||||
chr14:96818169
|
G | GCTTGTGT others(300): Show |
2 | a0001c0002t0001g0083a0001c0002t0001g0085 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-15100_-5-15099i others(309): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96818169 | |||||
chr14:96818416
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5-15051A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818416 | ||||||
chr14:96818903
|
G | T | 1 | a0001c0003t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5-14564G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818903 | ||||||
chr14:96818956
|
A | G | 6 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-14511A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818956 | ||||||
chr14:96818981
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-14486C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818981 | ||||||
chr14:96818988
|
G | A | 1 | a0001c0003t0001g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-5-14479G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818988 | ||||||
chr14:96819094
|
T | A | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-5-14373T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819094 | ||||||
chr14:96819147
|
A | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-14320A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819147 | ||||||
chr14:96819284
|
C | G | 1 | a0001c0002t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-5-14183C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819284 | ||||||
chr14:96819333
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-14134A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819333 | ||||||
chr14:96819429
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-5-14038C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819429 | ||||||
chr14:96819542
|
G | A | 3 | a0001c0001t0001g0152a0001c0002t0001g0128a0001c0003t0001g0059 | 3 | HG01978.hp2 NA18943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-5-13925G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819542 | ||||||
chr14:96819768
|
A | G | 138 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(135): Show | 157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-13699A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819768 | ||||||
chr14:96819807
|
C | T | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-13660C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819807 | ||||||
chr14:96819914
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5-13553C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819914 | ||||||
chr14:96820152
|
C | CT | 132 | a0001c0002t0001g0008a0001c0002t0001g0018a0001c0002t0001g0019others(129): Show | 150 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.-5-13312dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96820152 | |||||
chr14:96820167
|
G | A | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-13300G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820167 | ||||||
chr14:96820273
|
T | C | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-13194T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820273 | ||||||
chr14:96820393
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-13074A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820393 | ||||||
chr14:96820443
|
C | T | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-13024C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820443 | ||||||
chr14:96820536
|
T | G | 6 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(3): Show | 7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-12931T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820536 | ||||||
chr14:96820570
|
G | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12897G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820570 | ||||||
chr14:96820653
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5-12814G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820653 | ||||||
chr14:96820685
|
T | C | 15 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(12): Show | 16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-12782T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820685 | ||||||
chr14:96820705
|
C | T | 1 | a0001c0003t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-5-12762C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820705 | ||||||
chr14:96820773
|
A | G | 6 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-12694A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820773 | ||||||
chr14:96820803
|
T | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12664T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820803 | ||||||
chr14:96820910
|
A | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0087 | 3 | HG02572.hp1 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-5-12557A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820910 | ||||||
chr14:96821176
|
T | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-12291T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821176 | ||||||
chr14:96821237
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12230G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821237 | ||||||
chr14:96821315
|
C | T | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-12152C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821315 | ||||||
chr14:96821387
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-5-12080C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821387 | ||||||
chr14:96821413
|
G | A | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-5-12054G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821413 | ||||||
chr14:96821422
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-5-12045C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821422 | ||||||
chr14:96821437
|
T | TA | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-12022dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821437 | |||||
chr14:96821448
|
A | G | 1 | a0001c0002t0001g0019 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-5-12019A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821448 | ||||||
chr14:96821500
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-5-11967T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821500 | ||||||
chr14:96821551
|
T | C | 1 | a0001c0003t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5-11916T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821551 | ||||||
chr14:96821633
|
G | A | 133 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(130): Show | 152 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-5-11834G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821633 | ||||||
chr14:96821655
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5-11812A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821655 | ||||||
chr14:96821674
|
G | A | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-11793G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821674 | ||||||
chr14:96821899
|
C | A | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-11568C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821899 | ||||||
chr14:96821969
|
C | CT | 76 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0213others(73): Show | 89 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-5-11483dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821969 | |||||
chr14:96821969
|
CT | C | 13 | a0001c0001t0001g0154a0001c0002t0001g0006a0001c0002t0001g0019others(10): Show | 16 | HG01071.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-11483delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821969 | |||||
chr14:96822080
|
C | CT | 6 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(3): Show | 7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-11374dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822080 | |||||
chr14:96822080
|
CT | C | 69 | a0001c0002t0001g0008a0001c0002t0001g0019a0001c0002t0001g0026others(66): Show | 83 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-5-11374delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822080 | |||||
chr14:96822397
|
C | A | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-11070C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822397 | ||||||
chr14:96822402
|
A | AGTT | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-11063_-5-11061d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822402 | |||||
chr14:96822466
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-11001G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822466 | ||||||
chr14:96822686
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-5-10781C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822686 | ||||||
chr14:96822756
|
A | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-10711A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822756 | ||||||
chr14:96823377
|
C | T | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-10090C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823377 | ||||||
chr14:96823455
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-5-10012T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823455 | ||||||
chr14:96823670
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-5-9797G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823670 | ||||||
chr14:96823739
|
C | T | 26 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-9728C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823739 | ||||||
chr14:96823789
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-9678G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823789 | ||||||
chr14:96823953
|
T | C | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-5-9514T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823953 | ||||||
chr14:96823992
|
G | A | 47 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0020others(44): Show | 52 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-5-9475G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823992 | ||||||
chr14:96824208
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-9259A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824208 | ||||||
chr14:96824289
|
A | G | 1 | a0001c0002t0001g0132 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5-9178A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824289 | ||||||
chr14:96824306
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5-9161G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824306 | ||||||
chr14:96824329
|
A | G | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-9138A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824329 | ||||||
chr14:96824462
|
A | G | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-9005A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824462 | ||||||
chr14:96824574
|
C | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-8893C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824574 | ||||||
chr14:96824575
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-8892G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824575 | ||||||
chr14:96824662
|
T | A | 1 | a0001c0002t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-5-8805T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824662 | ||||||
chr14:96824665
|
A | AT | 9 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0088others(6): Show | 10 | HG00558.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5-8784dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96824665 | |||||
chr14:96824665
|
AT | A | 35 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0002t0001g0018others(32): Show | 39 | HG00140.hp1 HG00733.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-5-8784delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96824665 | |||||
chr14:96824693
|
G | A | 6 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(3): Show | 6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-8774G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824693 | ||||||
chr14:96824725
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-8742C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824725 | ||||||
chr14:96824727
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-5-8740C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824727 | ||||||
chr14:96824763
|
C | T | 3 | a0001c0002t0001g0008a0001c0002t0001g0030a0001c0002t0001g0032 | 4 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8704C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824763 | ||||||
chr14:96824938
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0103 | 2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-8529C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824938 | ||||||
chr14:96825458
|
C | G | 15 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(12): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-8009C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825458 | ||||||
chr14:96825512
|
T | C | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-7955T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825512 | ||||||
chr14:96825695
|
A | G | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-7772A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825695 | ||||||
chr14:96825752
|
T | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0232 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-5-7715T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825752 | ||||||
chr14:96825780
|
C | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7687C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825780 | ||||||
chr14:96825800
|
A | G | 15 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(12): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-7667A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825800 | ||||||
chr14:96825860
|
T | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-7607T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825860 | ||||||
chr14:96825905
|
