geneid | 7444 |
---|---|
ensemblid | ENSG00000028116.18 |
hgncid | 12719 |
symbol | VRK2 |
name | VRK serine/threonine kinase 2 |
refseq_nuc | NM_006296.7 |
refseq_prot | NP_006287.2 |
ensembl_nuc | ENST00000340157.9 |
ensembl_prot | ENSP00000342381.4 |
mane_status | MANE Select |
chr | chr2 |
start | 58046806 |
end | 58159871 |
strand | + |
ver | v1.2 |
region | chr2:58046806-58159871 |
region5000 | chr2:58041806-58164871 |
regionname0 | VRK2_chr2_58046806_58159871 |
regionname5000 | VRK2_chr2_58041806_58164871 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 508 | 242 | 76 | 42 | 91 | 11 | 21 | 66 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0002 | 0/1 | 508 | 91 | 8 | 24 | 43 | 3 | 12 | 29 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0003 | 0/0 | 508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0004 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0005 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0006 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0007 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0008 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1527 | 221 | 58 | 39 | 91 | 11 | 21 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0002 | 0/1 | 1527 | 91 | 8 | 24 | 43 | 3 | 12 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0003 | 0/0 | 1527 | 18 | 18 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0004 | 0/0 | 1527 | 3 | 0 | 3 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0005 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0006 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0007 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0008 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0009 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
c0010 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 247 | 171 | 76 | 25 | 51 | 6 | 13 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
t0002 | 1/1 | 247 | 157 | 8 | 38 | 83 | 6 | 20 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
t0003 | 0/0 | 247 | 7 | 1 | 3 | 0 | 2 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
t0004 | 0/0 | 247 | 3 | 3 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
t0005 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
t0006 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1527 | 221 | 58 | 39 | 91 | 11 | 21 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0003 | 0/0 | 1527 | 18 | 18 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0004 | 0/0 | 1527 | 3 | 0 | 3 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0002c0002 | 0/1 | 1527 | 91 | 8 | 24 | 43 | 3 | 12 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0003c0005 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0004c0010 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0005c0007 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0006c0008 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0007c0009 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0008c0006 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1773 | 144 | 55 | 21 | 51 | 6 | 11 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0001t0002 | 1/0 | 1773 | 69 | 2 | 15 | 39 | 3 | 9 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0001t0003 | 0/0 | 1773 | 7 | 1 | 3 | 0 | 2 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0001t0006 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0003t0001 | 0/0 | 1773 | 15 | 15 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0003t0004 | 0/0 | 1773 | 3 | 3 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0001c0004t0001 | 0/0 | 1773 | 3 | 0 | 3 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0002c0002t0001 | 0/0 | 1773 | 5 | 2 | 1 | 0 | 0 | 2 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0002c0002t0002 | 0/1 | 1773 | 85 | 6 | 23 | 42 | 3 | 10 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0002c0002t0005 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0003c0005t0001 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0004c0010t0001 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0005c0007t0002 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0006c0008t0002 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0007c0009t0001 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
a0008c0006t0002 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | copy fasta | chr2 | 58041806 | 58164871 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0003t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0002c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0003c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0003c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0004c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0005c0007t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0006c0008t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0007c0009t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
a0008c0006t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0101 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0332 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0333 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0246 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0066 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0275 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0131 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0133 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02132 | hp2 | a0005 | c0007 | t0002 | g0221 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0132 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0009 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0292 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02683 | hp2 | a0008 | c0006 | t0002 | g0169 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0276 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02886 | hp2 | a0004 | c0010 | t0001 | g0151 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0012 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0011 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0114 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0286 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03579 | hp1 | a0007 | c0009 | t0001 | g0122 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0285 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | CHB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0271 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18998 | hp2 | a0006 | c0008 | t0002 | g0235 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0261 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19084 | hp1 | a0002 | c0002 | t0005 | g0104 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0273 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ASW | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0036 | EUR | TSI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | GIH | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | GIH | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02109 | hp2 | a0003 | c0005 | t0001 | g0115 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0088 | REF | REF | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0190 | REF | REF | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:58046866
|
C | T | 1 | a0001 | 7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
splice_region_variant | LOW | c.-8C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/13 | chr2 | 58046866 | ||||||
chr2:58048935
|
T | C | 1 | a0008 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.104T>C | p.Ile35Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/13 | 172/1773 | 104/1527 | 35/508 | chr2 | 58048935 | ||
chr2:58084100
|
A | G | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.148A>G | p.Asn50Asp | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/13 | 216/1773 | 148/1527 | 50/508 | chr2 | 58084100 | ||
chr2:58088400
|
A | C | 1 | a0007 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.404A>C | p.Asn135Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/13 | 472/1773 | 404/1527 | 135/508 | chr2 | 58088400 | ||
chr2:58089679
|
A | G | 2 | a0002a0006 | 92 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
missense_variant | MODERATE | c.499A>G | p.Ile167Val | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/13 | 567/1773 | 499/1527 | 167/508 | chr2 | 58089679 | ||
chr2:58139770
|
G | C | 1 | a0006 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.961G>C | p.Gly321Arg | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/13 | 1029/1773 | 961/1527 | 321/508 | chr2 | 58139770 | ||
chr2:58146446
|
T | C | 1 | a0005 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1154T>C | p.Ile385Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/13 | 1222/1773 | 1154/1527 | 385/508 | chr2 | 58146446 | ||
chr2:58159653
|
T | G | 1 | a0003 | 2 | HG02109.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.1487T>G | p.Val496Gly | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1555/1773 | 1487/1527 | 496/508 | chr2 | 58159653 | ||
chr2:58159670
|
T | C | 1 | a0003 | 2 | HG02109.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.1504T>C | p.Phe502Leu | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1572/1773 | 1504/1527 | 502/508 | chr2 | 58159670 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:58123205
|
T | C | 1 | a0001c0003 | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.648T>C | p.Phe216Phe | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/13 | 716/1773 | 648/1527 | 216/508 | chr2 | 58123205 | ||
chr2:58159432
|
T | C | 1 | a0001c0004 | 3 | HG01993.hp2 HG02004.hp2 HG02293.hp1 |
synonymous_variant | LOW | c.1266T>C | p.Tyr422Tyr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1334/1773 | 1266/1527 | 422/508 | chr2 | 58159432 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:58159750
|
T | C | 1 | a0001c0003t0004 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*57T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 57 | chr2 | 58159750 | |||||
chr2:58159797
|
T | C | 1 | a0002c0002t0005 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 104 | chr2 | 58159797 | |||||
chr2:58159808
|
A | AAGAGAAC others(4): Show |
1 | a0001c0001t0006 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116_*126dupAGAGAA others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 127 | INFO_REALIGN_3_PRIME | chr2 | 58159808 | ||||
chr2:58159865
|
C | T | 8 | a0001c0001t0001a0001c0003t0001a0001c0003t0004others(5): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 172 | chr2 | 58159865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:58046916
|
T | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+48T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58046916 | ||||||
chr2:58046924
|
C | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+56C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58046924 | ||||||
chr2:58047105
|
C | T | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6+237C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047105 | ||||||
chr2:58047191
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-6+323G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047191 | ||||||
chr2:58047219
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+351G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047219 | ||||||
chr2:58047361
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-6+493T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047361 | ||||||
chr2:58047496
|
C | T | 1 | a0001c0003t0001g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-6+628C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047496 | ||||||
chr2:58047531
|
G | T | 1 | a0002c0002t0002g0333 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-6+663G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047531 | ||||||
chr2:58047621
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+753G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047621 | ||||||
chr2:58047634
|
G | T | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-6+766G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047634 | ||||||
chr2:58047749
|
C | CAGG | 83 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0262others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-6+886_-6+888dupGG others(1): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 58047749 | |||||
chr2:58048047
|
A | T | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-780A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048047 | ||||||
chr2:58048168
|
A | C | 1 | a0001c0001t0001g0331 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5-659A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048168 | ||||||
chr2:58048210
|
T | G | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-5-617T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048210 | ||||||
chr2:58048367
|
C | T | 2 | a0002c0002t0001g0256a0002c0002t0002g0257 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-5-460C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048367 | ||||||
chr2:58048387
|
A | G | 11 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(8): Show | 11 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-440A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048387 | ||||||
chr2:58048531
|
G | A | 240 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-5-296G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048531 | ||||||
chr2:58048555
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-5-272T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048555 | ||||||
chr2:58048563
|
C | T | 2 | a0001c0003t0004g0011a0001c0003t0004g0012 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5-264C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048563 | ||||||
chr2:58048648
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5-179A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048648 | ||||||
chr2:58048775
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-5-52T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048775 | ||||||
chr2:58048980
|
C | G | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG01167.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+13C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58048980 | ||||||
chr2:58049029
|
A | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+62A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049029 | ||||||
chr2:58049074
|
A | G | 7 | a0002c0002t0002g0154a0002c0002t0002g0155a0002c0002t0002g0156others(4): Show | 7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+107A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049074 | ||||||
chr2:58049145
|
C | A | 105 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 106 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.136+178C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049145 | ||||||
chr2:58049884
|
T | TTGAA | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+934_136+937dup others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58049884 | |||||
chr2:58049896
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(38): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+929A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049896 | ||||||
chr2:58050049
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136+1082A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050049 | ||||||
chr2:58050130
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136+1163A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050130 | ||||||
chr2:58050139
|
G | T | 1 | a0001c0001t0001g0311 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136+1172G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050139 | ||||||
chr2:58050291
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136+1324T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050291 | ||||||
chr2:58050448
|
C | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+1481C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050448 | ||||||
chr2:58050456
|
C | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(21): Show | 24 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+1489C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050456 | ||||||
chr2:58050555
|
A | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1588A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050555 | ||||||
chr2:58050558
|
A | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+1591A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050558 | ||||||
chr2:58050708
|
G | A | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 12 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+1741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050708 | ||||||
chr2:58050762
|
T | C | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.136+1795T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050762 | ||||||
chr2:58050777
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.136+1810A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050777 | ||||||
chr2:58050788
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+1821C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050788 | ||||||
chr2:58050809
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.136+1842A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050809 | ||||||
chr2:58050861
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+1894T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050861 | ||||||
chr2:58050913
|
C | T | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1946C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050913 | ||||||
chr2:58050935
|
C | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+1968C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050935 | ||||||
chr2:58050975
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+2008T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050975 | ||||||
chr2:58051033
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+2066C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051033 | ||||||
chr2:58051160
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+2193A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051160 | ||||||
chr2:58051197
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.136+2230T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051197 | ||||||
chr2:58051336
|
G | A | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.136+2369G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051336 | ||||||
chr2:58051475
|
A | G | 24 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.136+2508A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051475 | ||||||
chr2:58051489
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+2522C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051489 | ||||||
chr2:58051546
|
A | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(38): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+2579A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051546 | ||||||
chr2:58051742
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.136+2775G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051742 | ||||||
chr2:58051782
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.136+2815G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051782 | ||||||
chr2:58051959
|
A | T | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+2992A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051959 | ||||||
chr2:58052015
|
G | T | 6 | a0001c0003t0001g0270a0001c0003t0001g0271a0001c0003t0001g0272others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+3048G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052015 | ||||||
chr2:58052151
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+3184C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052151 | ||||||
chr2:58052209
|
A | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.136+3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052209 | ||||||
chr2:58052313
|
A | G | 7 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+3346A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052313 | ||||||
chr2:58052446
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(42): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.136+3479C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052446 | ||||||
chr2:58052481
|
G | A | 1 | a0001c0003t0001g0259 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+3514G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052481 | ||||||
chr2:58052600
|
C | CA | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(23): Show | 27 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.136+3652dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58052600 | |||||
chr2:58052600
|
CA | C | 14 | a0001c0001t0001g0149a0001c0001t0001g0239a0001c0001t0001g0267others(11): Show | 14 | HG01243.hp2 HG01975.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+3652delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58052600 | |||||
chr2:58052920
|
C | A | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+3953C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052920 | ||||||
chr2:58053032
|
C | G | 1 | a0001c0001t0001g0308 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.136+4065C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053032 | ||||||
chr2:58053149
|
C | A | 1 | a0001c0003t0001g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+4182C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053149 | ||||||
chr2:58053317
|
A | G | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+4350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053317 | ||||||
chr2:58053663
|
A | C | 24 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+4696A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053663 | ||||||
chr2:58053708
|
A | G | 1 | a0002c0002t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136+4741A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053708 | ||||||
chr2:58053831
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+4864A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053831 | ||||||
chr2:58053912
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+4945T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053912 | ||||||
chr2:58053930
|
C | A | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+4963C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053930 | ||||||
chr2:58053949
|
T | C | 1 | a0001c0003t0001g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136+4982T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053949 | ||||||
chr2:58054007
|
G | A | 1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.136+5040G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054007 | ||||||
chr2:58054390
|
G | GT | 24 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+5435dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58054390 | |||||
chr2:58054431
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+5464T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054431 | ||||||
chr2:58054630
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.136+5663A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054630 | ||||||
chr2:58054777
|
A | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0315others(19): Show | 22 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.136+5810A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054777 | ||||||
chr2:58055270
|
G | A | 6 | a0001c0003t0001g0270a0001c0003t0001g0271a0001c0003t0001g0272others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+6303G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055270 | ||||||
chr2:58055384
|
C | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+6417C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055384 | ||||||
chr2:58055799
|
A | G | 2 | a0001c0003t0001g0010a0001c0003t0001g0013 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.136+6832A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055799 | ||||||
chr2:58055985
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.136+7018T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055985 | ||||||
chr2:58056032
|
GAA | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(36): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7066_136+7067d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056032 | ||||||
chr2:58056035
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(36): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7068C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056035 | ||||||
chr2:58056096
|
C | G | 4 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+7129C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056096 | ||||||
chr2:58056112
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.136+7145C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056112 | ||||||
chr2:58056401
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG01891.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.136+7434G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056401 | ||||||
chr2:58056465
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.136+7498T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056465 | ||||||
chr2:58056470
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.136+7503C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056470 | ||||||
chr2:58056563
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136+7596G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056563 | ||||||
chr2:58056600
|
C | G | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136+7633C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056600 | ||||||
chr2:58056611
|
A | ACT | 253 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.136+7646_136+7647d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58056611 | |||||
chr2:58056619
|
C | A | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136+7652C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056619 | ||||||
chr2:58056744
|
G | A | 2 | a0002c0002t0002g0026a0002c0002t0002g0027 | 2 | HG02738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136+7777G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056744 | ||||||
chr2:58056745
|
C | T | 1 | a0002c0002t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.136+7778C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056745 | ||||||
chr2:58056948
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136+7981A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056948 | ||||||
chr2:58056976
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.136+8009C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056976 | ||||||
chr2:58057035
|
G | A | 1 | a0001c0003t0001g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+8068G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057035 | ||||||
chr2:58057063
|
T | C | 1 | a0002c0002t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+8096T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057063 | ||||||
chr2:58057081
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+8114C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057081 | ||||||
chr2:58057113
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136+8146G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057113 | ||||||
chr2:58057411
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136+8444T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057411 | ||||||
chr2:58057414
|
T | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0290 | 3 | HG00323.hp2 HG00597.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.136+8447T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057414 | ||||||
chr2:58057503
|
CTCTT | C | 138 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(135): Show | 139 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.136+8540_136+8543d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58057503 | |||||
chr2:58057505
|
CTT | C | 6 | a0001c0001t0001g0102a0001c0001t0002g0176a0002c0002t0002g0103others(3): Show | 6 | HG00408.hp1 HG00423.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+8540_136+8541d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58057505 | |||||
chr2:58057533
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+8566G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057533 | ||||||
chr2:58057539
|
A | T | 1 | a0002c0002t0002g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136+8572A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057539 | ||||||
chr2:58057616
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0278others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+8649T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057616 | ||||||
chr2:58057765
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136+8798A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057765 | ||||||
chr2:58057873
|
C | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.136+8906C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057873 | ||||||
chr2:58058400
|
A | G | 1 | a0008c0006t0002g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136+9433A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058400 | ||||||
chr2:58058520
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+9553G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058520 | ||||||
chr2:58058599
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+9632T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058599 | ||||||
chr2:58058653
|
G | A | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+9686G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058653 | ||||||
chr2:58058732
|
C | G | 1 | a0002c0002t0002g0100 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.136+9765C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058732 | ||||||
chr2:58059192
|
A | G | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136+10225A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059192 | ||||||
chr2:58059258
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+10291A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059258 | ||||||
chr2:58059313
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136+10346G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059313 | ||||||
chr2:58059315
|
C | G | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+10348C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059315 | ||||||
chr2:58059566
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+10599C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059566 | ||||||
chr2:58059709
|
G | A | 1 | a0001c0003t0001g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+10742G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059709 | ||||||
chr2:58059778
|
ATAGT | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+10814_136+1081 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58059778 | |||||
chr2:58059836
|
A | G | 1 | a0002c0002t0002g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.136+10869A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059836 | ||||||