T | G | 61 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(58): Show | 73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5-7562T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825905 | ||||||
chr14:96825994
|
G | GT | 20 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0016others(17): Show | 23 | HG00438.hp1 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-7472dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96825994 | |||||
chr14:96826060
|
T | C | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-7407T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826060 | ||||||
chr14:96826182
|
C | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7285C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826182 | ||||||
chr14:96826276
|
G | T | 3 | a0001c0002t0001g0018a0001c0002t0001g0096a0001c0002t0001g0097 | 4 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-7191G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826276 | ||||||
chr14:96826284
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-7183A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826284 | ||||||
chr14:96826636
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 79 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.-5-6831C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826636 | ||||||
chr14:96826637
|
G | A | 133 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(130): Show | 152 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-5-6830G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826637 | ||||||
chr14:96826673
|
G | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-6794G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826673 | ||||||
chr14:96826855
|
C | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-6612C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826855 | ||||||
chr14:96826877
|
T | C | 62 | a0001c0002t0001g0040a0001c0002t0001g0083a0001c0002t0001g0084others(59): Show | 74 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-5-6590T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826877 | ||||||
chr14:96827139
|
T | TTC | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-5-6326_-5-6325dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96827139 | |||||
chr14:96827257
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5-6210A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827257 | ||||||
chr14:96827376
|
A | G | 133 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(130): Show | 152 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-5-6091A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827376 | ||||||
chr14:96827396
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-6071G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827396 | ||||||
chr14:96827404
|
G | T | 3 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113 | 3 | HG02055.hp2 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-5-6063G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827404 | ||||||
chr14:96827426
|
G | C | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-6041G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827426 | ||||||
chr14:96827505
|
G | A | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-5962G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827505 | ||||||
chr14:96827566
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-5-5901C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827566 | ||||||
chr14:96827622
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0226 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5-5845C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827622 | ||||||
chr14:96827669
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-5798C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827669 | ||||||
chr14:96827675
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-5-5792C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827675 | ||||||
chr14:96827682
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-5785A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827682 | ||||||
chr14:96827818
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-5-5649G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827818 | ||||||
chr14:96827860
|
A | G | 58 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(55): Show | 70 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-5-5607A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827860 | ||||||
chr14:96827946
|
T | C | 77 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(74): Show | 90 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-5-5521T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827946 | ||||||
chr14:96827963
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0103 | 2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-5504C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827963 | ||||||
chr14:96828017
|
G | C | 1 | a0001c0003t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-5-5450G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828017 | ||||||
chr14:96828130
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-5-5337C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828130 | ||||||
chr14:96828155
|
CTGT | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 109 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-5-5306_-5-5304del others(3): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96828155 | |||||
chr14:96828164
|
G | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-5303G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828164 | ||||||
chr14:96828383
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 123 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-5-5084T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828383 | ||||||
chr14:96828424
|
T | G | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-5043T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828424 | ||||||
chr14:96828468
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-5-4999T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828468 | ||||||
chr14:96828568
|
A | G | 1 | a0001c0002t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-5-4899A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828568 | ||||||
chr14:96828598
|
A | G | 76 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(73): Show | 89 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-5-4869A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828598 | ||||||
chr14:96828653
|
TA | T | 26 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-4807delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96828653 | |||||
chr14:96828702
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-5-4765G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828702 | ||||||
chr14:96828796
|
G | A | 15 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(12): Show | 16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-4671G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828796 | ||||||
chr14:96828823
|
C | T | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5-4644C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828823 | ||||||
chr14:96829206
|
A | AT | 14 | a0001c0001t0001g0202a0001c0002t0001g0135a0001c0002t0001g0136others(11): Show | 14 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5-4244dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96829206 | |||||
chr14:96829206
|
AT | A | 15 | a0001c0001t0001g0141a0001c0001t0001g0220a0001c0002t0001g0033others(12): Show | 15 | HG01074.hp2 HG01981.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-4244delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96829206 | |||||
chr14:96829277
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-4190A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829277 | ||||||
chr14:96829282
|
T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-4185T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829282 | ||||||
chr14:96829294
|
G | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4173G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829294 | ||||||
chr14:96829444
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-5-4023A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829444 | ||||||
chr14:96829469
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5-3998G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829469 | ||||||
chr14:96829544
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0232 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-5-3923A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829544 | ||||||
chr14:96829734
|
C | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-3733C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829734 | ||||||
chr14:96829957
|
T | A | 1 | a0001c0003t0001g0054 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-5-3510T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829957 | ||||||
chr14:96830059
|
CT | C | 59 | a0001c0001t0001g0160a0001c0003t0001g0001a0001c0003t0001g0002others(56): Show | 71 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.-5-3407delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830059 | ||||||
chr14:96830177
|
G | C | 1 | a0001c0002t0001g0129 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-5-3290G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830177 | ||||||
chr14:96830394
|
C | T | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-3073C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830394 | ||||||
chr14:96830416
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-3051G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830416 | ||||||
chr14:96830451
|
C | G | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-3016C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830451 | ||||||
chr14:96830615
|
A | G | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-2852A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830615 | ||||||
chr14:96830761
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0188a0001c0001t0001g0190 | 3 | HG02027.hp1 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-5-2706G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830761 | ||||||
chr14:96831008
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-2459C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831008 | ||||||
chr14:96831213
|
G | A | 2 | a0001c0003t0001g0056a0001c0003t0001g0061 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-5-2254G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831213 | ||||||
chr14:96831261
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-5-2206G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831261 | ||||||
chr14:96831329
|
T | C | 1 | a0001c0003t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-5-2138T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831329 | ||||||
chr14:96831433
|
T | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-2034T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831433 | ||||||
chr14:96831464
|
T | C | 1 | a0001c0003t0001g0062 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-5-2003T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831464 | ||||||
chr14:96831488
|
C | T | 3 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036 | 3 | HG03942.hp2 NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-5-1979C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831488 | ||||||
chr14:96831816
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-1651G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831816 | ||||||
chr14:96832032
|
CTT | C | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-1432_-5-1431del others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96832032 | |||||
chr14:96832060
|
T | G | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-5-1407T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832060 | ||||||
chr14:96832121
|
TA | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 275 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.-5-1341delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96832121 | |||||
chr14:96832158
|
G | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-1309G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832158 | ||||||
chr14:96832199
|
G | C | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-1268G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832199 | ||||||
chr14:96832315
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-5-1152A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832315 | ||||||
chr14:96832351
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-5-1116C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832351 | ||||||
chr14:96832353
|
A | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-1114A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832353 | ||||||
chr14:96832588
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-879G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832588 | ||||||
chr14:96832715
|
A | G | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-5-752A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832715 | ||||||
chr14:96832773
|
C | CTTGCCCA others(6): Show |
3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-694_-5-693insTT others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832773 | ||||||
chr14:96832774
|
A | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-693A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832774 | ||||||
chr14:96832775
|
C | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-692C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832775 | ||||||
chr14:96833067
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5-400T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833067 | ||||||
chr14:96833080
|
C | T | 54 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(51): Show | 66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-5-387C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833080 | ||||||
chr14:96833254
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-213G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833254 | ||||||
chr14:96833692
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160+61G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833692 | ||||||
chr14:96833705
|
T | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+74T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833705 | ||||||
chr14:96833861
|
G | C | 1 | a0001c0003t0001g0011 | 2 | NA18945.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.160+230G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833861 | ||||||
chr14:96833928
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+297G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833928 | ||||||
chr14:96834016
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+385G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834016 | ||||||
chr14:96834149
|
C | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.160+518C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834149 | ||||||
chr14:96834195
|
T | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+564T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834195 | ||||||
chr14:96834386
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.160+755C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834386 | ||||||
chr14:96834404
|
C | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+773C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834404 | ||||||
chr14:96834506
|
A | T | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+875A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834506 | ||||||
chr14:96834511
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0231 | 2 | NA18962.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.160+880T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834511 | ||||||
chr14:96834530
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.160+899C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834530 | ||||||
chr14:96834669
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+1038A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834669 | ||||||
chr14:96834782
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+1151A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834782 | ||||||
chr14:96834903
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160+1272A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834903 | ||||||
chr14:96834910
|
C | G | 28 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(25): Show | 32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.160+1279C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834910 | ||||||
chr14:96834993
|
G | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.160+1362G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834993 | ||||||
chr14:96835147
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+1516G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835147 | ||||||
chr14:96835187
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.160+1556A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835187 | ||||||
chr14:96835497
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.160+1866C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835497 | ||||||
chr14:96835743
|
A | G | 3 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0003t0001g0041 | 3 | HG00642.hp2 HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.161-2019A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835743 | ||||||
chr14:96835889
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-1873A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835889 | ||||||
chr14:96835937
|
C | T | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.161-1825C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835937 | ||||||
chr14:96835938
|
G | A | 1 | a0001c0003t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161-1824G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835938 | ||||||
chr14:96836127
|
A | T | 17 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(14): Show | 18 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-1635A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836127 | ||||||
chr14:96836518
|
C | CT | 5 | a0001c0001t0001g0024a0001c0001t0001g0152a0001c0001t0001g0207others(2): Show | 6 | HG01168.hp2 HG01978.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-1222dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | |||||
chr14:96836518
|
CT | C | 90 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0002t0001g0008others(87): Show | 105 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.161-1222delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | |||||
chr14:96836518
|
CTT | C | 17 | a0001c0002t0001g0018a0001c0002t0001g0040a0001c0002t0001g0083others(14): Show | 18 | HG00733.hp1 HG01074.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-1223_161-1222d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | |||||
chr14:96836518
|
CTTTTT | C | 16 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(13): Show | 19 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-1226_161-1222d others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | |||||
chr14:96836717
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-1045G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836717 | ||||||
chr14:96836778
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.161-984G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836778 | ||||||
chr14:96837243
|
C | T | 1 | a0001c0003t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-519C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837243 | ||||||
chr14:96837268
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-494G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837268 | ||||||
chr14:96837451
|
T | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01168.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.161-311T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837451 | ||||||
chr14:96837479
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-283C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837479 | ||||||
chr14:96837542
|
A | G | 55 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(52): Show | 67 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-220A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837542 | ||||||
chr14:96837617
|
A | G | 62 | a0001c0002t0001g0040a0001c0002t0001g0083a0001c0002t0001g0084others(59): Show | 74 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.161-145A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837617 | ||||||
chr14:96837688
|
A | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-74A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837688 | ||||||
chr14:96837741
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.161-21A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837741 | ||||||
chr14:96837836
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.216+19A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96837836 | ||||||
chr14:96838116
|
T | C | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.216+299T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838116 | ||||||
chr14:96838223
|
G | GTTTA | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+408_216+409ins others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96838223 | |||||
chr14:96838358
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+541C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838358 | ||||||
chr14:96838571
|
T | TA | 57 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(54): Show | 69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.216+754_216+755ins others(1): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838571 | ||||||
chr14:96838571
|
T | TC | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 208 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.216+755dupC | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96838571 | |||||
chr14:96838664
|
C | T | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+847C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838664 | ||||||
chr14:96838743
|
A | C | 1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.216+926A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838743 | ||||||
chr14:96838770
|
C | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 275 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.216+953C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838770 | ||||||
chr14:96838799
|
C | T | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+982C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838799 | ||||||
chr14:96838856
|
C | G | 1 | a0001c0002t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.216+1039C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838856 | ||||||
chr14:96838874
|
A | C | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.216+1057A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838874 | ||||||
chr14:96838916
|
CATAG | C | 57 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(54): Show | 69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.216+1103_216+1106d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96838916 | |||||
chr14:96839062
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.216+1245T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839062 | ||||||
chr14:96839084
|
G | GT | 21 | a0001c0001t0001g0138a0001c0001t0001g0176a0001c0001t0001g0177others(18): Show | 22 | HG00735.hp1 HG01361.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.216+1286dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | |||||
chr14:96839084
|
G | GTT | 36 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(33): Show | 40 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.216+1285_216+1286d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | |||||
chr14:96839084
|
G | GTTT | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+1284_216+1286d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | |||||
chr14:96839295
|
A | T | 1 | a0001c0003t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.216+1478A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839295 | ||||||
chr14:96839318
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.216+1501G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839318 | ||||||
chr14:96839376
|
CT | C | 57 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(54): Show | 69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.216+1560delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839376 | ||||||
chr14:96839464
|
ATAATATA others(2): Show |
A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216+1648_216+1656d others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839464 | ||||||
chr14:96839548
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1731G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839548 | ||||||
chr14:96839558
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+1741G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839558 | ||||||
chr14:96839571
|
T | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+1754T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839571 | ||||||
chr14:96839589
|
T | A | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.216+1772T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839589 | ||||||
chr14:96839679
|
C | G | 1 | a0001c0002t0001g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.216+1862C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839679 | ||||||
chr14:96839923
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.216+2106C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839923 | ||||||
chr14:96840049
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.216+2232T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840049 | ||||||
chr14:96840147
|
C | A | 1 | a0001c0003t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.216+2330C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840147 | ||||||
chr14:96840252
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.216+2435G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840252 | ||||||
chr14:96840372
|
G | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216+2555G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840372 | ||||||
chr14:96840464
|
T | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2647T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840464 | ||||||
chr14:96840469
|
T | C | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2652T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840469 | ||||||
chr14:96840552
|
A | T | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+2735A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840552 | ||||||
chr14:96840573
|
T | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.216+2756T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840573 | ||||||
chr14:96840601
|
A | G | 55 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(52): Show | 67 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.216+2784A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840601 | ||||||
chr14:96840681
|
A | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+2864A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840681 | ||||||
chr14:96840801
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.216+2984A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840801 | ||||||
chr14:96840834
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.216+3017C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840834 | ||||||
chr14:96840858
|
C | CT | 37 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0159others(34): Show | 39 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.216+3056dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96840858 | |||||
chr14:96840858
|