chr2:58060132
|
C | A | 1 | a0001c0001t0002g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.136+11165C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060132 | ||||||
chr2:58060221
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.136+11254G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060221 | ||||||
chr2:58060339
|
A | G | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.136+11372A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060339 | ||||||
chr2:58060364
|
G | T | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.136+11397G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060364 | ||||||
chr2:58060373
|
T | G | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+11406T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060373 | ||||||
chr2:58060495
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136+11528A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060495 | ||||||
chr2:58060543
|
T | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | NA18943.hp2 NA18947.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+11576T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060543 | ||||||
chr2:58060605
|
G | A | 1 | a0002c0002t0002g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.136+11638G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060605 | ||||||
chr2:58060822
|
C | T | 19 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.136+11855C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060822 | ||||||
chr2:58060887
|
A | G | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.136+11920A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060887 | ||||||
chr2:58061021
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136+12054A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061021 | ||||||
chr2:58061317
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136+12350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061317 | ||||||
chr2:58061418
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.136+12451G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061418 | ||||||
chr2:58061428
|
A | G | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+12461A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061428 | ||||||
chr2:58061441
|
A | T | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+12474A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061441 | ||||||
chr2:58061550
|
C | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+12583C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061550 | ||||||
chr2:58061553
|
A | G | 1 | a0002c0002t0002g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.136+12586A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061553 | ||||||
chr2:58061952
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+12985A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061952 | ||||||
chr2:58062191
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.136+13224A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062191 | ||||||
chr2:58062262
|
G | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+13295G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062262 | ||||||
chr2:58062506
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.136+13539C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062506 | ||||||
chr2:58062673
|
A | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+13706A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062673 | ||||||
chr2:58062855
|
G | A | 11 | a0001c0001t0002g0014a0001c0003t0001g0264a0001c0003t0001g0266others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+13888G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062855 | ||||||
chr2:58062862
|
A | G | 2 | a0001c0003t0001g0259a0001c0003t0001g0261 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+13895A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062862 | ||||||
chr2:58062910
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+13943C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062910 | ||||||
chr2:58062916
|
T | C | 23 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.136+13949T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062916 | ||||||
chr2:58062981
|
G | A | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14014G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062981 | ||||||
chr2:58063039
|
C | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+14072C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063039 | ||||||
chr2:58063086
|
A | G | 1 | a0006c0008t0002g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136+14119A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063086 | ||||||
chr2:58063132
|
G | C | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+14165G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063132 | ||||||
chr2:58063241
|
G | GT | 14 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | HG00738.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.136+14290dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58063241 | |||||
chr2:58063241
|
GT | G | 49 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(46): Show | 49 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.136+14290delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58063241 | |||||
chr2:58063248
|
T | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+14281T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063248 | ||||||
chr2:58063267
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.136+14300G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063267 | ||||||
chr2:58063306
|
G | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+14339G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063306 | ||||||
chr2:58063413
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.136+14446T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063413 | ||||||
chr2:58063421
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+14454G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063421 | ||||||
chr2:58063474
|
A | C | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14507A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063474 | ||||||
chr2:58063479
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136+14512A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063479 | ||||||
chr2:58063506
|
A | G | 7 | a0002c0002t0002g0154a0002c0002t0002g0155a0002c0002t0002g0156others(4): Show | 7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+14539A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063506 | ||||||
chr2:58063514
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.136+14547T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063514 | ||||||
chr2:58063569
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+14602A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063569 | ||||||
chr2:58063679
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.136+14712T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063679 | ||||||
chr2:58063774
|
A | G | 19 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.136+14807A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063774 | ||||||
chr2:58064397
|
A | G | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+15430A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064397 | ||||||
chr2:58064493
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136+15526G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064493 | ||||||
chr2:58064524
|
G | C | 1 | a0002c0002t0002g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136+15557G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064524 | ||||||
chr2:58064544
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+15577C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064544 | ||||||
chr2:58064875
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.136+15908A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064875 | ||||||
chr2:58065294
|
CT | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+16328delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065294 | ||||||
chr2:58065589
|
C | T | 4 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+16622C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065589 | ||||||
chr2:58065705
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.136+16738T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065705 | ||||||
chr2:58065728
|
A | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+16761A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065728 | ||||||
chr2:58065732
|
A | G | 1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.136+16765A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065732 | ||||||
chr2:58065827
|
G | A | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+16860G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065827 | ||||||
chr2:58065896
|
T | G | 6 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0034others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+16929T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065896 | ||||||
chr2:58066051
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+17084A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066051 | ||||||
chr2:58066165
|
C | G | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+17198C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066165 | ||||||
chr2:58066592
|
G | C | 1 | a0002c0002t0002g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.137-17497G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066592 | ||||||
chr2:58066792
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-17297G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066792 | ||||||
chr2:58066988
|
G | A | 9 | a0001c0001t0002g0014a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-17101G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066988 | ||||||
chr2:58067321
|
T | C | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-16768T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067321 | ||||||
chr2:58067401
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.137-16688C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067401 | ||||||
chr2:58067549
|
T | G | 4 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-16540T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067549 | ||||||
chr2:58067782
|
A | G | 23 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.137-16307A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067782 | ||||||
chr2:58067844
|
A | G | 1 | a0002c0002t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.137-16245A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067844 | ||||||
chr2:58067888
|
C | A | 1 | a0001c0001t0002g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137-16201C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067888 | ||||||
chr2:58067938
|
G | GT | 24 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.137-16142dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58067938 | |||||
chr2:58067982
|
T | G | 1 | a0002c0002t0002g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-16107T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067982 | ||||||
chr2:58067989
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-16100G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067989 | ||||||
chr2:58068193
|
G | A | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.137-15896G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068193 | ||||||
chr2:58068437
|
C | G | 2 | a0001c0001t0001g0121a0007c0009t0001g0122 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.137-15652C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068437 | ||||||
chr2:58068487
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-15602A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068487 | ||||||
chr2:58068630
|
T | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-15459T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068630 | ||||||
chr2:58068811
|
GA | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0099others(58): Show | 62 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.137-15260delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58068811 | |||||
chr2:58068811
|
GAA | G | 187 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(184): Show | 188 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.137-15261_137-1526 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58068811 | |||||
chr2:58068824
|
A | C | 39 | a0001c0001t0001g0025a0001c0001t0001g0123a0001c0001t0001g0124others(36): Show | 39 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.137-15265A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068824 | ||||||
chr2:58068830
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.137-15259C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068830 | ||||||
chr2:58068839
|
G | A | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.137-15250G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068839 | ||||||
chr2:58068844
|
T | C | 1 | a0002c0002t0002g0044 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.137-15245T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068844 | ||||||
chr2:58068949
|
A | G | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-15140A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068949 | ||||||
chr2:58069191
|
A | C | 19 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.137-14898A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069191 | ||||||
chr2:58069193
|
T | A | 1 | a0002c0002t0002g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-14896T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069193 | ||||||
chr2:58069362
|
C | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(59): Show | 62 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.137-14727C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069362 | ||||||
chr2:58069458
|
T | C | 2 | a0001c0003t0001g0271a0001c0003t0001g0272 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-14631T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069458 | ||||||
chr2:58069643
|
T | A | 1 | a0001c0003t0001g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137-14446T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069643 | ||||||
chr2:58069667
|
T | G | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-14422T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069667 | ||||||
chr2:58069755
|
A | G | 253 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.137-14334A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069755 | ||||||
chr2:58070093
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-13996C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070093 | ||||||
chr2:58070180
|
C | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-13909C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070180 | ||||||
chr2:58070211
|
T | A | 1 | a0002c0002t0002g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.137-13878T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070211 | ||||||
chr2:58070283
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.137-13806C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070283 | ||||||
chr2:58070344
|
C | T | 1 | a0001c0001t0002g0005 | 2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.137-13745C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070344 | ||||||
chr2:58070378
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.137-13711G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070378 | ||||||
chr2:58070468
|
C | T | 1 | a0002c0002t0002g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.137-13621C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070468 | ||||||
chr2:58070529
|
G | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.137-13560G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070529 | ||||||
chr2:58070618
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | NA18955.hp2 NA18992.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.137-13471T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070618 | ||||||
chr2:58070774
|
T | G | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0290 | 3 | HG00323.hp2 HG00597.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.137-13315T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070774 | ||||||
chr2:58071192
|
A | G | 1 | a0002c0002t0001g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137-12897A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071192 | ||||||
chr2:58071425
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-12664G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071425 | ||||||
chr2:58071433
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.137-12656A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071433 | ||||||
chr2:58071594
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.137-12495C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071594 | ||||||
chr2:58071673
|
C | G | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-12416C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071673 | ||||||
chr2:58071753
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.137-12336G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071753 | ||||||
chr2:58071856
|
A | G | 20 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(17): Show | 20 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-12233A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071856 | ||||||
chr2:58071944
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.137-12145A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071944 | ||||||
chr2:58072069
|
G | T | 4 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0036others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-12020G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072069 | ||||||
chr2:58072095
|
A | G | 1 | a0005c0007t0002g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.137-11994A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072095 | ||||||
chr2:58072191
|
A | G | 249 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.137-11898A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072191 | ||||||
chr2:58072225
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.137-11864G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072225 | ||||||
chr2:58072328
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-11761A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072328 | ||||||
chr2:58072489
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.137-11600G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072489 | ||||||
chr2:58072608
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137-11481C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072608 | ||||||
chr2:58072622
|
G | T | 1 | a0001c0001t0001g0305 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.137-11467G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072622 | ||||||
chr2:58072760
|
A | G | 1 | a0002c0002t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.137-11329A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072760 | ||||||
chr2:58072958
|
C | T | 64 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(61): Show | 64 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.137-11131C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072958 | ||||||
chr2:58073295
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.137-10794G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073295 | ||||||
chr2:58073349
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-10740C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073349 | ||||||
chr2:58073636
|
T | TTA | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-10437_137-1043 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073636 | |||||
chr2:58073648
|
A | ATATATT | 7 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0002g0215others(4): Show | 7 | HG01433.hp2 HG04199.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-10411_137-1040 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | |||||
chr2:58073648
|
ATATATT | A | 231 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.137-10411_137-1040 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | |||||
chr2:58073648
|
ATATATTT others(5): Show |
A | 1 | a0002c0002t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.137-10417_137-1040 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | |||||
chr2:58073648
|
ATATATTT others(11): Show |
A | 2 | a0001c0003t0001g0271a0001c0003t0001g0272 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-10423_137-1040 others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | |||||
chr2:58073779
|
C | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(60): Show | 64 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.137-10310C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073779 | ||||||
chr2:58073880
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(18): Show | 22 | HG01928.hp2 HG01934.hp2 HG02886.hp1 others(19): Show |
intron_variant | MODIFIER | c.137-10209A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073880 | ||||||
chr2:58074025
|
T | C | 1 | a0005c0007t0002g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.137-10064T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074025 | ||||||
chr2:58074202
|
T | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-9887T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074202 | ||||||
chr2:58074239
|
C | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.137-9850C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074239 | ||||||
chr2:58074372
|
A | G | 62 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(59): Show | 62 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.137-9717A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074372 | ||||||
chr2:58074413
|
G | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-9676G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074413 | ||||||
chr2:58074460
|
G | C | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-9629G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074460 | ||||||
chr2:58074503
|
C | T | 3 | a0001c0001t0001g0304a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG01975.hp1 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.137-9586C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074503 | ||||||
chr2:58074715
|
C | T | 5 | a0002c0002t0002g0080a0002c0002t0002g0081a0002c0002t0002g0097others(2): Show | 5 | NA18943.hp1 NA18951.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-9374C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074715 | ||||||
chr2:58074790
|
A | T | 1 | a0001c0001t0002g0290 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.137-9299A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074790 | ||||||
chr2:58074825
|
G | T | 1 | a0002c0002t0002g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.137-9264G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074825 | ||||||
chr2:58074848
|
C | A | 1 | a0001c0003t0001g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-9241C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074848 | ||||||
chr2:58074974
|
T | C | 2 | a0001c0001t0002g0185a0001c0001t0002g0186 | 2 | HG02523.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.137-9115T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074974 | ||||||
chr2:58075050
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-9039A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075050 | ||||||
chr2:58075182
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-8907A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075182 | ||||||
chr2:58075219
|
C | T | 23 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.137-8870C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075219 | ||||||
chr2:58075258
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-8831T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075258 | ||||||
chr2:58075374
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-8715G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075374 | ||||||
chr2:58075446
|
C | A | 1 | a0002c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.137-8643C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075446 | ||||||
chr2:58075478
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-8611G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075478 | ||||||
chr2:58075727
|
G | A | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8362G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075727 | ||||||
chr2:58075863
|
A | ACTT | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8226_137-8225i others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075863 | ||||||
chr2:58075865
|
A | T | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8224A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075865 | ||||||
chr2:58075866
|
A | AGAGTACT others(25): Show |
25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8223_137-8222i others(34): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075866 | ||||||
chr2:58075956
|
G | C | 22 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.137-8133G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075956 | ||||||
chr2:58076106
|
C | CT | 7 | a0001c0001t0002g0174a0001c0001t0002g0213a0001c0001t0002g0214others(4): Show | 7 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7965dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58076106 | |||||
chr2:58076106
|
CT | C | 132 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(129): Show | 133 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(130): Show |
intron_variant | MODIFIER | c.137-7965delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58076106 | |||||
chr2:58076309
|
C | A | 11 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-7780C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076309 | ||||||
chr2:58076378
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-7711A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076378 | ||||||
chr2:58076487
|
A | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-7602A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076487 | ||||||
chr2:58076494
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-7595T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076494 | ||||||
chr2:58076606
|
T | A | 1 | a0002c0002t0002g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7483T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076606 | ||||||
chr2:58076607
|
T | G | 1 | a0002c0002t0002g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7482T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076607 | ||||||
chr2:58076608
|
T | G | 1 | a0002c0002t0002g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7481T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076608 | ||||||
chr2:58076699
|
A | G | 1 | a0002c0002t0002g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.137-7390A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076699 | ||||||
chr2:58076758
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.137-7331C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076758 | ||||||
chr2:58076762
|
C | A | 7 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(4): Show | 7 | HG01993.hp2 HG02004.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7327C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076762 | ||||||
chr2:58076877
|
A | T | 13 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-7212A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076877 | ||||||
chr2:58076916
|
C | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-7173C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076916 | ||||||
chr2:58076963
|
T | C | 1 | a0002c0002t0002g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7126T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076963 | ||||||
chr2:58077135
|
A | G | 4 | a0001c0001t0001g0150a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-6954A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077135 | ||||||
chr2:58077260
|
A | G | 1 | a0002c0002t0002g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.137-6829A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077260 | ||||||
chr2:58077283
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137-6806T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077283 | ||||||
chr2:58077313
|
C | T | 10 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(7): Show | 10 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-6776C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077313 | ||||||
chr2:58077519
|
AT | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-6560delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58077519 | |||||
chr2:58077532
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.137-6557C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077532 | ||||||
chr2:58077660
|
T | G | 1 | a0002c0002t0002g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137-6429T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077660 | ||||||
chr2:58077743
|
G | A | 157 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.137-6346G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077743 | ||||||
chr2:58077908
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-6181A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077908 | ||||||
chr2:58078140
|
T | C | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | NA18970.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.137-5949T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078140 | ||||||
chr2:58078330
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-5759A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078330 | ||||||
chr2:58078389
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-5700T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078389 | ||||||
chr2:58078610
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-5479A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078610 | ||||||
chr2:58078616
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.137-5473G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078616 | ||||||
chr2:58078761
|
A | G | 1 | a0002c0002t0002g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137-5328A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078761 | ||||||
chr2:58078801
|
G | A | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-5288G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078801 | ||||||
chr2:58078846
|
T | C | 4 | a0001c0001t0002g0174a0001c0001t0002g0213a0001c0001t0002g0214others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5243T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078846 | ||||||
chr2:58078876
|
G | A | 9 | a0002c0002t0002g0049a0002c0002t0002g0227a0002c0002t0002g0229others(6): Show | 9 | HG01069.hp1 HG02027.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-5213G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078876 | ||||||
chr2:58078925