CT | C | 43 | a0001c0001t0001g0146a0001c0002t0001g0018a0001c0002t0001g0020others(40): Show | 47 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.216+3056delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96840858 | |||||
chr14:96840875
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+3058A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840875 | ||||||
chr14:96840887
|
A | G | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.216+3070A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840887 | ||||||
chr14:96841006
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0216 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.216+3189C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841006 | ||||||
chr14:96841016
|
C | T | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.216+3199C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841016 | ||||||
chr14:96841151
|
C | T | 2 | a0001c0003t0001g0074a0001c0003t0001g0080 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.216+3334C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841151 | ||||||
chr14:96841749
|
C | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+3932C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841749 | ||||||
chr14:96841834
|
C | CA | 33 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(30): Show | 37 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.216+4031dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96841834 | |||||
chr14:96841934
|
C | T | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+4117C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841934 | ||||||
chr14:96841957
|
A | G | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.217-4138A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841957 | ||||||
chr14:96841965
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.217-4130C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841965 | ||||||
chr14:96841995
|
A | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.217-4100A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841995 | ||||||
chr14:96842209
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0175 | 2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.217-3886A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842209 | ||||||
chr14:96842343
|
A | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3752A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842343 | ||||||
chr14:96842490
|
G | C | 1 | a0001c0002t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.217-3605G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842490 | ||||||
chr14:96842632
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.217-3463G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842632 | ||||||
chr14:96843011
|
C | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-3084C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843011 | ||||||
chr14:96843089
|
A | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.217-3006A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843089 | ||||||
chr14:96843150
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.217-2945C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843150 | ||||||
chr14:96843242
|
A | G | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-2853A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843242 | ||||||
chr14:96843417
|
T | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-2678T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843417 | ||||||
chr14:96844091
|
T | C | 15 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(12): Show | 16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-2004T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844091 | ||||||
chr14:96844298
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0173others(4): Show | 7 | HG00639.hp2 HG01257.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-1797A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844298 | ||||||
chr14:96844560
|
G | T | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1535G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844560 | ||||||
chr14:96844592
|
A | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.217-1503A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844592 | ||||||
chr14:96844763
|
A | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-1332A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844763 | ||||||
chr14:96844826
|
C | T | 6 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(3): Show | 6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1269C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844826 | ||||||
chr14:96844876
|
T | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-1219T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844876 | ||||||
chr14:96844877
|
A | G | 6 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(3): Show | 6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1218A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844877 | ||||||
chr14:96844917
|
G | T | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.217-1178G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844917 | ||||||
chr14:96844984
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-1111C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844984 | ||||||
chr14:96844990
|
A | G | 1 | a0001c0003t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.217-1105A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844990 | ||||||
chr14:96845211
|
C | CT | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 114 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.217-877dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96845211 | |||||
chr14:96845211
|
C | CTT | 134 | a0001c0001t0001g0222a0001c0002t0001g0008a0001c0002t0001g0017others(131): Show | 153 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.217-878_217-877dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96845211 | |||||
chr14:96845356
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0116 | 4 | HG02895.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-739A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845356 | ||||||
chr14:96845523
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-572A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845523 | ||||||
chr14:96845557
|
G | A | 6 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(3): Show | 6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-538G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845557 | ||||||
chr14:96845563
|
T | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-532T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845563 | ||||||
chr14:96845630
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-465C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845630 | ||||||
chr14:96845812
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.217-283T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845812 | ||||||
chr14:96845851
|
T | C | 61 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(58): Show | 73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.217-244T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845851 | ||||||
chr14:96846209
|
G | GT | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+51dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846209 | |||||
chr14:96846257
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.286+93C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846257 | ||||||
chr14:96846276
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.286+112T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846276 | ||||||
chr14:96846305
|
G | A | 140 | a0001c0001t0001g0222a0001c0002t0001g0008a0001c0002t0001g0017others(137): Show | 159 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.286+141G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846305 | ||||||
chr14:96846628
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+464G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846628 | ||||||
chr14:96846642
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0172 | 5 | HG01891.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+478A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846642 | ||||||
chr14:96846643
|
G | GGATA | 32 | a0001c0001t0001g0222a0001c0002t0001g0018a0001c0002t0001g0020others(29): Show | 36 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.286+481_286+484dup others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846643 | |||||
chr14:96846714
|
GA | G | 17 | a0001c0001t0001g0208a0001c0002t0001g0019a0001c0002t0001g0104others(14): Show | 18 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-531delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846714 | |||||
chr14:96846727
|
G | A | 1 | a0001c0003t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-530G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846727 | ||||||
chr14:96846733
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.287-524A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846733 | ||||||
chr14:96846821
|
A | G | 10 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(7): Show | 11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-436A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846821 | ||||||
chr14:96846837
|
A | G | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.287-420A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846837 | ||||||
chr14:96846841
|
A | G | 1 | a0001c0002t0001g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.287-416A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846841 | ||||||
chr14:96846914
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.287-343G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846914 | ||||||
chr14:96847065
|
G | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-192G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847065 | ||||||
chr14:96847071
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.287-186T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847071 | ||||||
chr14:96847103
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.287-154C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847103 | ||||||
chr14:96847433
|
T | TA | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.374+90dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96847433 | |||||
chr14:96847548
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.374+204T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847548 | ||||||
chr14:96847614
|
A | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.374+270A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847614 | ||||||
chr14:96847647
|
T | TC | 26 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+305dupC | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96847647 | |||||
chr14:96847833
|
T | C | 21 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(18): Show | 22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.374+489T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847833 | ||||||
chr14:96847836
|
A | G | 55 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(52): Show | 67 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.374+492A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847836 | ||||||
chr14:96848168
|
T | G | 26 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+824T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848168 | ||||||
chr14:96848264
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.374+920A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848264 | ||||||
chr14:96848267
|
G | A | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.374+923G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848267 | ||||||
chr14:96848442
|
C | T | 13 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(10): Show | 13 | HG02630.hp1 HG02886.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.374+1098C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848442 | ||||||
chr14:96848456
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.374+1112C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848456 | ||||||
chr14:96848627
|
T | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.374+1283T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848627 | ||||||
chr14:96848894
|
T | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.374+1550T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848894 | ||||||
chr14:96848906
|
A | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.374+1562A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848906 | ||||||
chr14:96849023
|
G | A | 61 | a0001c0002t0001g0040a0001c0002t0001g0083a0001c0002t0001g0084others(58): Show | 73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.374+1679G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849023 | ||||||
chr14:96849086
|
C | T | 26 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+1742C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849086 | ||||||
chr14:96849183
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.374+1839G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849183 | ||||||
chr14:96849199
|
C | T | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.374+1855C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849199 | ||||||
chr14:96849448
|
T | TA | 16 | a0001c0002t0001g0019a0001c0002t0001g0105a0001c0002t0001g0106others(13): Show | 17 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.374+2116dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96849448 | |||||
chr14:96849573
|
T | C | 21 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(18): Show | 22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.374+2229T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849573 | ||||||
chr14:96849691
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0156a0001c0001t0001g0171others(1): Show | 5 | NA18944.hp2 NA18977.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+2347C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849691 | ||||||
chr14:96849765
|