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.137-5164C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078925 | ||||||
chr2:58079593
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.137-4496A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079593 | ||||||
chr2:58079676
|
G | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.137-4413G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079676 | ||||||
chr2:58079902
|
A | G | 318 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(315): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.137-4187A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079902 | ||||||
chr2:58080213
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137-3876A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080213 | ||||||
chr2:58080331
|
G | T | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-3758G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080331 | ||||||
chr2:58080458
|
C | T | 5 | a0001c0001t0002g0177a0001c0001t0002g0187a0001c0001t0002g0211others(2): Show | 5 | HG02027.hp2 HG02074.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-3631C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080458 | ||||||
chr2:58080520
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137-3569A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080520 | ||||||
chr2:58080544
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-3545A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080544 | ||||||
chr2:58080648
|
G | C | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.137-3441G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080648 | ||||||
chr2:58080834
|
A | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-3255A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080834 | ||||||
chr2:58080868
|
C | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-3221C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080868 | ||||||
chr2:58080964
|
G | T | 1 | a0001c0001t0002g0210 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137-3125G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080964 | ||||||
chr2:58081024
|
C | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0262a0001c0001t0001g0313others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.137-3065C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081024 | ||||||
chr2:58081126
|
G | T | 26 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(23): Show | 26 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-2963G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081126 | ||||||
chr2:58081217
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.137-2872A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081217 | ||||||
chr2:58081321
|
C | A | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.137-2768C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081321 | ||||||
chr2:58081323
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0107 | 3 | HG00735.hp1 HG01261.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.137-2766G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081323 | ||||||
chr2:58081365
|
T | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-2724T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081365 | ||||||
chr2:58081386
|
A | G | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-2703A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081386 | ||||||
chr2:58081518
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-2571T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081518 | ||||||
chr2:58081561
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-2528T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081561 | ||||||
chr2:58081597
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137-2492T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081597 | ||||||
chr2:58081857
|
C | CGT | 95 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.137-2191_137-2190d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
C | CGTGT | 26 | a0001c0001t0001g0029a0001c0001t0001g0091a0001c0001t0001g0117others(23): Show | 27 | HG00438.hp1 HG00741.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.137-2193_137-2190d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
C | CGTGTGT | 6 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0239others(3): Show | 7 | HG01515.hp1 NA18945.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-2195_137-2190d others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0238a0001c0003t0001g0271a0001c0003t0001g0272 | 3 | HG02922.hp1 NA18906.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.137-2197_137-2190d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-2199_137-2190d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
CGT | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.137-2191_137-2190d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
CGTGT | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0165a0001c0001t0001g0166others(1): Show | 4 | HG01167.hp1 HG02040.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-2193_137-2190d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
CGTGTGT | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0123a0001c0001t0001g0124others(25): Show | 28 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.137-2195_137-2190d others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
CGTGTGTG others(1): Show |
C | 17 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0113others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.137-2197_137-2190d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081857
|
CGTGTGTG others(3): Show |
C | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-2199_137-2190d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | |||||
chr2:58081931
|
G | C | 1 | a0001c0001t0002g0236 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.137-2158G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081931 | ||||||
chr2:58082239
|
T | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(64): Show | 67 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.137-1850T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082239 | ||||||
chr2:58082288
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.137-1801G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082288 | ||||||
chr2:58082395
|
T | A | 1 | a0002c0002t0002g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.137-1694T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082395 | ||||||
chr2:58082472
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.137-1617G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082472 | ||||||
chr2:58082595
|
G | T | 151 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.137-1494G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082595 | ||||||
chr2:58082596
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-1493A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082596 | ||||||
chr2:58082617
|
T | TAA | 15 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-1472_137-1471i others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082617 | ||||||
chr2:58082732
|
A | G | 1 | a0002c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137-1357A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082732 | ||||||
chr2:58082824
|
T | A | 12 | a0001c0001t0001g0059a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-1265T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082824 | ||||||
chr2:58082896
|
T | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-1193T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082896 | ||||||
chr2:58082927
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137-1162T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082927 | ||||||
chr2:58082981
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.137-1108G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082981 | ||||||
chr2:58083124
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-965A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083124 | ||||||
chr2:58083144
|
C | T | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-945C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083144 | ||||||
chr2:58083438
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-651A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083438 | ||||||
chr2:58083559
|
G | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(42): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.137-530G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083559 | ||||||
chr2:58083659
|
A | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-430A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083659 | ||||||
chr2:58083747
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.137-342T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083747 | ||||||
chr2:58084152
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.186+14A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084152 | ||||||
chr2:58084489
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.186+351A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084489 | ||||||
chr2:58084549
|
T | C | 261 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.187-332T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084549 | ||||||
chr2:58084615
|
G | A | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-266G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084615 | ||||||
chr2:58084730
|
T | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-151T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084730 | ||||||
chr2:58084858
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187-23A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084858 | ||||||
chr2:58085150
|
A | G | 2 | a0001c0001t0002g0208a0001c0001t0002g0220 | 2 | HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.256+200A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085150 | ||||||
chr2:58085237
|
A | T | 1 | a0001c0003t0001g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.256+287A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085237 | ||||||
chr2:58085298
|
A | T | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.256+348A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085298 | ||||||
chr2:58085388
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.256+438A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085388 | ||||||
chr2:58085676
|
T | G | 1 | a0002c0002t0002g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.257-663T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085676 | ||||||
chr2:58085687
|
A | G | 2 | a0002c0002t0002g0076a0002c0002t0002g0077 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.257-652A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085687 | ||||||
chr2:58085930
|
C | CT | 66 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.257-393dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | |||||
chr2:58085930
|
CT | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(10): Show | 13 | HG00408.hp1 HG00558.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.257-393delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | |||||
chr2:58085930
|
CTTTTTTT others(1): Show |
C | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.257-400_257-393del others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | |||||
chr2:58085982
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0099 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.257-357A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085982 | ||||||
chr2:58086052
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.257-287A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086052 | ||||||
chr2:58086196
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.257-143T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086196 | ||||||
chr2:58086211
|
GA | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.257-120delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58086211 | |||||
chr2:58086217
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.257-122A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086217 | ||||||
chr2:58086237
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.257-102C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086237 | ||||||
chr2:58086239
|
A | G | 1 | a0002c0002t0002g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.257-100A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086239 | ||||||
chr2:58086467
|
A | G | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.344+41A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58086467 | ||||||
chr2:58086998
|
T | G | 1 | a0002c0002t0002g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.344+572T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58086998 | ||||||
chr2:58087007
|
A | G | 7 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+581A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087007 | ||||||
chr2:58087118
|
G | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(89): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.344+692G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087118 | ||||||
chr2:58087174
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.344+748T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087174 | ||||||
chr2:58087487
|
C | T | 3 | a0002c0002t0002g0058a0002c0002t0002g0090a0002c0002t0002g0100 | 3 | HG01496.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345-854C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087487 | ||||||
chr2:58087501
|
A | G | 4 | a0001c0001t0002g0174a0001c0001t0002g0213a0001c0001t0002g0214others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-840A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087501 | ||||||
chr2:58087502
|
A | G | 5 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231others(2): Show | 5 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-839A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087502 | ||||||
chr2:58087677
|
T | C | 1 | a0002c0002t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.345-664T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087677 | ||||||
chr2:58087699
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.345-642A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087699 | ||||||
chr2:58087718
|
G | C | 2 | a0002c0002t0002g0285a0002c0002t0002g0286 | 2 | HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.345-623G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087718 | ||||||
chr2:58087726
|
T | C | 11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-615T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087726 | ||||||
chr2:58087972
|
C | A | 1 | a0002c0002t0002g0234 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.345-369C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087972 | ||||||
chr2:58088123
|
T | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.345-218T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58088123 | ||||||
chr2:58088467
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+21A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088467 | ||||||
chr2:58088500
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+54T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088500 | ||||||
chr2:58088657
|
G | C | 1 | a0002c0002t0002g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.450+211G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088657 | ||||||
chr2:58088707
|
A | G | 2 | a0002c0002t0002g0233a0004c0010t0001g0151 | 2 | HG02027.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.450+261A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088707 | ||||||
chr2:58088867
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+421T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088867 | ||||||
chr2:58088946
|
A | G | 25 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(22): Show | 25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.450+500A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088946 | ||||||
chr2:58088985
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+539A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088985 | ||||||
chr2:58089052
|
A | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.451-579A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58089052 | ||||||
chr2:58089317
|
CTA | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-312_451-311del others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 58089317 | |||||
chr2:58089367
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.451-264A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58089367 | ||||||
chr2:58090073
|
A | G | 19 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090073 | ||||||
chr2:58090270
|
C | T | 1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+547C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090270 | ||||||
chr2:58090400
|
C | CA | 25 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0054others(22): Show | 25 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+698dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58090400 | |||||
chr2:58090486
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+763A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090486 | ||||||
chr2:58090669
|
G | A | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+946G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090669 | ||||||
chr2:58090786
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+1063C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090786 | ||||||
chr2:58090787
|
G | A | 3 | a0001c0001t0002g0014a0003c0005t0001g0114a0003c0005t0001g0115 | 3 | HG02109.hp2 HG02970.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.543+1064G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090787 | ||||||
chr2:58090896
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+1173A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090896 | ||||||
chr2:58091061
|
G | A | 1 | a0006c0008t0002g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.543+1338G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091061 | ||||||
chr2:58091122
|
T | G | 1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+1399T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091122 | ||||||
chr2:58091221
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543+1498A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091221 | ||||||
chr2:58091246
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.543+1523A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091246 | ||||||
chr2:58091263
|
A | C | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+1540A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091263 | ||||||
chr2:58091566
|
AAAATGTA others(4254): Show |
A | 1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.543+1846_543+6106d others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58091566 | |||||
chr2:58091688
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0330a0001c0001t0002g0213 | 3 | HG00735.hp2 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+1965C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091688 | ||||||
chr2:58091689
|
G | T | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.543+1966G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091689 | ||||||
chr2:58092321
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+2598T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092321 | ||||||
chr2:58092429
|
G | A | 2 | a0002c0002t0002g0154a0002c0002t0002g0158 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+2706G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092429 | ||||||
chr2:58092480
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+2757T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092480 | ||||||
chr2:58092545
|
A | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2822A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092545 | ||||||
chr2:58092629
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+2906T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092629 | ||||||
chr2:58092642
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+2919A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092642 | ||||||
chr2:58092729
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+3006A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092729 | ||||||
chr2:58093026
|
G | GTA | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+3309_543+3310d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58093026 | |||||
chr2:58093121
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.543+3398C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093121 | ||||||
chr2:58093321
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | NA18977.hp2 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.543+3598G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093321 | ||||||
chr2:58093380
|
A | G | 5 | a0001c0003t0001g0010a0001c0003t0001g0013a0001c0003t0004g0009others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093380 | ||||||
chr2:58093476
|
C | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0253 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.543+3753C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093476 | ||||||
chr2:58093544
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+3821T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093544 | ||||||
chr2:58093663
|
G | A | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+3940G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093663 | ||||||
chr2:58093670
|
T | G | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+3947T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093670 | ||||||
chr2:58093694
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.543+3971T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093694 | ||||||
chr2:58093723
|
T | A | 2 | a0002c0002t0002g0154a0002c0002t0002g0158 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+4000T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093723 | ||||||
chr2:58093993
|
C | T | 4 | a0001c0003t0001g0270a0001c0003t0001g0273a0001c0003t0001g0274others(1): Show | 4 | HG01884.hp2 HG02572.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+4270C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093993 | ||||||
chr2:58094012
|
C | G | 2 | a0001c0001t0002g0241a0001c0001t0002g0242 | 2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.543+4289C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094012 | ||||||
chr2:58094166
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+4443A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094166 | ||||||
chr2:58094370
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+4647A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094370 | ||||||
chr2:58094574
|
G | C | 2 | a0002c0002t0002g0063a0002c0002t0002g0110 | 2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.543+4851G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094574 | ||||||
chr2:58094898
|
T | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.543+5175T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094898 | ||||||
chr2:58094917
|
G | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+5194G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094917 | ||||||
chr2:58095022
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+5299G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095022 | ||||||
chr2:58095091
|
A | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.543+5368A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095091 | ||||||
chr2:58095092
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.543+5369G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095092 | ||||||
chr2:58095154
|
C | T | 1 | a0001c0003t0001g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+5431C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095154 | ||||||
chr2:58095166
|
T | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.543+5443T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095166 | ||||||
chr2:58095226
|
G | A | 1 | a0005c0007t0002g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.543+5503G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095226 | ||||||
chr2:58095293
|
C | CAAAAA | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+5585_543+5589d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58095293 | |||||
chr2:58095293
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0002g0014a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+5581_543+5589d others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58095293 | |||||
chr2:58095340
|
T | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+5617T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095340 | ||||||
chr2:58095457
|
A | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+5734A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095457 | ||||||
chr2:58095524
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0082 | 3 | HG01928.hp2 HG01934.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.543+5801T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095524 | ||||||
chr2:58095606
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543+5883A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095606 | ||||||
chr2:58095710
|
A | G | 1 | a0002c0002t0002g0075 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.543+5987A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095710 | ||||||
chr2:58095898
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.543+6175A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095898 | ||||||
chr2:58095983
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+6260T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095983 | ||||||
chr2:58095984
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+6261G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095984 | ||||||
chr2:58096053
|
A | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.543+6330A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096053 | ||||||
chr2:58096196
|
A | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+6473A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096196 | ||||||
chr2:58096236
|
T | C | 1 | a0002c0002t0002g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.543+6513T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096236 | ||||||
chr2:58096420
|
T | A | 1 | a0002c0002t0002g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.543+6697T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096420 | ||||||
chr2:58096591
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+6868A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096591 | ||||||
chr2:58096789
|
A | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+7066A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096789 | ||||||
chr2:58096824
|
A | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+7101A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096824 | ||||||
chr2:58097261
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+7538G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097261 | ||||||
chr2:58097279
|
TTCTC | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+7560_543+7563d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097279 | |||||
chr2:58097404
|
C | A | 3 | a0001c0003t0001g0270a0001c0003t0001g0273a0001c0003t0001g0275 | 3 | HG01884.hp2 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.543+7681C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097404 | ||||||
chr2:58097410
|
G | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(73): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.543+7687G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097410 | ||||||
chr2:58097467
|
A | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+7744A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097467 | ||||||
chr2:58097589
|
T | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+7866T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097589 | ||||||
chr2:58097645
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+7922A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097645 | ||||||
chr2:58097718
|
T | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+7995T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097718 | ||||||
chr2:58097827
|
CTA | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+8106_543+8107d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097827 | |||||
chr2:58097896
|
TA | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.543+8182delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097896 | |||||
chr2:58097958
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+8235T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097958 | ||||||
chr2:58097992
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+8269T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097992 | ||||||
chr2:58097997
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+8274T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097997 | ||||||
chr2:58098065
|
T | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+8342T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098065 | ||||||
chr2:58098159
|
G | A | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+8436G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098159 | ||||||
chr2:58098241
|
T | A | 1 | a0002c0002t0002g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.543+8518T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098241 | ||||||
chr2:58098510
|
T | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(18): Show | 21 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.543+8787T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098510 | ||||||
chr2:58098610
|
A | AGCC | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+8888_543+8890d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58098610 | |||||
chr2:58098665
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+8942T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098665 | ||||||
chr2:58099245
|
T | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+9522T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099245 | ||||||
chr2:58099279
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+9556G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099279 | ||||||
chr2:58099293
|
T | C | 2 | a0002c0002t0002g0078a0006c0008t0002g0235 | 2 | NA18986.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.543+9570T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099293 | ||||||
chr2:58099313
|
A | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+9590A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099313 | ||||||
chr2:58099343
|
A | G | 1 | a0001c0001t0002g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.543+9620A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099343 | ||||||
chr2:58099588
|
T | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+9865T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099588 | ||||||
chr2:58099609
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+9886G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099609 | ||||||
chr2:58099735
|
C | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+10012C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099735 | ||||||
chr2:58099750
|
T | A | 16 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.543+10027T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099750 | ||||||
chr2:58099751
|
T | G | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+10028T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099751 | ||||||
chr2:58099797
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.543+10074C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099797 | ||||||
chr2:58100102
|
A | G | 1 | a0002c0002t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.543+10379A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100102 | ||||||
chr2:58100235
|
G | C | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+10512G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100235 | ||||||
chr2:58100333
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+10610A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100333 | ||||||
chr2:58100335
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+10612A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100335 | ||||||
chr2:58100524
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+10801C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100524 | ||||||
chr2:58100554
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+10831T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100554 | ||||||
chr2:58100614
|
ATATTT | A | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+10895_543+1089 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58100614 | |||||
chr2:58100734
|
A | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.543+11011A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100734 | ||||||
chr2:58100847
|
A | C | 2 | a0001c0001t0002g0208a0001c0001t0002g0220 | 2 | HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.543+11124A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100847 | ||||||
chr2:58100983
|
T | G | 1 | a0001c0001t0001g0311 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.543+11260T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100983 | ||||||
chr2:58101051
|
TAG | T | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.543+11331_543+1133 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58101051 | |||||
chr2:58101108
|
A | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+11385A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101108 | ||||||
chr2:58101115
|
T | C | 4 | a0001c0001t0002g0187a0001c0001t0002g0211a0001c0001t0002g0212others(1): Show | 4 | HG02027.hp2 HG02074.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+11392T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101115 | ||||||
chr2:58101211
|
A | G | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+11488A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101211 | ||||||
chr2:58101317
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.543+11594T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101317 | ||||||
chr2:58101598
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.543+11875T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101598 | ||||||
chr2:58101746
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.543+12023G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101746 | ||||||
chr2:58101762
|
G | A | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+12039G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101762 | ||||||
chr2:58101855
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+12132T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101855 | ||||||
chr2:58101908
|
T | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+12185T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101908 | ||||||
chr2:58101950
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+12227A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101950 | ||||||
chr2:58101993
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.543+12270G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101993 | ||||||
chr2:58102118
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0278a0001c0001t0001g0279 | 4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+12395T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102118 | ||||||
chr2:58102320
|
T | A | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+12597T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102320 | ||||||
chr2:58102321
|
A | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+12598A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102321 | ||||||
chr2:58102337
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+12614A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102337 | ||||||
chr2:58102376
|
A | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+12653A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102376 | ||||||
chr2:58102406
|
A | C | 1 | a0001c0001t0002g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.543+12683A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102406 | ||||||
chr2:58102492
|
T | TA | 46 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(43): Show | 46 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+12784dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58102492 | |||||
chr2:58102570
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+12847A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102570 | ||||||
chr2:58102646
|
A | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+12923A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102646 | ||||||
chr2:58102782
|
C | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+13059C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102782 | ||||||
chr2:58102818
|
T | C | 11 | a0001c0001t0002g0174a0001c0001t0002g0213a0001c0001t0002g0214others(8): Show | 11 | HG00735.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+13095T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102818 | ||||||
chr2:58102866
|
T | C | 9 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | NA18943.hp2 NA18947.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+13143T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102866 | ||||||
chr2:58102979
|
G | A | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+13256G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102979 | ||||||
chr2:58103583
|
C | T | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+13860C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103583 | ||||||
chr2:58103614
|
C | T | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.543+13891C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103614 | ||||||
chr2:58103637
|
A | G | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+13914A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103637 | ||||||
chr2:58103947
|
C | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.543+14224C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103947 | ||||||
chr2:58103969
|
A | G | 2 | a0002c0002t0002g0080a0002c0002t0005g0104 | 2 | NA19012.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.543+14246A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103969 | ||||||
chr2:58104006
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.543+14283T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104006 | ||||||
chr2:58104076
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.543+14353A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104076 | ||||||
chr2:58104250
|
T | A | 1 | a0002c0002t0002g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.543+14527T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104250 | ||||||
chr2:58104382
|
A | G | 1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+14659A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104382 | ||||||
chr2:58104405
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.543+14682C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104405 | ||||||
chr2:58104458
|
TACAGTA | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+14738_543+1474 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58104458 | |||||
chr2:58104497
|
T | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+14774T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104497 | ||||||
chr2:58104576
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.543+14853A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104576 | ||||||
chr2:58104660
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.543+14937T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104660 | ||||||
chr2:58104767
|
A | G | 4 | a0001c0001t0002g0193a0001c0001t0002g0198a0001c0001t0002g0205others(1): Show | 4 | HG00408.hp2 HG02155.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+15044A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104767 | ||||||
chr2:58104909
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.543+15186A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104909 | ||||||
chr2:58105066
|
G | A | 1 | a0002c0002t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.543+15343G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105066 | ||||||
chr2:58105399
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+15676T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105399 | ||||||
chr2:58105622
|
A | C | 26 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(23): Show | 26 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.543+15899A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105622 | ||||||
chr2:58105726
|
G | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+16003G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105726 | ||||||
chr2:58105856
|
T | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+16133T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105856 | ||||||
chr2:58106037
|
T | G | 1 | a0001c0001t0002g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543+16314T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106037 | ||||||
chr2:58106092
|
C | T | 1 | a0001c0003t0001g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+16369C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106092 | ||||||
chr2:58106155
|
T | C | 1 | a0002c0002t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.543+16432T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106155 | ||||||
chr2:58106158
|
A | G | 1 | a0002c0002t0002g0234 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.543+16435A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106158 | ||||||
chr2:58106170
|
G | GT | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+16453dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58106170 | |||||
chr2:58106183
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.543+16460A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106183 | ||||||
chr2:58106320
|
C | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+16597C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106320 | ||||||
chr2:58106422
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-16679G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106422 | ||||||
chr2:58106578
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-16523A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106578 | ||||||
chr2:58106636
|
T | G | 1 | a0001c0001t0002g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-16465T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106636 | ||||||
chr2:58106692
|
T | C | 19 | a0001c0001t0001g0147a0001c0001t0001g0262a0001c0001t0001g0313others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-16409T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106692 | ||||||
chr2:58106751
|
CAG | C | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-16348_544-1634 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58106751 | |||||
chr2:58107095
|
T | TG | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-16005dupG | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58107095 | |||||
chr2:58107104
|
G | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-15997G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107104 | ||||||
chr2:58107113
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-15988T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107113 | ||||||
chr2:58107151
|
AT | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-15949delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107151 | ||||||
chr2:58107472
|
T | A | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15629T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107472 | ||||||
chr2:58107492
|
CTTCCTAG others(7): Show |
C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-15605_544-1559 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58107492 | |||||
chr2:58107516
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-15585C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107516 | ||||||
chr2:58107531
|
T | C | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15570T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107531 | ||||||
chr2:58107646
|
A | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-15455A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107646 | ||||||
chr2:58107664
|
A | C | 326 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(323): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.544-15437A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107664 | ||||||
chr2:58107664
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0002g0188 | 3 | HG01099.hp1 HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.544-15437A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107664 | ||||||
chr2:58107734
|
A | G | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15367A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107734 | ||||||
chr2:58107773
|
C | T | 19 | a0001c0001t0001g0147a0001c0001t0001g0262a0001c0001t0001g0313others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-15328C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107773 | ||||||
chr2:58107790
|
A | G | 332 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.544-15311A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107790 | ||||||
chr2:58107851
|
A | G | 3 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0220 | 3 | HG00558.hp1 HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.544-15250A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107851 | ||||||
chr2:58107900
|
C | G | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-15201C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107900 | ||||||
chr2:58107940
|
G | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-15161G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107940 | ||||||
chr2:58107946
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.544-15155G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107946 | ||||||
chr2:58108043
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.544-15058C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108043 | ||||||
chr2:58108051
|
C | G | 22 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-15050C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108051 | ||||||
chr2:58108084
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.544-15017A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108084 | ||||||
chr2:58108320
|
T | A | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-14781T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108320 | ||||||
chr2:58108422
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-14679C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108422 | ||||||
chr2:58108522
|
T | C | 17 | a0001c0001t0001g0147a0001c0001t0001g0262a0001c0001t0001g0315others(14): Show | 17 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.544-14579T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108522 | ||||||
chr2:58108546
|
T | C | 90 | a0002c0002t0001g0023a0002c0002t0001g0152a0002c0002t0001g0153others(87): Show | 91 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.544-14555T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108546 | ||||||
chr2:58108621
|
C | G | 25 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.544-14480C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108621 | ||||||
chr2:58108745
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-14356C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108745 | ||||||
chr2:58108940
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.544-14161A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108940 | ||||||
chr2:58108999
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.544-14102C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108999 | ||||||
chr2:58109082
|
TGCTTGGC others(17): Show |
T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-13994_544-1397 others(28): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58109082 | |||||
chr2:58109091
|
C | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-14010C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109091 | ||||||
chr2:58109149
|
G | T | 22 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-13952G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109149 | ||||||
chr2:58109226
|
T | C | 21 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-13875T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109226 | ||||||
chr2:58109393
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.544-13708T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109393 | ||||||
chr2:58109434
|
GA | G | 8 | a0001c0001t0001g0117a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-13654delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58109434 | |||||
chr2:58109579
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-13522A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109579 | ||||||
chr2:58109676
|
G | A | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-13425G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109676 | ||||||
chr2:58109875
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544-13226A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109875 | ||||||
chr2:58109967
|
G | C | 1 | a0002c0002t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.544-13134G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109967 | ||||||
chr2:58110012
|
A | G | 2 | a0001c0001t0002g0207a0001c0001t0006g0206 | 2 | HG02083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-13089A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110012 | ||||||
chr2:58110055
|
T | C | 1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.544-13046T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110055 | ||||||
chr2:58110192
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-12909T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110192 | ||||||
chr2:58110400
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12701C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110400 | ||||||
chr2:58110572
|
C | T | 1 | a0001c0003t0001g0260 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544-12529C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110572 | ||||||
chr2:58110860
|
A | T | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-12241A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110860 | ||||||
chr2:58110925
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-12176C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110925 | ||||||
chr2:58110951
|
A | G | 94 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(91): Show | 95 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.544-12150A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110951 | ||||||
chr2:58111012
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12089A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111012 | ||||||
chr2:58111035
|
G | A | 1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.544-12066G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111035 | ||||||
chr2:58111051
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12050A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111051 | ||||||
chr2:58111073
|
C | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-12028C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111073 | ||||||
chr2:58111110
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.544-11991G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111110 | ||||||
chr2:58111318
|
T | C | 167 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.544-11783T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111318 | ||||||
chr2:58111319
|
C | A | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.544-11782C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111319 | ||||||
chr2:58111381
|
A | C | 2 | a0001c0003t0001g0274a0001c0003t0001g0275 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.544-11720A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111381 | ||||||
chr2:58111402
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.544-11699G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111402 | ||||||
chr2:58111637
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.544-11464C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111637 | ||||||
chr2:58111662
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-11439A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111662 | ||||||
chr2:58111770
|
G | A | 7 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-11331G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111770 | ||||||
chr2:58111823
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-11278C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111823 | ||||||
chr2:58112087
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.544-11014G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112087 | ||||||
chr2:58112148
|
A | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-10953A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112148 | ||||||
chr2:58112442
|
A | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.544-10659A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112442 | ||||||
chr2:58112576
|
G | GA | 110 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(107): Show | 110 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.544-10513dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58112576 | |||||
chr2:58112576
|
G | GAAA | 11 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.544-10515_544-1051 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58112576 | |||||
chr2:58112584
|
A | AG | 54 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(51): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.544-10517_544-1051 others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112584 | ||||||
chr2:58113182
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0278a0001c0001t0001g0279 | 4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-9919G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113182 | ||||||
chr2:58113300
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9801G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113300 | ||||||
chr2:58113307
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.544-9794C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113307 | ||||||
chr2:58113312
|
C | CA | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0055others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-9771dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58113312 | |||||
chr2:58113312
|
CA | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0082a0001c0001t0001g0141others(19): Show | 22 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-9771delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58113312 | |||||
chr2:58113394
|
C | T | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-9707C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113394 | ||||||
chr2:58113424
|
A | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0287 | 2 | NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.544-9677A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113424 | ||||||
chr2:58113596
|
A | G | 9 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-9505A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113596 | ||||||
chr2:58113648
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9453G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113648 | ||||||
chr2:58113686
|
G | A | 23 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(20): Show | 23 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-9415G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113686 | ||||||
chr2:58113810
|
C | G | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-9291C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113810 | ||||||
chr2:58113833
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0330 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.544-9268G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113833 | ||||||
chr2:58113863
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.544-9238C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113863 | ||||||
chr2:58113890
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9211T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113890 | ||||||
chr2:58113922
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-9179C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113922 | ||||||
chr2:58113937
|
G | A | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-9164G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113937 | ||||||
chr2:58113974
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.544-9127T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113974 | ||||||
chr2:58114244
|
A | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.544-8857A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114244 | ||||||
chr2:58114272
|
T | C | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8829T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114272 | ||||||
chr2:58114284
|
G | T | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8817G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114284 | ||||||
chr2:58114292
|
A | C | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8809A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114292 | ||||||
chr2:58114308
|
C | T | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8793C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114308 | ||||||
chr2:58114318
|
T | C | 1 | a0002c0002t0002g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.544-8783T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114318 | ||||||
chr2:58114342
|
A | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8759A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114342 | ||||||
chr2:58114356
|
G | A | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8745G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114356 | ||||||
chr2:58114382
|
A | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-8719A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114382 | ||||||
chr2:58114562
|
C | G | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-8539C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114562 | ||||||
chr2:58114569
|
G | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.544-8532G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114569 | ||||||
chr2:58114615
|
T | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8486T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114615 | ||||||
chr2:58114664
|
C | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8437C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114664 | ||||||
chr2:58114672
|
C | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8429C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114672 | ||||||
chr2:58114673
|
A | G | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-8428A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114673 | ||||||
chr2:58114698
|
A | AACC | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8403_544-8402i others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114698 | ||||||
chr2:58114703
|
G | A | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-8398G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114703 | ||||||
chr2:58114892
|
C | G | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-8209C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114892 | ||||||
chr2:58115092
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-8009G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115092 | ||||||
chr2:58115327
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-7774A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115327 | ||||||
chr2:58115426
|
A | G | 11 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(8): Show | 11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7675A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115426 | ||||||
chr2:58115427
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(8): Show | 11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7674C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115427 | ||||||
chr2:58115444
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(8): Show | 11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7657G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115444 | ||||||
chr2:58115496
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-7605G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115496 | ||||||
chr2:58115513
|
G | A | 3 | a0002c0002t0002g0276a0002c0002t0002g0285a0002c0002t0002g0286 | 3 | HG02698.hp2 HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.544-7588G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115513 | ||||||
chr2:58115545
|
ATTTG | A | 89 | a0001c0001t0001g0296a0002c0002t0001g0023a0002c0002t0001g0256others(86): Show | 90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.544-7551_544-7548d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58115545 | |||||
chr2:58115697
|
C | G | 6 | a0001c0003t0001g0270a0001c0003t0001g0271a0001c0003t0001g0272others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-7404C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115697 | ||||||
chr2:58115739
|
GGATGAAA others(1): Show |
G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-7361_544-7354d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115739 | ||||||
chr2:58115767
|
C | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-7334C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115767 | ||||||
chr2:58115785
|
C | G | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.544-7316C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115785 | ||||||
chr2:58115972
|