G | T | 139 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(136): Show | 158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.374+2421G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849765 | ||||||
chr14:96849864
|
C | A | 1 | a0001c0002t0001g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.374+2520C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849864 | ||||||
chr14:96849995
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+2651G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849995 | ||||||
chr14:96850044
|
C | T | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.374+2700C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850044 | ||||||
chr14:96850210
|
T | C | 9 | a0001c0002t0001g0019a0001c0002t0001g0110a0001c0002t0001g0111others(6): Show | 10 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.375-2621T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850210 | ||||||
chr14:96850242
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.375-2589A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850242 | ||||||
chr14:96850251
|
A | G | 17 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(14): Show | 18 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-2580A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850251 | ||||||
chr14:96850490
|
G | A | 3 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244 | 3 | HG02145.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.375-2341G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850490 | ||||||
chr14:96850609
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.375-2222A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850609 | ||||||
chr14:96850736
|
A | G | 1 | a0001c0003t0001g0054 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.375-2095A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850736 | ||||||
chr14:96850966
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.375-1865C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850966 | ||||||
chr14:96850980
|
A | G | 2 | a0001c0003t0001g0037a0001c0003t0001g0038 | 2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.375-1851A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850980 | ||||||
chr14:96851001
|
G | A | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.375-1830G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851001 | ||||||
chr14:96851062
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375-1769A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851062 | ||||||
chr14:96851261
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.375-1570C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851261 | ||||||
chr14:96851295
|
C | T | 3 | a0001c0001t0001g0222a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.375-1536C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851295 | ||||||
chr14:96851390
|
C | T | 8 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0159others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.375-1441C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851390 | ||||||
chr14:96851548
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.375-1283C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851548 | ||||||
chr14:96851586
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 108 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.375-1245A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851586 | ||||||
chr14:96851615
|
T | C | 17 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(14): Show | 18 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-1216T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851615 | ||||||
chr14:96851816
|
T | C | 1 | a0001c0003t0001g0010 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.375-1015T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851816 | ||||||
chr14:96851876
|
A | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.375-955A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851876 | ||||||
chr14:96852421
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.375-410T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852421 | ||||||
chr14:96852809
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.375-22G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852809 | ||||||
chr14:96852817
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.375-14A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852817 | ||||||
chr14:96852823
|
G | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0216 | 2 | HG02683.hp1 HG02698.hp1 |
splice_region_variant&intron_variant | LOW | c.375-8G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852823 | ||||||
chr14:96852992
|
AG | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+55delG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 96852992 | |||||
chr14:96853174
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.576+8T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853174 | ||||||
chr14:96853303
|
T | C | 1 | a0001c0003t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.576+137T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853303 | ||||||
chr14:96853649
|
A | AT | 13 | a0001c0002t0001g0017a0001c0002t0001g0040a0001c0002t0001g0086others(10): Show | 14 | HG00733.hp1 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.576+493dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 96853649 | |||||
chr14:96853756
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.576+590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853756 | ||||||
chr14:96854020
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.576+854C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854020 | ||||||
chr14:96854062
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.576+896G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854062 | ||||||
chr14:96854086
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.576+920T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854086 | ||||||
chr14:96854184
|
T | C | 1 | a0001c0003t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.576+1018T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854184 | ||||||
chr14:96854208
|
A | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0217 | 3 | HG01192.hp1 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.577-1016A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854208 | ||||||
chr14:96854249
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.577-975A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854249 | ||||||
chr14:96854278
|
T | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-946T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854278 | ||||||
chr14:96854364
|
T | C | 11 | a0001c0003t0001g0002a0001c0003t0001g0013a0001c0003t0001g0014others(8): Show | 15 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.577-860T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854364 | ||||||
chr14:96854796
|
A | G | 5 | a0001c0003t0001g0001a0001c0003t0001g0042a0001c0003t0001g0045others(2): Show | 7 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-428A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854796 | ||||||
chr14:96854801
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.577-423C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854801 | ||||||
chr14:96854923
|
C | T | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.577-301C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854923 | ||||||
chr14:96854953
|
TATAAC | T | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.577-267_577-263del others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 96854953 | |||||
chr14:96855037
|
A | T | 2 | a0001c0003t0001g0001a0001c0003t0001g0045 | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-187A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96855037 | ||||||
chr14:96855431
|
G | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+75G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855431 | ||||||
chr14:96855432
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+76C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855432 | ||||||
chr14:96855499
|
G | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+143G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855499 | ||||||
chr14:96855799
|
G | A | 25 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0142others(22): Show | 26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-331G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855799 | ||||||
chr14:96855821
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.710-309A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855821 | ||||||
chr14:96856117
|
C | T | 1 | a0001c0002t0003g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.710-13C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96856117 | ||||||
chr14:96856749
|
A | T | 15 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(12): Show | 16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+163A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856749 | ||||||
chr14:96856773
|
C | T | 1 | a0001c0003t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.889+187C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856773 | ||||||
chr14:96856847
|
G | T | 55 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(52): Show | 67 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.889+261G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856847 | ||||||
chr14:96856892
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+306C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856892 | ||||||
chr14:96856893
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(3): Show | 7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+307G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856893 | ||||||
chr14:96856897
|
G | A | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.889+311G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856897 | ||||||
chr14:96856935
|
A | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0103 | 2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.889+349A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856935 | ||||||
chr14:96856969
|
G | GAAAA | 15 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(12): Show | 16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+389_889+392dup others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96856969 | |||||
chr14:96857193
|
T | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.889+607T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857193 | ||||||
chr14:96857337
|
CTTGGAAG others(22): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+752_889+780del others(29): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857337 | ||||||
chr14:96857338
|
T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 106 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.889+752T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857338 | ||||||
chr14:96857917
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+1331A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857917 | ||||||
chr14:96857952
|
A | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 74 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.889+1366A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857952 | ||||||
chr14:96857975
|
A | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0181 | 2 | HG00735.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.889+1389A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857975 | ||||||
chr14:96858011
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.889+1425C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858011 | ||||||
chr14:96858063
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0181 | 2 | HG00735.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.889+1477G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858063 | ||||||
chr14:96858240
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 78 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.889+1654C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858240 | ||||||
chr14:96858273
|
T | G | 1 | a0001c0003t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.889+1687T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858273 | ||||||
chr14:96858384
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+1798G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858384 | ||||||
chr14:96858674
|
T | C | 31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.890-1883T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858674 | ||||||
chr14:96858779
|
A | G | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.890-1778A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858779 | ||||||
chr14:96858922
|
C | A | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.890-1635C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858922 | ||||||
chr14:96859074
|
G | T | 1 | a0001c0002t0001g0108 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.890-1483G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859074 | ||||||
chr14:96859264
|
GTAGT | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0142others(22): Show | 26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.890-1291_890-1288d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96859264 | |||||
chr14:96859325
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.890-1232G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859325 | ||||||
chr14:96859379
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.890-1178G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859379 | ||||||
chr14:96859398
|
A | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.890-1159A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859398 | ||||||
chr14:96859586
|
T | G | 1 | a0001c0003t0001g0015 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.890-971T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859586 | ||||||
chr14:96859773