C | T | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.544-7129C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115972 | ||||||
chr2:58116225
|
G | A | 1 | a0002c0002t0002g0087 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-6876G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116225 | ||||||
chr2:58116249
|
A | C | 22 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-6852A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116249 | ||||||
chr2:58116284
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-6817A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116284 | ||||||
chr2:58116320
|
C | G | 173 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.544-6781C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116320 | ||||||
chr2:58116336
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-6765C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116336 | ||||||
chr2:58116337
|
G | A | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6764G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116337 | ||||||
chr2:58116341
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6760A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116341 | ||||||
chr2:58116348
|
G | A | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6753G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116348 | ||||||
chr2:58116401
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544-6700G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116401 | ||||||
chr2:58116429
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544-6672A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116429 | ||||||
chr2:58116436
|
T | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-6665T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116436 | ||||||
chr2:58116438
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-6663A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116438 | ||||||
chr2:58116443
|
A | G | 5 | a0002c0002t0002g0042a0002c0002t0002g0075a0002c0002t0002g0086others(2): Show | 5 | NA18966.hp1 NA18975.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-6658A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116443 | ||||||
chr2:58116455
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-6646G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116455 | ||||||
chr2:58116596
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-6505C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116596 | ||||||
chr2:58116690
|
C | T | 1 | a0002c0002t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.544-6411C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116690 | ||||||
chr2:58116769
|
A | G | 2 | a0001c0003t0001g0270a0001c0003t0001g0273 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.544-6332A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116769 | ||||||
chr2:58116777
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.544-6324G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116777 | ||||||
chr2:58116794
|
C | T | 7 | a0002c0002t0002g0154a0002c0002t0002g0155a0002c0002t0002g0156others(4): Show | 7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-6307C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116794 | ||||||
chr2:58116795
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.544-6306G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116795 | ||||||
chr2:58116885
|
G | T | 1 | a0002c0002t0002g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.544-6216G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116885 | ||||||
chr2:58116941
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-6160C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116941 | ||||||
chr2:58116988
|
G | A | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-6113G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116988 | ||||||
chr2:58117054
|
G | A | 90 | a0002c0002t0001g0023a0002c0002t0001g0152a0002c0002t0001g0153others(87): Show | 91 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.544-6047G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117054 | ||||||
chr2:58117093
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.544-6008G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117093 | ||||||
chr2:58117181
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-5920G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117181 | ||||||
chr2:58117418
|
A | G | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-5683A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117418 | ||||||
chr2:58117511
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-5590G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117511 | ||||||
chr2:58117514
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-5587G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117514 | ||||||
chr2:58117657
|
C | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0171a0001c0001t0002g0178others(15): Show | 19 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-5444C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117657 | ||||||
chr2:58117711
|
G | A | 1 | a0002c0002t0002g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.544-5390G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117711 | ||||||
chr2:58117740
|
T | G | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.544-5361T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117740 | ||||||
chr2:58117748
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.544-5353A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117748 | ||||||
chr2:58117751
|
G | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-5350G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117751 | ||||||
chr2:58117773
|
C | T | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.544-5328C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117773 | ||||||
chr2:58117852
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.544-5249G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117852 | ||||||
chr2:58117946
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.544-5155G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117946 | ||||||
chr2:58118006
|
A | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-5095A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118006 | ||||||
chr2:58118090
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(8): Show | 11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-5011C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118090 | ||||||
chr2:58118122
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0004c0010t0001g0151 | 3 | HG02559.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-4979A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118122 | ||||||
chr2:58118258
|
A | T | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-4843A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118258 | ||||||
chr2:58118301
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.544-4800C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118301 | ||||||
chr2:58118315
|
C | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4786C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118315 | ||||||
chr2:58118337
|
T | C | 4 | a0001c0003t0001g0270a0001c0003t0001g0273a0001c0003t0001g0274others(1): Show | 4 | HG01884.hp2 HG02572.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-4764T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118337 | ||||||
chr2:58118360
|
G | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-4741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118360 | ||||||
chr2:58118381
|
C | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(47): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-4720C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118381 | ||||||
chr2:58118392
|
G | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-4709G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118392 | ||||||
chr2:58118397
|
T | C | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4704T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118397 | ||||||
chr2:58118473
|
T | A | 1 | a0001c0001t0002g0175 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.544-4628T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118473 | ||||||
chr2:58118553
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.544-4548G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118553 | ||||||
chr2:58118607
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.544-4494C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118607 | ||||||
chr2:58118679
|
TC | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-4420delC | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58118679 | |||||
chr2:58118682
|
G | A | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-4419G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118682 | ||||||
chr2:58118779
|
G | A | 3 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0002g0292 | 3 | HG01516.hp2 HG02258.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.544-4322G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118779 | ||||||
chr2:58118884
|
T | C | 25 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(22): Show | 25 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.544-4217T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118884 | ||||||
chr2:58118975
|
G | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | NA18977.hp2 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.544-4126G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118975 | ||||||
chr2:58119026
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-4075C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119026 | ||||||
chr2:58119099
|
C | T | 1 | a0002c0002t0002g0077 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-4002C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119099 | ||||||
chr2:58119234
|
A | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-3867A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119234 | ||||||
chr2:58119300
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-3801C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119300 | ||||||
chr2:58119309
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.544-3792C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119309 | ||||||
chr2:58119343
|
C | CA | 12 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0013others(9): Show | 12 | HG01168.hp2 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-3742dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119343 | |||||
chr2:58119343
|
CA | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0102others(25): Show | 28 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.544-3742delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119343 | |||||
chr2:58119376
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-3725C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119376 | ||||||
chr2:58119409
|
G | A | 8 | a0002c0002t0002g0227a0002c0002t0002g0229a0002c0002t0002g0230others(5): Show | 8 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-3692G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119409 | ||||||
chr2:58119426
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3675G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119426 | ||||||
chr2:58119476
|
C | CA | 101 | a0001c0001t0001g0085a0001c0001t0001g0134a0001c0001t0001g0143others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.544-3607dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119476 | |||||
chr2:58119476
|
C | CAA | 8 | a0002c0002t0001g0023a0002c0002t0002g0026a0002c0002t0002g0035others(5): Show | 8 | HG01168.hp2 HG01255.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-3608_544-3607d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119476 | |||||
chr2:58119583
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-3518G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119583 | ||||||
chr2:58119665
|
C | T | 1 | a0002c0002t0002g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.544-3436C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119665 | ||||||
chr2:58119830
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0239 | 2 | NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.544-3271A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119830 | ||||||
chr2:58119831
|
A | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-3270A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119831 | ||||||
chr2:58119952
|
A | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-3149A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119952 | ||||||
chr2:58120076
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.544-3025T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120076 | ||||||
chr2:58120179
|
CTTTTCTT others(6): Show |
C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-2917_544-2905d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120179 | |||||
chr2:58120179
|
CTTTTCTT others(7): Show |
C | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2917_544-2904d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120179 | |||||
chr2:58120184
|
C | CT | 6 | a0001c0001t0001g0030a0001c0001t0001g0107a0001c0001t0002g0176others(3): Show | 6 | HG00423.hp1 HG00558.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-2893dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTCTTT others(15): Show |
1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544-2914_544-2913i others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0328 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.544-2902_544-2893d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2903_544-2893d others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0281a0001c0001t0001g0300a0001c0001t0001g0301others(2): Show | 5 | HG03041.hp1 HG03540.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2904_544-2893d others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0282a0001c0001t0001g0324a0001c0001t0001g0325others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-2905_544-2893d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(7): Show |
9 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0180others(6): Show | 10 | HG02145.hp1 HG03453.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2906_544-2893d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0083others(8): Show | 11 | HG02738.hp1 HG03209.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2907_544-2893d others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(9): Show |
16 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0082others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.544-2908_544-2893d others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0059others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-2909_544-2893d others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(11): Show |
15 | a0001c0001t0001g0015a0001c0001t0001g0123a0001c0001t0001g0125others(12): Show | 15 | HG00280.hp1 HG01975.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.544-2910_544-2893d others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0295a0001c0004t0001g0131 | 2 | HG00438.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.544-2911_544-2893d others(21): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(13): Show |
2 | a0001c0004t0001g0132a0001c0004t0001g0133 | 2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.544-2912_544-2893d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0166a0001c0001t0001g0289others(1): Show | 4 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-2914_544-2893d others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.544-2916_544-2893d others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2893_544-2892i others(27): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.544-2893_544-2892i others(29): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-2893_544-2892i others(32): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
CT | C | 83 | a0001c0001t0002g0174a0001c0001t0002g0213a0001c0001t0002g0214others(80): Show | 84 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.544-2893delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120184
|
CTT | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-2894_544-2893d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | |||||
chr2:58120191
|
T | C | 1 | a0001c0001t0002g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-2910T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120191 | ||||||
chr2:58120301
|
C | T | 19 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0262others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-2800C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120301 | ||||||
chr2:58120420
|
A | T | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.544-2681A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120420 | ||||||
chr2:58120637
|
C | T | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2464C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120637 | ||||||
chr2:58120707
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.544-2394T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120707 | ||||||
chr2:58120794
|
T | C | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2307T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120794 | ||||||
chr2:58120810
|
C | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-2291C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120810 | ||||||
chr2:58121230
|
T | G | 1 | a0001c0001t0001g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.544-1871T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121230 | ||||||
chr2:58121340
|
G | A | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-1761G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121340 | ||||||
chr2:58121487
|
C | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-1614C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121487 | ||||||
chr2:58121548
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-1553A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121548 | ||||||
chr2:58121592
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-1509A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121592 | ||||||
chr2:58121888
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.544-1213T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121888 | ||||||
chr2:58122132
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-969T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122132 | ||||||
chr2:58122698
|
C | G | 1 | a0002c0002t0002g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544-403C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122698 | ||||||
chr2:58122766
|
C | T | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-335C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122766 | ||||||
chr2:58122767
|
T | G | 1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-334T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122767 | ||||||
chr2:58122769
|
C | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-332C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122769 | ||||||
chr2:58122772
|
A | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-329A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122772 | ||||||
chr2:58122782
|
A | G | 1 | a0002c0002t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.544-319A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122782 | ||||||
chr2:58122822
|
T | C | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-279T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122822 | ||||||
chr2:58122830
|
T | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-271T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122830 | ||||||
chr2:58122925
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.544-176G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122925 | ||||||
chr2:58123369
|
A | G | 324 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.676+136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123369 | ||||||
chr2:58123388
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+155A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123388 | ||||||
chr2:58123397
|
T | C | 26 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.676+164T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123397 | ||||||
chr2:58123436
|
G | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.676+203G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123436 | ||||||
chr2:58123533
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+300A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123533 | ||||||
chr2:58123771
|
C | G | 1 | a0001c0003t0001g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+538C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123771 | ||||||
chr2:58123853
|
GA | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+634delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58123853 | |||||
chr2:58123862
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+629A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123862 | ||||||
chr2:58123936
|
C | G | 1 | a0002c0002t0002g0074 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.676+703C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123936 | ||||||
chr2:58123955
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.676+722T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123955 | ||||||
chr2:58124308
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676+1075C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124308 | ||||||
chr2:58124552
|
C | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+1319C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124552 | ||||||
chr2:58124793
|
G | A | 1 | a0001c0003t0001g0007 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676+1560G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124793 | ||||||
chr2:58124796
|
A | G | 5 | a0001c0001t0002g0038a0001c0001t0002g0194a0001c0001t0002g0200others(2): Show | 5 | HG02071.hp1 HG02165.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+1563A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124796 | ||||||
chr2:58124914
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0183 | 2 | NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.676+1681T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124914 | ||||||
chr2:58124924
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.676+1691G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124924 | ||||||
chr2:58125049
|
A | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+1816A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125049 | ||||||
chr2:58125119
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.676+1886G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125119 | ||||||
chr2:58125316
|
A | G | 1 | a0001c0003t0001g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676+2083A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125316 | ||||||
chr2:58125456
|
T | A | 1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676+2223T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125456 | ||||||
chr2:58125551
|
T | G | 1 | a0002c0002t0002g0229 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.676+2318T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125551 | ||||||
chr2:58125613
|
G | GT | 11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+2384dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58125613 | |||||
chr2:58125741
|
T | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.676+2508T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125741 | ||||||
chr2:58125762
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.676+2529A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125762 | ||||||
chr2:58125890
|
A | G | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+2657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125890 | ||||||
chr2:58126121
|
T | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+2888T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126121 | ||||||
chr2:58126129
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676+2896A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126129 | ||||||
chr2:58126141
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.676+2908A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126141 | ||||||
chr2:58126259
|
A | G | 1 | a0001c0003t0001g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.676+3026A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126259 | ||||||
chr2:58126377
|
TTTCTATG others(13): Show |
T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+3146_676+3165d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58126377 | |||||
chr2:58126450
|
C | G | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3217C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126450 | ||||||
chr2:58126475
|
A | G | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126475 | ||||||
chr2:58126541
|
TGATG | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+3315_676+3318d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58126541 | |||||
chr2:58126543
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.676+3310A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126543 | ||||||
chr2:58126578
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+3345T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126578 | ||||||
chr2:58126602
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.676+3369A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126602 | ||||||
chr2:58126651
|
C | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+3418C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126651 | ||||||
chr2:58126665
|
A | G | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.676+3432A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126665 | ||||||
chr2:58126930
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+3697C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126930 | ||||||
chr2:58127150
|
T | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.676+3917T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127150 | ||||||
chr2:58127229
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.676+3996G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127229 | ||||||
chr2:58127249
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.676+4016T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127249 | ||||||
chr2:58127287
|
A | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.676+4054A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127287 | ||||||
chr2:58127298
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676+4065A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127298 | ||||||
chr2:58127417
|
C | T | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.676+4184C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127417 | ||||||
chr2:58127421
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+4188A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127421 | ||||||
chr2:58127799
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.677-4009C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127799 | ||||||
chr2:58127836
|
G | A | 88 | a0002c0002t0001g0023a0002c0002t0001g0256a0002c0002t0002g0001others(85): Show | 89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.677-3972G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127836 | ||||||
chr2:58127863
|
T | C | 8 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(5): Show | 8 | HG02735.hp2 HG02738.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-3945T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127863 | ||||||
chr2:58128077
|
T | G | 27 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(24): Show | 27 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-3731T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128077 | ||||||
chr2:58128144
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677-3664T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128144 | ||||||
chr2:58128144
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.677-3664T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128144 | ||||||
chr2:58128172
|
G | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-3636G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128172 | ||||||
chr2:58128441
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.677-3367C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128441 | ||||||
chr2:58128566
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.677-3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128566 | ||||||
chr2:58128751
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.677-3057C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128751 | ||||||
chr2:58128892
|
G | A | 5 | a0002c0002t0002g0080a0002c0002t0002g0081a0002c0002t0002g0097others(2): Show | 5 | NA18943.hp1 NA18951.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-2916G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128892 | ||||||
chr2:58129244
|
A | C | 1 | a0001c0001t0002g0175 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.677-2564A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129244 | ||||||
chr2:58129525
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-2283A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129525 | ||||||
chr2:58129526
|
T | A | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-2282T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129526 | ||||||
chr2:58129692
|
T | C | 12 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-2116T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129692 | ||||||
chr2:58129920
|
G | T | 13 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-1888G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129920 | ||||||
chr2:58130151
|
A | G | 1 | a0001c0003t0001g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-1657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130151 | ||||||
chr2:58130437
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.677-1371G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130437 | ||||||
chr2:58130471
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677-1337G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130471 | ||||||
chr2:58130710
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.677-1098T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130710 | ||||||
chr2:58131102
|
G | T | 1 | a0002c0002t0002g0257 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.677-706G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131102 | ||||||
chr2:58131361
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.677-447A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131361 | ||||||
chr2:58131368
|
G | A | 1 | a0003c0005t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-440G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131368 | ||||||
chr2:58131373
|
C | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-435C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131373 | ||||||
chr2:58131398
|
A | G | 1 | a0002c0002t0001g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.677-410A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131398 | ||||||
chr2:58131441
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-367G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131441 | ||||||
chr2:58131534
|
G | A | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.677-274G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131534 | ||||||
chr2:58131605
|
A | G | 1 | a0002c0002t0002g0232 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.677-203A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131605 | ||||||
chr2:58131675
|
C | G | 21 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.677-133C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131675 | ||||||
chr2:58131693
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-115C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131693 | ||||||
chr2:58131935
|
A | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.797+7A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58131935 | ||||||
chr2:58132211
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.797+283T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132211 | ||||||
chr2:58132276
|
C | T | 1 | a0002c0002t0002g0333 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.797+348C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132276 | ||||||
chr2:58132348
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.797+420A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132348 | ||||||
chr2:58132406
|
T | G | 1 | a0001c0003t0001g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.797+478T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132406 | ||||||
chr2:58132545
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.797+617A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132545 | ||||||
chr2:58132624
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0006g0206 | 3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.797+696A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132624 | ||||||
chr2:58132695
|
C | G | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.797+767C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132695 | ||||||
chr2:58132724
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.797+796G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132724 | ||||||
chr2:58132922
|
A | G | 7 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(4): Show | 7 | HG01993.hp2 HG02004.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.797+994A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132922 | ||||||
chr2:58132959
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.797+1031T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132959 | ||||||
chr2:58133131
|
T | C | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.797+1203T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133131 | ||||||
chr2:58133230
|
T | TTATC | 39 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(36): Show | 39 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.797+1305_797+1306i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58133230 | |||||
chr2:58133247
|
A | G | 19 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+1319A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133247 | ||||||
chr2:58133269
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.797+1341A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133269 | ||||||
chr2:58133474
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.797+1546G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133474 | ||||||
chr2:58133487
|
G | C | 5 | a0001c0001t0001g0117a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG02145.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.797+1559G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133487 | ||||||
chr2:58133510
|
T | C | 16 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.797+1582T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133510 | ||||||
chr2:58133835
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.798-1306A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133835 | ||||||
chr2:58133857
|
C | T | 1 | a0002c0002t0002g0077 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798-1284C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133857 | ||||||
chr2:58133976
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798-1165C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133976 | ||||||
chr2:58133999
|
G | A | 90 | a0002c0002t0001g0023a0002c0002t0001g0152a0002c0002t0001g0153others(87): Show | 91 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.798-1142G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133999 | ||||||
chr2:58134013
|
A | C | 1 | a0001c0001t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.798-1128A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134013 | ||||||
chr2:58134041
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.798-1100T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134041 | ||||||
chr2:58134088
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.798-1053A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134088 | ||||||
chr2:58134098
|
T | A | 2 | a0002c0002t0001g0256a0002c0002t0002g0257 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.798-1043T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134098 | ||||||
chr2:58134120
|
T | C | 37 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(34): Show | 37 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.798-1021T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134120 | ||||||
chr2:58134182
|
G | A | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-959G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134182 | ||||||
chr2:58134213
|
A | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-928A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134213 | ||||||
chr2:58134228
|
T | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-913T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134228 | ||||||
chr2:58134236
|
G | A | 18 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.798-905G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134236 | ||||||
chr2:58134291
|
C | G | 1 | a0002c0002t0002g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.798-850C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134291 | ||||||
chr2:58134349
|
C | T | 1 | a0002c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.798-792C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134349 | ||||||
chr2:58134378
|
G | A | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.798-763G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134378 | ||||||
chr2:58134385
|
G | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-756G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134385 | ||||||
chr2:58134410
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798-731G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134410 | ||||||
chr2:58134462
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.798-679T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134462 | ||||||
chr2:58134540
|
A | G | 1 | a0001c0001t0002g0216 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.798-601A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134540 | ||||||
chr2:58134617
|
C | CA | 78 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(75): Show | 79 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.798-504dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | |||||
chr2:58134617
|
C | CAA | 58 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0059others(55): Show | 58 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.798-505_798-504dup others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | |||||
chr2:58134617
|
C | CAAA | 6 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0125others(3): Show | 6 | HG01109.hp1 HG01952.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.798-506_798-504dup others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | |||||
chr2:58134617
|
CA | C | 6 | a0001c0001t0001g0096a0001c0001t0003g0248a0001c0001t0003g0249others(3): Show | 6 | HG01070.hp1 HG01256.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.798-504delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | |||||
chr2:58134634
|
A | T | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.798-507A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134634 | ||||||
chr2:58134768
|
G | T | 7 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.798-373G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134768 | ||||||
chr2:58134809
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.798-332T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134809 | ||||||
chr2:58134884
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-257T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134884 | ||||||
chr2:58135026
|
G | A | 88 | a0002c0002t0001g0023a0002c0002t0001g0256a0002c0002t0002g0001others(85): Show | 89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.798-115G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58135026 | ||||||
chr2:58135207
|
A | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.856+8A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135207 | ||||||
chr2:58135382
|
G | C | 11 | a0002c0002t0002g0061a0002c0002t0002g0064a0002c0002t0002g0067others(8): Show | 11 | HG00408.hp1 HG00558.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.856+183G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135382 | ||||||
chr2:58135408
|
A | G | 1 | a0002c0002t0002g0234 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.856+209A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135408 | ||||||
chr2:58135441
|
C | CT | 32 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0313others(29): Show | 33 | HG01099.hp1 HG01106.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.856+258dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58135441 | |||||
chr2:58135441
|
CT | C | 7 | a0001c0001t0001g0123a0001c0001t0001g0141a0001c0001t0001g0150others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+258delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58135441 | |||||
chr2:58135473
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856+274A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135473 | ||||||
chr2:58135508
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.856+309G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135508 | ||||||
chr2:58135682
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856+483T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135682 | ||||||
chr2:58135823
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+624C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135823 | ||||||
chr2:58135894
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.856+695C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135894 | ||||||
chr2:58136181
|
C | A | 1 | a0002c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.856+982C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136181 | ||||||
chr2:58136214
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.856+1015C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136214 | ||||||
chr2:58136277
|
GGA | G | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.856+1083_856+1084d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136277 | |||||
chr2:58136314
|
A | C | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.856+1115A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136314 | ||||||
chr2:58136388
|
A | AT | 18 | a0001c0001t0002g0014a0001c0003t0001g0007a0001c0003t0001g0008others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.856+1203dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136388 | |||||
chr2:58136388
|
AT | A | 29 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(26): Show | 29 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.856+1203delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136388 | |||||
chr2:58136421
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.856+1222G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136421 | ||||||
chr2:58136486
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.856+1287G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136486 | ||||||
chr2:58136569
|
G | C | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.856+1370G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136569 | ||||||
chr2:58136594
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.856+1395A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136594 | ||||||
chr2:58136648
|
G | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG03041.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1449G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136648 | ||||||
chr2:58136763
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0099 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.856+1602_856+1622d others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136763 | |||||
chr2:58136763
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0309a0001c0001t0002g0002 | 3 | HG01168.hp1 HG01169.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.856+1602_856+1622d others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136763 | |||||
chr2:58136794
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.856+1595C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136794 | ||||||
chr2:58136830
|
ATATATCA others(7): Show |
A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1646_856+1659d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136830 | |||||
chr2:58136831
|
T | G | 2 | a0002c0002t0002g0041a0002c0002t0002g0068 | 2 | NA18945.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.856+1632T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136831 | ||||||
chr2:58136839
|
ATATAT | A | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1646_856+1650d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136839 | |||||
chr2:58136844
|
TTA | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0167 | 3 | HG02280.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.856+1649_856+1650d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136844 | |||||
chr2:58136847
|
TATC | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1651_856+1653d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136847 | |||||
chr2:58136857
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1658A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136857 | ||||||
chr2:58136865
|
ATATATCA others(5): Show |
A | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1679_856+1690d others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136865 | |||||
chr2:58136871
|
C | CAT | 159 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.856+1677_856+1678d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136871 | |||||
chr2:58136871
|
C | CATATATA others(28): Show |
1 | a0001c0001t0001g0307 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.856+1678_856+1679i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136871 | |||||
chr2:58136878
|
T | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1679T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136878 | ||||||
chr2:58136883
|
C | A | 1 | a0002c0002t0002g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1684C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136883 | ||||||
chr2:58136884
|
A | T | 1 | a0002c0002t0002g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1685A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136884 | ||||||
chr2:58136885
|
T | C | 1 | a0002c0002t0002g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1686T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136885 | ||||||
chr2:58136891
|
TGTGTA | T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1693_856+1697d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136891 | ||||||
chr2:58136894
|
G | A | 1 | a0002c0002t0002g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1695G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136894 | ||||||
chr2:58136896
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0002g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1714_856+1741d others(30): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136896 | |||||
chr2:58136906
|
TATATATA others(2): Show |
T | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1714_856+1722d others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136906 | |||||
chr2:58136907
|
A | ATATAT | 289 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.856+1709_856+1713d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | |||||
chr2:58136907
|
A | ATATATTA others(33): Show |
7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+1713_856+1714i others(42): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | |||||
chr2:58136907
|
A | ATATTATA others(28): Show |
1 | a0002c0002t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.856+1711_856+1712i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | |||||
chr2:58136909
|
A | ATAT | 15 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.856+1711_856+1713d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136909 | |||||
chr2:58136915
|
C | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1716C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136915 | ||||||
chr2:58136915
|
C | CAT | 28 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(25): Show | 28 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.856+1721_856+1722d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136915 | |||||
chr2:58136916
|
A | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1717A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136916 | ||||||
chr2:58136917
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1718T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136917 | ||||||
chr2:58136917
|
T | TATATATG others(28): Show |
1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.856+1722_856+1723i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136917 | |||||
chr2:58136932
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1733C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136932 | ||||||
chr2:58136933
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1734A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136933 | ||||||
chr2:58136934
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1735T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136934 | ||||||
chr2:58136940
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.856+1741T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136940 | ||||||
chr2:58136965
|
A | C | 1 | a0001c0001t0002g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1766A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136965 | ||||||
chr2:58136966
|
T | A | 1 | a0001c0001t0002g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1767T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136966 | ||||||
chr2:58136967
|
C | CAT | 14 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.856+1773_856+1774d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136967 | |||||
chr2:58136967
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1768C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136967 | ||||||
chr2:58137007
|
ATT | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1809_856+1810d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137007 | ||||||
chr2:58137078
|
A | T | 36 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.856+1879A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137078 | ||||||
chr2:58137079
|
CAT | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.856+1887_856+1888d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137079 | |||||
chr2:58137081
|
T | TATATGTG others(26): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02015.hp2 NA18747.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.856+1886_856+1887i others(35): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137081 | |||||
chr2:58137099
|
A | T | 1 | a0002c0002t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.856+1900A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137099 | ||||||
chr2:58137156
|
T | TTATATAT others(22): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(31): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137156 | |||||
chr2:58137156
|
TTA | T | 7 | a0001c0001t0001g0054a0001c0003t0001g0264a0001c0003t0001g0266others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+1965_856+1966d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137156 | |||||
chr2:58137158
|
A | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.856+1959A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137158 | ||||||
chr2:58137165
|
T | TCATATAT others(4): Show |
1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137165 | |||||
chr2:58137166
|
C | CAT | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0003t0001g0271others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1972_856+1973d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137166 | |||||
chr2:58137172
|
T | TATCATAT others(121): Show |
1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(130): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | ||||||
chr2:58137172
|
T | TATCATAT others(99): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(108): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | ||||||
chr2:58137172
|
T | TATCATAT others(119): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02280.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | ||||||
chr2:58137172
|
T | TATCATAT others(119): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02647.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | ||||||
chr2:58137172
|
T | TATCATAT others(119): Show |
1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | ||||||
chr2:58137172
|
T | TCATATAT others(176): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0121a0007c0009t0001g0122 | 3 | HG03195.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(185): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137172
|
T | TCATATAT others(196): Show |
3 | a0001c0001t0001g0119a0003c0005t0001g0114a0003c0005t0001g0115 | 3 | HG02109.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(205): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137172
|
T | TCATATAT others(216): Show |
4 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0120others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(225): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137172
|
T | TCATATAT others(236): Show |
1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(245): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137172
|
T | TCATATAT others(198): Show |
1 | a0001c0001t0001g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(207): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137172
|
T | TCATATAT others(194): Show |
1 | a0001c0001t0001g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(203): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | |||||
chr2:58137178
|
A | ATATCATA others(144): Show |
1 | a0002c0002t0002g0229 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(153): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137178 | |||||
chr2:58137180
|
A | ATC | 11 | a0001c0001t0001g0015a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.856+1982_856+1983d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(180): Show |
1 | a0001c0001t0001g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(189): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(134): Show |
1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(143): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(234): Show |
1 | a0001c0004t0001g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(212): Show |
1 | a0001c0004t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
1 | a0001c0001t0001g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(163): Show |
1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(185): Show |
16 | a0001c0001t0001g0059a0001c0001t0001g0124a0001c0001t0001g0125others(13): Show | 16 | HG00099.hp1 HG01109.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(207): Show |
1 | a0001c0001t0001g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(216): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(141): Show |
6 | a0001c0001t0001g0291a0001c0001t0001g0298a0001c0001t0001g0303others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(163): Show |
1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(185): Show |
1 | a0001c0001t0001g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(141): Show |
6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0304others(3): Show | 6 | HG00438.hp1 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(163): Show |
8 | a0001c0001t0001g0117a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG00323.hp2 HG00597.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(115): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0150 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(124): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(203): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0277 | 2 | HG02886.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(212): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(181): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(8): Show | 12 | HG01928.hp2 NA18945.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(159): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0284 | 2 | HG03654.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(168): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(181): Show |
4 | a0001c0001t0001g0180a0001c0001t0001g0219a0001c0001t0001g0238others(1): Show | 4 | NA18964.hp2 NA18977.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(181): Show |
1 | a0001c0001t0001g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(195): Show |
1 | a0001c0001t0001g0280 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(204): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(289): Show |
1 | a0001c0001t0001g0287 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(298): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(139): Show |
4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(148): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(179): Show |
1 | a0001c0001t0001g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(188): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(170): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(179): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(212): Show |
1 | a0001c0001t0001g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(256): Show |
1 | a0001c0001t0001g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(265): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
15 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0051others(12): Show | 15 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG04199.hp1 NA18971.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0294 | 2 | HG01496.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(146): Show |
2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(140): Show |
2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(149): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(162): Show |
1 | a0004c0010t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(171): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(227): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0141 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(236): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(173): Show |
1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+2002_856+2003i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(195): Show |
1 | a0001c0001t0001g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856+2002_856+2003i others(204): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(92): Show |
1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.856+2002_856+2003i others(101): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(114): Show |
1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.856+2002_856+2003i others(123): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
5 | a0001c0001t0002g0004a0001c0001t0002g0173a0001c0001t0002g0175others(2): Show | 6 | NA18955.hp1 NA18969.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0016 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(222): Show |
1 | a0002c0002t0002g0075 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(231): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(217): Show |
4 | a0001c0001t0002g0181a0001c0001t0002g0195a0001c0001t0002g0196others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(217): Show |
1 | a0001c0001t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(173): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0255 | 2 | HG02615.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(170): Show |
1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(179): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
4 | a0001c0001t0002g0170a0001c0001t0002g0240a0001c0001t0002g0241others(1): Show | 4 | HG02165.hp1 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(212): Show |
2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(234): Show |
1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
26 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0038others(23): Show | 28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
10 | a0001c0001t0002g0174a0001c0001t0002g0185a0001c0001t0002g0211others(7): Show | 10 | HG00280.hp2 HG00735.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(212): Show |
3 | a0001c0001t0002g0187a0001c0001t0002g0210a0001c0001t0003g0244 | 3 | HG02145.hp2 HG02698.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(166): Show |
1 | a0001c0001t0002g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(175): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
1 | a0002c0002t0002g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
2 | a0002c0002t0002g0019a0002c0002t0002g0071 | 2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
1 | a0002c0002t0002g0020 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(206): Show |
1 | a0001c0001t0002g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(215): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
1 | a0001c0001t0002g0225 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(188): Show |
1 | a0001c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(168): Show |
2 | a0001c0001t0002g0002a0001c0001t0002g0168 | 3 | HG01168.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(141): Show |
1 | a0001c0001t0002g0205 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137180
|
A | ATCATATA others(185): Show |