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.890-784C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859773 | ||||||
chr14:96859829
|
C | T | 28 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(25): Show | 32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.890-728C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859829 | ||||||
chr14:96859897
|
C | CAAGTCTG others(3): Show |
1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.890-659_890-650dup others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96859897 | |||||
chr14:96859931
|
A | G | 65 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(62): Show | 78 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.890-626A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859931 | ||||||
chr14:96860029
|
C | A | 68 | a0001c0002t0001g0008a0001c0002t0001g0018a0001c0002t0001g0019others(65): Show | 74 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.890-528C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860029 | ||||||
chr14:96860055
|
T | C | 7 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0173others(4): Show | 7 | HG00639.hp2 HG01257.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.890-502T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860055 | ||||||
chr14:96860391
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | NA18940.hp1 NA18952.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.890-166A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860391 | ||||||
chr14:96860486
|
A | G | 1 | a0001c0003t0001g0059 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.890-71A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860486 | ||||||
chr14:96860761
|
T | TTG | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+27_1068+28dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96860761 | |||||
chr14:96860798
|
AAG | A | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | HG02717.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1068+65_1068+66del others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96860798 | |||||
chr14:96860842
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1068+107A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860842 | ||||||
chr14:96860845
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+110G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860845 | ||||||
chr14:96860942
|
A | G | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1068+207A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860942 | ||||||
chr14:96861034
|
C | T | 3 | a0001c0003t0001g0059a0001c0003t0001g0068a0001c0003t0001g0073 | 3 | HG03831.hp2 HG03927.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1068+299C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861034 | ||||||
chr14:96861114
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1068+379G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861114 | ||||||
chr14:96861360
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+625A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861360 | ||||||
chr14:96861483
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1068+748A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861483 | ||||||
chr14:96861650
|
A | G | 2 | a0001c0003t0001g0001a0001c0003t0001g0045 | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068+915A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861650 | ||||||
chr14:96861707
|
C | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1068+972C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861707 | ||||||
chr14:96861752
|
T | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+1017T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861752 | ||||||
chr14:96861814
|
A | G | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(4): Show | 7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+1079A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861814 | ||||||
chr14:96861828
|
CTG | C | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+1095_1068+109 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96861828 | |||||
chr14:96862076
|
C | T | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1068+1341C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862076 | ||||||
chr14:96862145
|
A | G | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1410A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862145 | ||||||
chr14:96862152
|
A | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1417A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862152 | ||||||
chr14:96862328
|
A | G | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+1593A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862328 | ||||||
chr14:96862396
|
T | C | 2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1068+1661T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862396 | ||||||
chr14:96862510
|
G | GC | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1776dupC | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96862510 | |||||
chr14:96862511
|
C | CT | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 195 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1068+1789dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96862511 | |||||
chr14:96862796
|
C | G | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1068+2061C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862796 | ||||||
chr14:96862889
|
A | G | 10 | a0001c0003t0001g0012a0001c0003t0001g0043a0001c0003t0001g0052others(7): Show | 11 | HG00558.hp2 HG02080.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1068+2154A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862889 | ||||||
chr14:96862919
|
G | A | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+2184G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862919 | ||||||
chr14:96862979
|
T | A | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1068+2244T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862979 | ||||||
chr14:96863222
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1068+2487G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863222 | ||||||
chr14:96863336
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1068+2601A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863336 | ||||||
chr14:96863387
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1068+2652C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863387 | ||||||
chr14:96863635
|
T | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+2900T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863635 | ||||||
chr14:96863750
|
A | G | 1 | a0001c0003t0001g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1068+3015A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863750 | ||||||
chr14:96863812
|
A | T | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+3077A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863812 | ||||||
chr14:96863813
|
T | C | 127 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(124): Show | 146 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1068+3078T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863813 | ||||||
chr14:96863843
|
A | G | 1 | a0001c0002t0001g0026 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1068+3108A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863843 | ||||||
chr14:96863917
|
T | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1068+3182T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863917 | ||||||
chr14:96863933
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1068+3198C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863933 | ||||||
chr14:96863960
|
A | G | 1 | a0001c0003t0001g0062 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1068+3225A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863960 | ||||||
chr14:96864005
|
A | T | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+3270A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864005 | ||||||
chr14:96864061
|
A | G | 54 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(51): Show | 66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1068+3326A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864061 | ||||||
chr14:96864121
|
T | C | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(4): Show | 7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+3386T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864121 | ||||||
chr14:96864197
|
A | C | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+3462A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864197 | ||||||
chr14:96864261
|
AG | A | 30 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(27): Show | 34 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1068+3527delG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864261 | ||||||
chr14:96864379
|
T | G | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+3644T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864379 | ||||||
chr14:96864399
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1068+3664T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864399 | ||||||
chr14:96864438
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+3703C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864438 | ||||||
chr14:96864500
|
C | T | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1068+3765C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864500 | ||||||
chr14:96864509
|
T | C | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1068+3774T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864509 | ||||||
chr14:96864523
|
A | G | 1 | a0001c0003t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1068+3788A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864523 | ||||||
chr14:96864780
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1068+4045A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864780 | ||||||
chr14:96864792
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1068+4057G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864792 | ||||||
chr14:96864921
|
T | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1068+4186T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864921 | ||||||
chr14:96864921
|
T | TA | 59 | a0001c0002t0001g0017a0001c0002t0001g0087a0001c0003t0001g0001others(56): Show | 72 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1068+4198dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96864921 | |||||
chr14:96865046
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0226 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1068+4311A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865046 | ||||||
chr14:96865160
|
G | GA | 16 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0001t0001g0204others(13): Show | 17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+4427dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96865160 | |||||
chr14:96865281
|
T | C | 16 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0001t0001g0204others(13): Show | 17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+4546T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865281 | ||||||
chr14:96865328
|
G | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1068+4593G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865328 | ||||||
chr14:96865570
|
T | C | 4 | a0001c0002t0001g0017a0001c0002t0001g0087a0001c0003t0001g0009others(1): Show | 6 | HG00642.hp2 HG02572.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+4835T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865570 | ||||||
chr14:96865624
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0232 | 2 | NA18966.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1068+4889T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865624 | ||||||
chr14:96865683
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1068+4948C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865683 | ||||||
chr14:96865742
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1068+5007A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865742 | ||||||
chr14:96865760
|
T | TA | 42 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(39): Show | 46 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1068+5025_1068+502 others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865760 | ||||||
chr14:96865761
|
G | A | 88 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0019others(85): Show | 103 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1068+5026G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865761 | ||||||
chr14:96865761
|
G | GT | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(4): Show | 7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+5038dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96865761 | |||||
chr14:96865761
|
G | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(40): Show | 47 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1068+5026G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865761 | ||||||
chr14:96866061
|
A | T | 56 | a0001c0002t0001g0017a0001c0002t0001g0087a0001c0003t0001g0001others(53): Show | 69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1068+5326A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866061 | ||||||
chr14:96866140
|
T | C | 12 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(9): Show | 13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1068+5405T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866140 | ||||||
chr14:96866337
|
G | A | 6 | a0001c0002t0001g0018a0001c0002t0001g0096a0001c0002t0001g0097others(3): Show | 7 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068+5602G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866337 | ||||||
chr14:96866361
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+5626C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866361 | ||||||
chr14:96866434
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1068+5699A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866434 | ||||||
chr14:96866535
|
A | G | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1068+5800A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866535 | ||||||
chr14:96866559
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1068+5824G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866559 | ||||||
chr14:96866657
|
C | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1068+5922C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866657 | ||||||
chr14:96867020
|
A | C | 143 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0001t0001g0204others(140): Show | 162 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(159): Show |
intron_variant | MODIFIER | c.1068+6285A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867020 | ||||||
chr14:96867123
|
A | T | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+6388A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867123 | ||||||
chr14:96867225
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1068+6490A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867225 | ||||||
chr14:96867456
|
A | AGT | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 71 | HG00438.hp1 HG00639.hp2 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.1068+6756_1068+675 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
A | AGTGT | 8 | a0001c0001t0001g0039a0001c0001t0001g0165a0001c0001t0001g0167others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+6754_1068+675 others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGT | A | 8 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0002t0001g0006others(5): Show | 11 | HG00558.hp1 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1068+6756_1068+675 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGT | A | 75 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214others(72): Show | 87 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1068+6754_1068+675 others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGTGT | A | 27 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(24): Show | 32 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1068+6752_1068+675 others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0002t0001g0026a0001c0002t0001g0030a0001c0002t0001g0032others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+6750_1068+675 others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGTGTG others(3): Show |
A | 16 | a0001c0002t0001g0017a0001c0002t0001g0083a0001c0002t0001g0084others(13): Show | 17 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+6748_1068+675 others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGTGTG others(5): Show |
A | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG02602.hp1 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068+6746_1068+675 others(16): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867456
|
AGTGTGTG others(9): Show |
A | 3 | a0001c0003t0001g0081a0001c0003t0001g0093a0001c0003t0001g0094 | 3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1068+6742_1068+675 others(20): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | |||||
chr14:96867646
|
C | T | 2 | a0001c0002t0001g0237a0001c0002t0003g0240 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1068+6911C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867646 | ||||||
chr14:96867739
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1068+7004G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867739 | ||||||
chr14:96867865
|
A | G | 1 | a0001c0002t0001g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1068+7130A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867865 | ||||||
chr14:96867892
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1068+7157T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867892 | ||||||
chr14:96867973
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1068+7238G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867973 | ||||||
chr14:96868026
|
G | C | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+7291G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868026 | ||||||
chr14:96868107
|
A | G | 53 | a0001c0003t0001g0001a0001c0003t0001g0002a0001c0003t0001g0009others(50): Show | 65 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1068+7372A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868107 | ||||||
chr14:96868402
|
A | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-7628A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868402 | ||||||
chr14:96868405
|
A | G | 138 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(135): Show | 157 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.1069-7625A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868405 | ||||||
chr14:96868470
|
A | C | 2 | a0001c0002t0001g0083a0001c0002t0001g0085 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1069-7560A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868470 | ||||||
chr14:96868499
|
A | C | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-7531A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868499 | ||||||
chr14:96868779
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 79 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1069-7251G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868779 | ||||||
chr14:96868801
|
C | CT | 6 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0183others(3): Show | 6 | HG00738.hp2 HG02738.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-7211dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96868801 | |||||
chr14:96868801
|
CT | C | 115 | a0001c0002t0001g0006a0001c0002t0001g0018a0001c0002t0001g0019others(112): Show | 134 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(131): Show |
intron_variant | MODIFIER | c.1069-7211delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96868801 | |||||
chr14:96868808
|
T | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1069-7222T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868808 | ||||||
chr14:96868882
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1069-7148A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868882 | ||||||
chr14:96868889
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1069-7141G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868889 | ||||||
chr14:96868968
|
C | T | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 267 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.1069-7062C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868968 | ||||||
chr14:96869200
|
T | C | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1069-6830T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869200 | ||||||
chr14:96869222
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1069-6808C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869222 | ||||||
chr14:96869277
|
A | C | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(4): Show | 7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-6753A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869277 | ||||||
chr14:96869354
|
T | C | 3 | a0001c0003t0001g0076a0001c0003t0001g0077a0001c0003t0001g0078 | 3 | HG02080.hp2 NA18964.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1069-6676T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869354 | ||||||
chr14:96869631
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1069-6399G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869631 | ||||||
chr14:96869691
|
C | T | 132 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(129): Show | 151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.1069-6339C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869691 | ||||||
chr14:96869720
|
A | G | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-6310A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869720 | ||||||
chr14:96869720
|
A | T | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(4): Show | 7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-6310A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869720 | ||||||
chr14:96869880
|
A | G | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-6150A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869880 | ||||||
chr14:96869963
|
T | C | 2 | a0001c0003t0001g0093a0001c0003t0001g0094 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1069-6067T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869963 | ||||||
chr14:96869969
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1069-6061T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869969 | ||||||
chr14:96870122
|
G | A | 20 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(17): Show | 23 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.1069-5908G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870122 | ||||||
chr14:96870134
|
T | A | 2 | a0001c0003t0001g0010a0001c0003t0001g0050 | 3 | HG02717.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1069-5896T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870134 | ||||||
chr14:96870198
|
T | C | 132 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(129): Show | 151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.1069-5832T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870198 | ||||||
chr14:96870273
|
T | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-5757T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870273 | ||||||
chr14:96870415
|
G | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 81 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069-5615G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870415 | ||||||
chr14:96870554
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-5476C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870554 | ||||||
chr14:96870635
|
A | G | 1 | a0001c0002t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1069-5395A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870635 | ||||||
chr14:96871020
|
GT | G | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-5003delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96871020 | |||||
chr14:96871021
|
T | C | 1 | a0001c0003t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1069-5009T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871021 | ||||||
chr14:96871358
|
A | G | 6 | a0001c0003t0001g0013a0001c0003t0001g0064a0001c0003t0001g0065others(3): Show | 7 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-4672A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871358 | ||||||
chr14:96871387
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1069-4643A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871387 | ||||||
chr14:96871408
|
TA | T | 59 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(56): Show | 71 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1069-4621delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871408 | ||||||
chr14:96871659
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0169 | 2 | NA18946.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1069-4371T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871659 | ||||||
chr14:96871843
|
C | T | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-4187C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871843 | ||||||
chr14:96872003
|
G | C | 4 | a0001c0002t0001g0238a0001c0002t0001g0239a0001c0002t0001g0241others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-4027G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872003 | ||||||
chr14:96872053
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-3977C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872053 | ||||||
chr14:96872106
|
C | G | 1 | a0001c0002t0001g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1069-3924C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872106 | ||||||
chr14:96872149
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1069-3881T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872149 | ||||||
chr14:96872194
|
C | A | 1 | a0001c0002t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1069-3836C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872194 | ||||||
chr14:96872415
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0232 | 2 | NA18966.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1069-3615T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872415 | ||||||
chr14:96872440
|
G | A | 138 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(135): Show | 157 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.1069-3590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872440 | ||||||
chr14:96872479
|
A | G | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-3551A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872479 | ||||||
chr14:96872488
|
A | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 108 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1069-3542A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872488 | ||||||
chr14:96872587
|
C | T | 2 | a0001c0001t0001g0193a0001c0003t0001g0053 | 2 | HG00438.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1069-3443C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872587 | ||||||
chr14:96872588
|
G | A | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1069-3442G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872588 | ||||||
chr14:96872623
|
A | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0121a0001c0002t0001g0122 | 4 | HG03017.hp1 HG03239.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-3407A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872623 | ||||||
chr14:96872724
|
A | G | 10 | a0001c0003t0001g0012a0001c0003t0001g0043a0001c0003t0001g0052others(7): Show | 11 | HG00558.hp2 HG02080.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-3306A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872724 | ||||||
chr14:96872850
|
T | A | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-3180T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872850 | ||||||
chr14:96872851
|
T | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 267 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.1069-3179T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872851 | ||||||