1 | a0001c0001t0002g0172 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | |||||
chr2:58137182
|
C | CATATATA others(416): Show |
1 | a0001c0001t0001g0331 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(425): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(370): Show |
1 | a0001c0001t0001g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(379): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(302): Show |
1 | a0001c0001t0001g0327 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(311): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(324): Show |
1 | a0001c0001t0001g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(333): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(324): Show |
1 | a0001c0001t0001g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(333): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(280): Show |
1 | a0001c0001t0001g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(289): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(262): Show |
3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG01891.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(271): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(278): Show |
2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(287): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(278): Show |
1 | a0001c0001t0001g0324 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(287): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(412): Show |
1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(421): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(390): Show |
1 | a0001c0001t0001g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(399): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(390): Show |
1 | a0001c0001t0001g0319 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(399): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(250): Show |
1 | a0001c0001t0001g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(259): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(254): Show |
1 | a0001c0001t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(263): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(254): Show |
1 | a0001c0001t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(263): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(346): Show |
1 | a0001c0003t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(355): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(456): Show |
1 | a0001c0003t0001g0260 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(465): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATA others(386): Show |
1 | a0001c0003t0001g0259 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(395): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(175): Show |
1 | a0002c0002t0002g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(184): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(67): Show |
1 | a0002c0002t0002g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(76): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(247): Show |
1 | a0002c0002t0002g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(256): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(200): Show |
4 | a0002c0002t0002g0041a0002c0002t0002g0068a0002c0002t0002g0072others(1): Show | 4 | HG01975.hp2 HG02293.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(200): Show |
1 | a0002c0002t0002g0069 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(177): Show |
1 | a0002c0002t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(186): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(199): Show |
1 | a0002c0002t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(208): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(129): Show |
1 | a0002c0002t0002g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(138): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(173): Show |
10 | a0002c0002t0002g0001a0002c0002t0002g0044a0002c0002t0002g0057others(7): Show | 11 | HG00323.hp1 HG00621.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(200): Show |
1 | a0002c0002t0002g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(166): Show |
2 | a0002c0002t0002g0076a0002c0002t0002g0077 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(175): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(188): Show |
1 | a0002c0002t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(122): Show |
1 | a0002c0002t0002g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(131): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(80): Show |
1 | a0002c0002t0002g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(89): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(102): Show |
2 | a0002c0002t0002g0079a0002c0002t0002g0100 | 2 | HG01496.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(111): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(146): Show |
28 | a0001c0001t0002g0014a0002c0002t0002g0026a0002c0002t0002g0027others(25): Show | 28 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(168): Show |
4 | a0002c0002t0002g0089a0002c0002t0002g0103a0002c0002t0002g0159others(1): Show | 4 | HG00558.hp2 HG00621.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(190): Show |
1 | a0002c0002t0005g0104 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(234): Show |
1 | a0002c0002t0002g0080 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(146): Show |
1 | a0002c0002t0002g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(168): Show |
1 | a0002c0002t0002g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(104): Show |
1 | a0002c0002t0002g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(113): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(173): Show |
2 | a0002c0002t0002g0234a0006c0008t0002g0235 | 2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(80): Show |
1 | a0002c0002t0002g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(89): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(146): Show |
5 | a0002c0002t0002g0230a0002c0002t0002g0231a0002c0002t0002g0232others(2): Show | 5 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(186): Show |
1 | a0002c0002t0002g0333 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(195): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
C | CATATATG others(119): Show |
1 | a0002c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137182
|
CATATATG others(6): Show |
C | 6 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+1990_856+2002d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | |||||
chr2:58137184
|
T | TATATGAT others(208): Show |
1 | a0001c0001t0002g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(217): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137184 | |||||
chr2:58137188
|
T | TATCATAT others(62): Show |
7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(71): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137188 | ||||||
chr2:58137193
|
C | T | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.856+1994C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137193 | ||||||
chr2:58137193
|
CAT | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+2001_856+2002d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137193 | |||||
chr2:58137195
|
T | TATATCAT others(171): Show |
2 | a0002c0002t0002g0039a0002c0002t0002g0040 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(180): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137195 | |||||
chr2:58137195
|
T | TATATCAT others(193): Show |
1 | a0002c0002t0002g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(202): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137195 | |||||
chr2:58137195
|
T | TGTATCAT others(11): Show |
2 | a0001c0003t0001g0271a0001c0003t0001g0272 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.856+1996_856+1997i others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137195 | ||||||
chr2:58137198
|
A | ATCATATA others(217): Show |
1 | a0002c0002t0002g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | |||||
chr2:58137198
|
A | ATCATATA others(188): Show |
1 | a0002c0002t0002g0257 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | |||||
chr2:58137198
|
A | ATCATATA others(102): Show |
1 | a0002c0002t0002g0087 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(111): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | |||||
chr2:58137198
|
A | ATCATATA others(183): Show |
1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(192): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | |||||
chr2:58137198
|
A | G | 9 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(6): Show | 9 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+1999A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137198 | ||||||
chr2:58137200
|
ATC | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+2004_856+2005d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137200 | |||||
chr2:58137202
|
C | A | 19 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0290others(16): Show | 19 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.856+2003C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137202 | ||||||
chr2:58137203
|
T | A | 32 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(29): Show | 32 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.856+2004T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137203 | ||||||
chr2:58137204
|
C | T | 32 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(29): Show | 32 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.856+2005C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137204 | ||||||
chr2:58137218
|
A | G | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2019A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137218 | ||||||
chr2:58137220
|
A | G | 4 | a0002c0002t0002g0063a0002c0002t0002g0087a0002c0002t0002g0088others(1): Show | 4 | HG01255.hp2 HG01361.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2021A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137220 | ||||||
chr2:58137221
|
T | TC | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2022_856+2023i others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137221 | ||||||
chr2:58137222
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+2023A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137222 | ||||||
chr2:58137223
|
T | TA | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2024_856+2025i others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137223 | ||||||
chr2:58137224
|
C | CAT | 222 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.856+2028_856+2029d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | |||||
chr2:58137224
|
C | CATAT | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.856+2026_856+2029d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | |||||
chr2:58137224
|
C | CATATGAT others(13): Show |
1 | a0001c0001t0001g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.856+2030_856+2049d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | |||||
chr2:58137224
|
C | CTCAT | 5 | a0001c0001t0002g0207a0002c0002t0002g0042a0002c0002t0002g0087others(2): Show | 5 | HG01433.hp2 HG02165.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.856+2025_856+2026i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | ||||||
chr2:58137224
|
C | CTCATATA others(17): Show |
1 | a0002c0002t0002g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+2025_856+2026i others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | ||||||
chr2:58137224
|
C | T | 9 | a0001c0001t0001g0029a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+2025C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | ||||||
chr2:58137224
|
CAT | C | 4 | a0001c0001t0002g0181a0001c0001t0002g0195a0001c0001t0002g0196others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2028_856+2029d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | |||||
chr2:58137233
|
CAT | C | 6 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2041_856+2042d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137233 | |||||
chr2:58137238
|
A | G | 6 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2039A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137238 | ||||||
chr2:58137242
|
C | CATATATG others(62): Show |
1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+2049_856+2050i others(71): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137242 | |||||
chr2:58137242
|
CATATATA others(11): Show |
C | 2 | a0001c0003t0001g0271a0001c0003t0001g0272 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.856+2053_856+2070d others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137242 | |||||
chr2:58137251
|
G | GATAC | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.856+2055_856+2056i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137251 | |||||
chr2:58137255
|
T | C | 22 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(19): Show | 22 | HG01891.hp2 HG02071.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.856+2056T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137255 | ||||||
chr2:58137260
|
G | C | 6 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2061G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137260 | ||||||
chr2:58137318
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.856+2119G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137318 | ||||||
chr2:58137495
|
A | G | 1 | a0002c0002t0002g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.857-2171A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137495 | ||||||
chr2:58137530
|
A | G | 3 | a0001c0003t0001g0270a0001c0003t0001g0273a0001c0003t0001g0275 | 3 | HG01884.hp2 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.857-2136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137530 | ||||||
chr2:58137607
|
T | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(70): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.857-2059T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137607 | ||||||
chr2:58137618
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.857-2048G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137618 | ||||||
chr2:58137691
|
C | G | 1 | a0001c0001t0002g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.857-1975C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137691 | ||||||
chr2:58137803
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.857-1863T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137803 | ||||||
chr2:58137915
|
T | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1751T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137915 | ||||||
chr2:58137916
|
A | C | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1750A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137916 | ||||||
chr2:58137917
|
C | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1749C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137917 | ||||||
chr2:58137919
|
C | T | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1747C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137919 | ||||||
chr2:58137920
|
T | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1746T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137920 | ||||||
chr2:58137922
|
C | T | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1744C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137922 | ||||||
chr2:58137923
|
A | G | 9 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.857-1743A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137923 | ||||||
chr2:58137924
|
G | C | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1742G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137924 | ||||||
chr2:58137925
|
G | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137925 | ||||||
chr2:58137927
|
T | A | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1739T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137927 | ||||||
chr2:58138015
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.857-1651C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138015 | ||||||
chr2:58138215
|
A | C | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.857-1451A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138215 | ||||||
chr2:58138408
|
C | T | 1 | a0002c0002t0002g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.857-1258C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138408 | ||||||
chr2:58138444
|
A | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.857-1222A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138444 | ||||||
chr2:58138540
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.857-1126G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138540 | ||||||
chr2:58138574
|
C | T | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.857-1092C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138574 | ||||||
chr2:58138760
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.857-906T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138760 | ||||||
chr2:58138841
|
A | G | 1 | a0002c0002t0002g0044 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.857-825A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138841 | ||||||
chr2:58138906
|
T | C | 1 | a0002c0002t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.857-760T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138906 | ||||||
chr2:58138987
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.857-679A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138987 | ||||||
chr2:58139373
|
A | C | 1 | a0002c0002t0002g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.857-293A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139373 | ||||||
chr2:58139384
|
T | G | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.857-282T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139384 | ||||||
chr2:58139468
|
A | T | 1 | a0001c0001t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.857-198A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139468 | ||||||
chr2:58139543
|
T | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.857-123T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139543 | ||||||
chr2:58139957
|
T | C | 36 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023+125T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58139957 | ||||||
chr2:58140003
|
G | A | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1023+171G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140003 | ||||||
chr2:58140060
|
G | A | 1 | a0002c0002t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1023+228G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140060 | ||||||
chr2:58140269
|
TACA | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+438_1023+440d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140269 | ||||||
chr2:58140273
|
G | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+441G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140273 | ||||||
chr2:58140360
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1023+528C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140360 | ||||||
chr2:58140917
|
C | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0253 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1023+1085C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140917 | ||||||
chr2:58140986
|
C | T | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1023+1154C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140986 | ||||||
chr2:58141071
|
TTTAATAA others(6): Show |
T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1023+1240_1023+125 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141071 | ||||||
chr2:58141275
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1023+1443A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141275 | ||||||
chr2:58141520
|
G | A | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1023+1688G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141520 | ||||||
chr2:58141684
|
T | C | 8 | a0001c0003t0001g0264a0001c0003t0001g0266a0001c0003t0001g0270others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1852T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141684 | ||||||
chr2:58141703
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1023+1871T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141703 | ||||||
chr2:58141740
|
T | G | 2 | a0001c0001t0002g0241a0001c0001t0002g0242 | 2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1023+1908T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141740 | ||||||
chr2:58141832
|
C | T | 1 | a0001c0003t0001g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1023+2000C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141832 | ||||||
chr2:58141849
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1023+2017A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141849 | ||||||
chr2:58142108
|
C | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1023+2276C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142108 | ||||||
chr2:58142170
|
A | T | 1 | a0002c0002t0002g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1023+2338A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142170 | ||||||
chr2:58142197
|
A | C | 1 | a0001c0001t0001g0308 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1023+2365A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142197 | ||||||
chr2:58142324
|
G | GT | 21 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1023+2506dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58142324 | |||||
chr2:58142920
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1023+3088C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142920 | ||||||
chr2:58143077
|
A | G | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024-3239A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143077 | ||||||
chr2:58143207
|
T | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0228 | 2 | HG02027.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1024-3109T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143207 | ||||||
chr2:58143312
|
A | G | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-3004A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143312 | ||||||
chr2:58143403
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1024-2913G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143403 | ||||||
chr2:58143412
|
A | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1024-2904A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143412 | ||||||
chr2:58143481
|
T | C | 21 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-2835T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143481 | ||||||
chr2:58143588
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1024-2728T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143588 | ||||||
chr2:58143614
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1024-2702G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143614 | ||||||
chr2:58143630
|
G | C | 25 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1024-2686G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143630 | ||||||
chr2:58143945
|
T | C | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024-2371T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143945 | ||||||
chr2:58143968
|
T | C | 2 | a0001c0001t0002g0198a0001c0001t0002g0205 | 2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1024-2348T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143968 | ||||||
chr2:58144010
|
T | C | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2306T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144010 | ||||||
chr2:58144012
|
T | C | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2304T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144012 | ||||||
chr2:58144018
|
T | C | 90 | a0001c0001t0002g0014a0002c0002t0001g0152a0002c0002t0001g0153others(87): Show | 91 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1024-2298T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144018 | ||||||
chr2:58144034
|
T | C | 11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1024-2282T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144034 | ||||||
chr2:58144222
|
C | T | 21 | a0001c0001t0001g0277a0001c0001t0001g0288a0001c0001t0001g0289others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-2094C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144222 | ||||||
chr2:58144233
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-2083G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144233 | ||||||
chr2:58144275
|
T | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-2041T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144275 | ||||||
chr2:58144331
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1024-1985G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144331 | ||||||
chr2:58144921
|
C | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1024-1395C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144921 | ||||||
chr2:58145008
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | NA19001.hp1 NA19057.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-1308T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145008 | ||||||
chr2:58145016
|
T | C | 16 | a0001c0001t0001g0145a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1024-1300T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145016 | ||||||
chr2:58145040
|
C | G | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1024-1276C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145040 | ||||||
chr2:58145214
|
G | A | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1024-1102G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145214 | ||||||
chr2:58145319
|
C | T | 20 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1024-997C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145319 | ||||||
chr2:58145321
|
A | G | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-995A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145321 | ||||||
chr2:58145348
|
C | T | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1024-968C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145348 | ||||||
chr2:58145368
|
CA | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(14): Show | 17 | HG01928.hp2 HG01934.hp2 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.1024-943delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58145368 | |||||
chr2:58145455
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1024-861A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145455 | ||||||
chr2:58145459
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(62): Show | 66 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.1024-857G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145459 | ||||||
chr2:58145540
|
A | G | 1 | a0002c0002t0002g0334 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1024-776A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145540 | ||||||
chr2:58145542
|
T | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1024-774T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145542 | ||||||
chr2:58145553
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-763A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145553 | ||||||
chr2:58145626
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-690A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145626 | ||||||
chr2:58145681
|
TTATTACA | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-631_1024-625d others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58145681 | |||||
chr2:58145779
|
C | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-537C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145779 | ||||||
chr2:58145781
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1024-535C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145781 | ||||||
chr2:58145843
|
A | G | 52 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(49): Show | 52 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024-473A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145843 | ||||||
chr2:58146018
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1024-298A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146018 | ||||||
chr2:58146050
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-266C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146050 | ||||||
chr2:58146070
|
C | T | 77 | a0001c0001t0002g0014a0002c0002t0001g0256a0002c0002t0002g0001others(74): Show | 78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1024-246C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146070 | ||||||
chr2:58146146
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-170T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146146 | ||||||
chr2:58146156
|
G | A | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024-160G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146156 | ||||||
chr2:58146165
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-151T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146165 | ||||||
chr2:58146312
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.1024-4A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146312 | ||||||
chr2:58146489
|
T | C | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1182+15T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146489 | ||||||
chr2:58146619
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1182+145G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146619 | ||||||
chr2:58146631
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1182+157A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146631 | ||||||
chr2:58146637
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1182+163G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146637 | ||||||
chr2:58146733
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1182+259T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146733 | ||||||
chr2:58146767
|
ATG | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(37): Show | 41 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1182+295_1182+296d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58146767 | |||||
chr2:58146769
|
GTA | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02015.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1182+297_1182+298d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58146769 | |||||
chr2:58146801
|
C | G | 5 | a0001c0001t0001g0145a0001c0003t0001g0270a0001c0003t0001g0273others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+327C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146801 | ||||||
chr2:58147121
|
C | G | 1 | a0001c0001t0002g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1182+647C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147121 | ||||||
chr2:58147258
|
A | G | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+784A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147258 | ||||||
chr2:58147563
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1089G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147563 | ||||||
chr2:58147610
|
A | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147610 | ||||||
chr2:58147658
|
TTTCCC | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+1186_1182+119 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147658 | |||||
chr2:58147664
|
T | A | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+1190T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147664 | ||||||
chr2:58147797
|
A | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182+1323A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147797 | ||||||
chr2:58147800
|
G | GT | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0130others(5): Show | 8 | HG01070.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182+1342dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147800 | |||||
chr2:58147800
|
GT | G | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1182+1342delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147800 | |||||
chr2:58147877
|
T | G | 7 | a0001c0001t0001g0145a0001c0003t0001g0270a0001c0003t0001g0271others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+1403T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147877 | ||||||
chr2:58147896
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1182+1422A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147896 | ||||||
chr2:58148120
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1182+1646T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148120 | ||||||
chr2:58148187
|
A | G | 11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+1713A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148187 | ||||||
chr2:58148221
|
T | A | 322 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(319): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1182+1747T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148221 | ||||||
chr2:58148251
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1182+1777G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148251 | ||||||
chr2:58148258
|
A | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1784A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148258 | ||||||
chr2:58148427
|
T | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+1953T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148427 | ||||||
chr2:58148553
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(78): Show | 82 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(79): Show |
intron_variant | MODIFIER | c.1182+2079C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148553 | ||||||
chr2:58148716
|
G | C | 1 | a0001c0001t0002g0188 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182+2242G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148716 | ||||||
chr2:58148839
|
A | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+2365A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148839 | ||||||
chr2:58148850
|
T | C | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1182+2376T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148850 | ||||||
chr2:58148899
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+2425G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148899 | ||||||
chr2:58149178
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0258 | 2 | HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1182+2704C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149178 | ||||||
chr2:58149452
|
G | C | 1 | a0002c0002t0002g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1182+2978G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149452 | ||||||
chr2:58149456
|
T | C | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+2982T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149456 | ||||||
chr2:58149746
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1182+3272A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149746 | ||||||
chr2:58149871
|
A | G | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3397A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149871 | ||||||
chr2:58149879
|
T | C | 175 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1182+3405T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149879 | ||||||
chr2:58149888
|
A | T | 175 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1182+3414A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149888 | ||||||
chr2:58149991
|
CTTTTCTT others(5): Show |
C | 3 | a0001c0001t0001g0006a0001c0001t0001g0278a0001c0001t0001g0279 | 4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3522_1182+353 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149991 | |||||
chr2:58149996
|
CT | C | 223 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1182+3540delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149996 | |||||
chr2:58149996
|
CTTT | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+3538_1182+354 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149996 | |||||
chr2:58150097
|
G | A | 1 | a0002c0002t0002g0234 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1182+3623G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150097 | ||||||
chr2:58150156
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1182+3682T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150156 | ||||||
chr2:58150206
|
G | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+3732G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150206 | ||||||
chr2:58150308
|
A | AT | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+3842dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150308 | |||||
chr2:58150561
|
A | G | 2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1182+4087A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150561 | ||||||
chr2:58150561
|
A | T | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1182+4087A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150561 | ||||||
chr2:58150562
|
GT | G | 136 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(133): Show | 137 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(134): Show |
intron_variant | MODIFIER | c.1182+4102delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150562 | |||||
chr2:58150563
|
T | TTTTTTTT others(6): Show |
2 | a0001c0003t0001g0264a0001c0003t0001g0266 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1182+4100_1182+410 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150563 | |||||
chr2:58150565
|
T | G | 1 | a0001c0003t0001g0259 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182+4091T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150565 | ||||||
chr2:58150756
|
G | A | 115 | a0001c0001t0001g0117a0001c0001t0001g0277a0001c0001t0001g0281others(112): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1182+4282G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150756 | ||||||
chr2:58150942
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1182+4468C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150942 | ||||||
chr2:58150942
|
CTTT | C | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182+4472_1182+447 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150942 | |||||
chr2:58151006
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1182+4532T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151006 | ||||||
chr2:58151080
|
A | C | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182+4606A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151080 | ||||||
chr2:58151251
|
A | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+4777A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151251 | ||||||
chr2:58151502
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1182+5028G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151502 | ||||||
chr2:58151526
|
A | C | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+5052A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151526 | ||||||
chr2:58151572
|
TCCATTTC others(38): Show |
T | 1 | a0002c0002t0002g0232 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1182+5104_1182+514 others(49): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151572 | |||||
chr2:58151731
|
G | GT | 34 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0056others(31): Show | 35 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1182+5293dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTT | 31 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0118others(28): Show | 32 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1182+5292_1182+529 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTT | 12 | a0001c0001t0001g0262a0001c0001t0001g0316a0001c0001t0001g0317others(9): Show | 12 | HG00741.hp1 HG01433.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1182+5291_1182+529 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTT | 6 | a0001c0001t0001g0251a0001c0001t0001g0322a0001c0001t0001g0328others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5290_1182+529 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT | 11 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0099others(8): Show | 11 | HG00558.hp2 HG01261.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+5287_1182+529 others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(1): Show |
14 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0180others(11): Show | 14 | HG01255.hp2 HG01433.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1182+5286_1182+529 others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(2): Show |
19 | a0001c0001t0001g0030a0001c0001t0001g0293a0001c0003t0001g0260others(16): Show | 20 | HG00621.hp1 HG00621.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1182+5285_1182+529 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(3): Show |
21 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1182+5284_1182+529 others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(4): Show |
6 | a0001c0001t0001g0046a0001c0001t0001g0238a0002c0002t0002g0098others(3): Show | 6 | HG02886.hp2 NA18940.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5283_1182+529 others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(5): Show |
6 | a0001c0001t0001g0052a0002c0002t0002g0049a0002c0002t0002g0061others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5282_1182+529 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0025a0002c0002t0002g0060a0002c0002t0002g0088others(3): Show | 6 | HG02027.hp1 NA18747.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5281_1182+529 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(7): Show |
5 | a0001c0001t0001g0166a0002c0002t0002g0227a0002c0002t0002g0231others(2): Show | 5 | HG01167.hp1 HG01256.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182+5280_1182+529 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0047a0001c0001t0001g0054a0002c0002t0002g0042others(1): Show | 4 | HG02074.hp2 NA18973.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5279_1182+529 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0162a0001c0003t0001g0259a0002c0002t0001g0153others(1): Show | 4 | HG02071.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5278_1182+529 others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0282a0002c0002t0002g0243 | 3 | HG02165.hp2 HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1182+5277_1182+529 others(21): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(11): Show |
4 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0283others(1): Show | 4 | HG03453.hp2 NA18971.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+5276_1182+529 others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(12): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0183a0001c0001t0001g0312others(1): Show | 4 | HG02040.hp1 HG03540.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5275_1182+529 others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0167 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1182+5273_1182+529 others(25): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0281 | 2 | HG03041.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1182+5272_1182+529 others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182+5270_1182+529 others(28): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GT | G | 7 | a0001c0001t0002g0189a0001c0001t0003g0247a0001c0001t0003g0248others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+5293delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTT | G | 16 | a0001c0001t0001g0145a0001c0001t0001g0289a0001c0001t0001g0302others(13): Show | 16 | HG00597.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1182+5291_1182+529 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTT | G | 23 | a0001c0001t0001g0288a0001c0001t0001g0291a0001c0001t0001g0296others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1182+5290_1182+529 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTT | G | 10 | a0001c0001t0001g0179a0001c0001t0001g0265a0001c0001t0001g0267others(7): Show | 10 | HG00738.hp1 HG01243.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182+5288_1182+529 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(2): Show |
G | 26 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0123others(23): Show | 26 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1182+5285_1182+529 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(4): Show |
G | 1 | a0002c0002t0002g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1182+5283_1182+529 others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1182+5281_1182+529 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(7): Show |
G | 4 | a0002c0002t0002g0026a0002c0002t0002g0027a0002c0002t0002g0058others(1): Show | 4 | HG01496.hp1 HG02738.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5280_1182+529 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1182+5279_1182+529 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG02886.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1182+5278_1182+529 others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151731
|
GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0001g0015a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+5275_1182+529 others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | |||||
chr2:58151739
|
T | C | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1182+5265T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151739 | ||||||
chr2:58151740
|
T | C | 5 | a0001c0003t0001g0010a0001c0003t0001g0013a0001c0003t0004g0009others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+5266T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151740 | ||||||
chr2:58151744
|
T | TTTTTTTT others(13): Show |
1 | a0001c0001t0001g0029 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1182+5289_1182+529 others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151744 | |||||
chr2:58151746
|
T | G | 1 | a0002c0002t0002g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1182+5272T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151746 | ||||||
chr2:58151769
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1182+5295G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151769 | ||||||
chr2:58151807
|
C | T | 109 | a0001c0001t0001g0277a0001c0001t0001g0288a0001c0001t0001g0289others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1182+5333C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151807 | ||||||
chr2:58151883
|
A | C | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1182+5409A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151883 | ||||||
chr2:58151939
|
G | A | 1 | a0008c0006t0002g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1182+5465G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151939 | ||||||
chr2:58152035
|
A | C | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0004c0010t0001g0151 | 3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+5561A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152035 | ||||||
chr2:58152284
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+5810G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152284 | ||||||
chr2:58152361
|
A | C | 260 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1182+5887A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152361 | ||||||
chr2:58152385
|
T | A | 88 | a0001c0001t0002g0014a0002c0002t0001g0256a0002c0002t0002g0001others(85): Show | 89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1182+5911T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152385 | ||||||
chr2:58152694
|
A | AT | 10 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0173others(7): Show | 11 | HG00423.hp1 NA18955.hp1 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+6229dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58152694 | |||||
chr2:58152876
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1182+6402C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152876 | ||||||
chr2:58153032
|
G | A | 174 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1183-6317G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153032 | ||||||
chr2:58153134
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1183-6215T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153134 | ||||||
chr2:58153155
|
A | G | 16 | a0001c0001t0001g0145a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-6194A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153155 | ||||||
chr2:58153166
|
G | T | 20 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1183-6183G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153166 | ||||||
chr2:58153279
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1183-6070T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153279 | ||||||
chr2:58153386
|
C | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG02145.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-5963C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153386 | ||||||
chr2:58153516
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1183-5833G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153516 | ||||||
chr2:58153523
|
G | C | 88 | a0001c0001t0002g0014a0002c0002t0001g0256a0002c0002t0002g0001others(85): Show | 89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1183-5826G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153523 | ||||||
chr2:58153586
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1183-5763C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153586 | ||||||
chr2:58153613
|
G | A | 2 | a0001c0001t0001g0121a0007c0009t0001g0122 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1183-5736G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153613 | ||||||
chr2:58153693
|
G | T | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-5656G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153693 | ||||||
chr2:58153832
|
G | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1183-5517G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153832 | ||||||
chr2:58154070
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1183-5279A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154070 | ||||||
chr2:58154242
|
A | T | 16 | a0001c0001t0001g0145a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-5107A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154242 | ||||||
chr2:58154256
|
A | AT | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-5087dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58154256 | |||||
chr2:58154277
|
T | G | 11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-5072T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154277 | ||||||
chr2:58154321
|
CT | C | 32 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 32 | HG01099.hp2 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1183-5018delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58154321 | |||||
chr2:58154371
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1183-4978T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154371 | ||||||
chr2:58154615
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-4734G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154615 | ||||||
chr2:58154650
|
T | C | 72 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(69): Show | 76 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1183-4699T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154650 | ||||||
chr2:58154704
|
A | C | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1183-4645A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154704 | ||||||
chr2:58155011
|
T | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0305 | 2 | NA18971.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1183-4338T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155011 | ||||||
chr2:58155079
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1183-4270T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155079 | ||||||
chr2:58155355
|
G | A | 188 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(185): Show | 193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1183-3994G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155355 | ||||||
chr2:58155488
|
T | TGGGAAGT others(2): Show |
11 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-3861_1183-386 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155488 | ||||||
chr2:58155556
|
A | C | 62 | a0001c0001t0001g0059a0001c0001t0001g0117a0001c0001t0001g0123others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1183-3793A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155556 | ||||||
chr2:58155579
|
A | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-3770A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155579 | ||||||
chr2:58155613
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0306 | 2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1183-3736C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155613 | ||||||
chr2:58155766
|
A | C | 1 | a0002c0002t0002g0155 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1183-3583A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155766 | ||||||
chr2:58155917
|
G | GT | 10 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1183-3429dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155917 | |||||
chr2:58155917
|
G | GTT | 11 | a0001c0001t0001g0145a0001c0001t0001g0252a0001c0001t0001g0253others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-3430_1183-342 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155917 | |||||
chr2:58155920
|
TG | T | 15 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(12): Show | 15 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1183-3428delG | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155920 | ||||||
chr2:58155921
|
G | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(70): Show | 74 | HG00423.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1183-3428G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155921 | ||||||
chr2:58155921
|
GT | G | 77 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0304others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1183-3415delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155921 | |||||
chr2:58155925
|
T | G | 14 | a0001c0001t0001g0015a0001c0001t0001g0146a0001c0001t0001g0147others(11): Show | 14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-3424T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155925 | ||||||
chr2:58155946
|
A | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0143 | 2 | HG02300.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1183-3403A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155946 | ||||||
chr2:58155954
|
G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0112others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-3395G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155954 | ||||||
chr2:58156140
|
G | GC | 10 | a0001c0001t0001g0117a0001c0001t0001g0163a0001c0001t0001g0164others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183-3205dupC | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156140 | |||||
chr2:58156141
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1183-3208C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156141 | ||||||
chr2:58156160
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1183-3189A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156160 | ||||||
chr2:58156171
|
A | G | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1183-3178A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156171 | ||||||
chr2:58156263
|
T | C | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-3086T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156263 | ||||||
chr2:58156366
|
C | T | 1 | a0001c0001t0002g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1183-2983C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156366 | ||||||
chr2:58156579
|
GTTTTT | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0265others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-2766_1183-276 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156579 | |||||
chr2:58156580
|
T | G | 16 | a0001c0001t0001g0145a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-2769T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156580 | ||||||
chr2:58156583
|
T | A | 1 | a0003c0005t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1183-2766T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156583 | ||||||
chr2:58156583
|
T | TTTTTGTT others(8): Show |
1 | a0001c0001t0002g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1183-2746_1183-273 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156583 | |||||
chr2:58156583
|
TTTTTG | T | 36 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0106others(33): Show | 36 | HG00423.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1183-2736_1183-273 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156583 | |||||
chr2:58156583
|
TTTTTGTT others(3): Show |
T | 1 | a0002c0002t0002g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1183-2741_1183-273 others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156583 | |||||
chr2:58156585
|
TTTG | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183-2761_1183-275 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156585 | |||||
chr2:58156588
|
G | T | 16 | a0001c0001t0001g0145a0001c0003t0001g0007a0001c0003t0001g0008others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-2761G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156588 | ||||||
chr2:58156609
|
TTTTG | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-2736_1183-273 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156609 | |||||
chr2:58156613
|
G | GT | 9 | a0001c0001t0001g0145a0001c0003t0001g0264a0001c0003t0001g0266others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-2731dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156613 | |||||
chr2:58156685
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(157): Show | 165 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1183-2664C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156685 | ||||||
chr2:58157073
|
A | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1183-2276A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157073 | ||||||
chr2:58157300
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1183-2049A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157300 | ||||||
chr2:58157647
|
T | C | 1 | a0002c0002t0002g0333 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1183-1702T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157647 | ||||||
chr2:58157692
|
A | G | 9 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-1657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157692 | ||||||
chr2:58157714
|
C | T | 1 | a0002c0002t0002g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1183-1635C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157714 | ||||||
chr2:58157947
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0003c0005t0001g0114others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-1402T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157947 | ||||||
chr2:58158092
|
A | G | 24 | a0001c0001t0001g0262a0001c0001t0001g0313a0001c0001t0001g0314others(21): Show | 24 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-1257A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158092 | ||||||
chr2:58158108
|
T | G | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG01069.hp1 HG01256.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1183-1241T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158108 | ||||||
chr2:58158150
|
G | A | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1183-1199G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158150 | ||||||
chr2:58158170
|
T | TCTTA | 93 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0162others(90): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1183-1177_1183-117 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58158170 | |||||
chr2:58158182
|
T | C | 3 | a0001c0003t0004g0009a0001c0003t0004g0011a0001c0003t0004g0012 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1183-1167T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158182 | ||||||
chr2:58158187
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1183-1162T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158187 | ||||||
chr2:58158218
|
T | C | 260 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(257): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1183-1131T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158218 | ||||||
chr2:58158341
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1183-1008A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158341 | ||||||
chr2:58158375
|
C | G | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1183-974C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158375 | ||||||
chr2:58158544
|
T | TAA | 24 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-803_1183-802d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58158544 | |||||
chr2:58158651
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1183-698C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158651 | ||||||
chr2:58158717
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0331 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1183-632G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158717 | ||||||
chr2:58158780
|
C | A | 5 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-569C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158780 | ||||||
chr2:58158815
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1183-534C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158815 | ||||||
chr2:58159112
|
G | T | 117 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(114): Show | 118 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(115): Show |
intron_variant | MODIFIER | c.1183-237G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159112 | ||||||
chr2:58159183
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1183-166T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159183 | ||||||
chr2:58159201
|
T | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1183-148T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159201 |