chr14:96872995
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1069-3035A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872995 | ||||||
chr14:96873086
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1069-2944C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873086 | ||||||
chr14:96873199
|
T | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0206a0001c0001t0001g0209others(2): Show | 6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-2831T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873199 | ||||||
chr14:96873220
|
G | T | 5 | a0001c0002t0001g0086a0001c0002t0001g0088a0001c0002t0001g0089others(2): Show | 5 | HG02602.hp1 HG03098.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-2810G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873220 | ||||||
chr14:96873275
|
C | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-2755C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873275 | ||||||
chr14:96873681
|
T | C | 1 | a0001c0003t0001g0065 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1069-2349T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873681 | ||||||
chr14:96873691
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0226 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1069-2339G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873691 | ||||||
chr14:96874090
|
A | G | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-1940A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96874090 | ||||||
chr14:96874670
|
G | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-1360G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96874670 | ||||||
chr14:96875020
|
C | T | 3 | a0001c0003t0001g0060a0001c0003t0001g0067a0001c0003t0001g0069 | 3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1069-1010C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875020 | ||||||
chr14:96875100
|
T | G | 56 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(53): Show | 62 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1069-930T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875100 | ||||||
chr14:96875111
|
CTACAGAA others(2): Show |
C | 5 | a0001c0001t0001g0160a0001c0002t0001g0033a0001c0002t0001g0034others(2): Show | 5 | HG02630.hp1 HG03942.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-916_1069-908d others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96875111 | |||||
chr14:96875169
|
G | A | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1069-861G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875169 | ||||||
chr14:96875220
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1069-810G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875220 | ||||||
chr14:96875226
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1069-804T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875226 | ||||||
chr14:96875306
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-724C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875306 | ||||||
chr14:96875479
|
A | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1069-551A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875479 | ||||||
chr14:96875491
|
A | T | 140 | a0001c0001t0001g0160a0001c0002t0001g0008a0001c0002t0001g0017others(137): Show | 159 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069-539A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875491 | ||||||
chr14:96875541
|
T | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-489T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875541 | ||||||
chr14:96875546
|
T | G | 5 | a0001c0003t0001g0013a0001c0003t0001g0065a0001c0003t0001g0066others(2): Show | 6 | HG00639.hp1 HG00735.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-484T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875546 | ||||||
chr14:96875619
|
C | T | 1 | a0001c0003t0001g0052 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1069-411C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875619 | ||||||
chr14:96875743
|
T | G | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-287T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875743 | ||||||
chr14:96875793
|
TA | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 104 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1069-236delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875793 | ||||||
chr14:96875919
|
C | T | 3 | a0001c0003t0001g0060a0001c0003t0001g0067a0001c0003t0001g0069 | 3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1069-111C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875919 | ||||||
chr14:96876163
|
C | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+43C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876163 | ||||||
chr14:96876258
|
G | A | 5 | a0001c0002t0001g0086a0001c0002t0001g0088a0001c0002t0001g0089others(2): Show | 5 | HG02602.hp1 HG03098.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+138G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876258 | ||||||
chr14:96876390
|
G | A | 1 | a0001c0003t0001g0013 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1159+270G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876390 | ||||||
chr14:96876411
|
T | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+291T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876411 | ||||||
chr14:96876560
|
A | G | 2 | a0001c0002t0001g0121a0001c0002t0001g0122 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1159+440A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876560 | ||||||
chr14:96876694
|
G | A | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | HG02717.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1159+574G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876694 | ||||||
chr14:96876776
|
C | CA | 8 | a0001c0001t0001g0146a0001c0001t0001g0182a0001c0001t0001g0183others(5): Show | 8 | HG00558.hp1 HG02027.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159+671dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96876776 | |||||
chr14:96876776
|
CA | C | 131 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0001g0213others(128): Show | 150 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.1159+671delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96876776 | |||||
chr14:96876789
|
A | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00140.hp1 HG01175.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1159+669A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876789 | ||||||
chr14:96876794
|
C | A | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1159+674C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876794 | ||||||
chr14:96876986
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1159+866T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876986 | ||||||
chr14:96876986
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 117 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1159+866T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876986 | ||||||
chr14:96877067
|
C | CT | 7 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0176others(4): Show | 7 | HG00438.hp2 HG01515.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1159+960dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96877067 | |||||
chr14:96877634
|
T | A | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1159+1514T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877634 | ||||||
chr14:96877729
|
C | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1159+1609C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877729 | ||||||
chr14:96877807
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+1687A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877807 | ||||||
chr14:96878120
|
C | T | 31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1159+2000C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878120 | ||||||
chr14:96878493
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(1): Show | 4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+2373G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878493 | ||||||
chr14:96878675
|
G | T | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-2502G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878675 | ||||||
chr14:96878859
|
A | G | 1 | a0001c0003t0001g0062 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1160-2318A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878859 | ||||||
chr14:96878921
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1160-2256C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878921 | ||||||
chr14:96878932
|
T | C | 1 | a0001c0003t0001g0014 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1160-2245T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878932 | ||||||
chr14:96879236
|
T | TAAG | 136 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0001t0001g0204others(133): Show | 155 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.1160-1940_1160-193 others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96879236 | |||||
chr14:96879244
|
T | G | 11 | a0001c0002t0001g0019a0001c0002t0001g0109a0001c0002t0001g0110others(8): Show | 12 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160-1933T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879244 | ||||||
chr14:96879369
|
C | G | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1160-1808C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879369 | ||||||
chr14:96879469
|
G | A | 132 | a0001c0002t0001g0008a0001c0002t0001g0017a0001c0002t0001g0018others(129): Show | 151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.1160-1708G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879469 | ||||||
chr14:96879472
|
A | G | 16 | a0001c0002t0001g0019a0001c0002t0001g0104a0001c0002t0001g0105others(13): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1160-1705A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879472 | ||||||
chr14:96879493
|
T | C | 1 | a0001c0002t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1160-1684T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879493 | ||||||
chr14:96879535
|
G | A | 5 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-1642G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879535 | ||||||
chr14:96879651
|
G | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0194 | 4 | HG01891.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1526G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879651 | ||||||
chr14:96879758
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1160-1419A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879758 | ||||||
chr14:96879877
|
A | G | 2 | a0001c0003t0001g0001a0001c0003t0001g0045 | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1300A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879877 | ||||||
chr14:96879882
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1160-1295C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879882 | ||||||
chr14:96879926
|
C | CA | 21 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(18): Show | 22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1160-1240dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96879926 | |||||
chr14:96879957
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1160-1220A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879957 | ||||||
chr14:96880036
|
A | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160-1141A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880036 | ||||||
chr14:96880074
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0001g0103 | 2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1160-1103G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880074 | ||||||
chr14:96880101
|
G | A | 6 | a0001c0002t0001g0040a0001c0002t0001g0104a0001c0002t0001g0105others(3): Show | 6 | HG00733.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-1076G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880101 | ||||||
chr14:96880211
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1160-966A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880211 | ||||||
chr14:96880283
|
G | A | 7 | a0001c0002t0001g0017a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-894G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880283 | ||||||
chr14:96880296
|
A | G | 37 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(34): Show | 41 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1160-881A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880296 | ||||||
chr14:96880625
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1160-552C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880625 | ||||||
chr14:96880633
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1160-544A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880633 | ||||||
chr14:96880676
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1160-501G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880676 | ||||||
chr14:96880719
|
G | C | 25 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0142others(22): Show | 26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-458G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880719 | ||||||
chr14:96880720
|
T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-457T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880720 | ||||||
chr14:96880760
|
T | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0027others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160-417T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880760 | ||||||
chr14:96880769
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | NA18940.hp1 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-408A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880769 | ||||||
chr14:96880794
|
T | A | 59 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(56): Show | 71 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1160-383T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880794 |