geneid | 51755 |
---|---|
ensemblid | ENSG00000167258.16 |
hgncid | 24224 |
symbol | CDK12 |
name | cyclin dependent kinase 12 |
refseq_nuc | NM_016507.4 |
refseq_prot | NP_057591.2 |
ensembl_nuc | ENST00000447079.6 |
ensembl_prot | ENSP00000398880.4 |
mane_status | MANE Select |
chr | chr17 |
start | 39461486 |
end | 39534544 |
strand | + |
ver | v1.2 |
region | chr17:39461486-39534544 |
region5000 | chr17:39456486-39539544 |
regionname0 | CDK12_chr17_39461486_39534544 |
regionname5000 | CDK12_chr17_39456486_39539544 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1490 | 249 | 70 | 56 | 85 | 14 | 22 | 51 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0002 | 0/0 | 1490 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0003 | 0/0 | 1490 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0004 | 0/0 | 1490 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0005 | 0/0 | 1490 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0006 | 0/0 | 1490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0007 | 0/0 | 1490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0008 | 0/0 | 1490 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4473 | 234 | 56 | 56 | 85 | 14 | 21 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0002 | 0/0 | 4473 | 14 | 13 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0003 | 0/0 | 4473 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0004 | 0/0 | 4473 | 2 | 0 | 1 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0005 | 0/0 | 4473 | 2 | 1 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0006 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0007 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0008 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0009 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
c0010 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3810 | 108 | 14 | 32 | 43 | 7 | 11 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0002 | 1/0 | 3815 | 21 | 7 | 2 | 6 | 3 | 2 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0003 | 0/0 | 3813 | 18 | 3 | 6 | 9 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0004 | 0/0 | 3819 | 8 | 6 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0005 | 0/0 | 3817 | 8 | 2 | 1 | 4 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0006 | 0/0 | 3812 | 7 | 2 | 1 | 2 | 0 | 2 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0007 | 0/0 | 3811 | 6 | 3 | 1 | 1 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0008 | 0/0 | 3809 | 4 | 1 | 0 | 3 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0009 | 0/0 | 3834 | 4 | 4 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0010 | 0/0 | 3838 | 3 | 2 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0011 | 0/0 | 3834 | 3 | 0 | 3 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0012 | 0/0 | 3830 | 3 | 0 | 1 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0013 | 0/0 | 3828 | 3 | 1 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0014 | 0/0 | 3816 | 3 | 1 | 2 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0015 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0016 | 0/0 | 3810 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0017 | 0/0 | 3808 | 3 | 0 | 1 | 0 | 0 | 2 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0018 | 0/0 | 3842 | 2 | 1 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0019 | 0/0 | 3835 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0020 | 0/0 | 3833 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0021 | 0/0 | 3815 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0022 | 0/0 | 3814 | 2 | 1 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0023 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0024 | 0/0 | 3810 | 2 | 0 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0025 | 0/0 | 3807 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0026 | 0/0 | 3796 | 2 | 0 | 2 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0027 | 0/0 | 3811 | 2 | 0 | 1 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0028 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0029 | 0/0 | 3815 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0030 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0031 | 0/0 | 3816 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0032 | 0/0 | 3830 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0033 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0034 | 0/0 | 3850 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0035 | 0/0 | 3848 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0036 | 0/0 | 3844 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0037 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0038 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0039 | 0/0 | 3830 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0040 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0041 | 0/0 | 3827 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0042 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0043 | 0/0 | 3815 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0044 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0045 | 0/0 | 3810 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0046 | 0/0 | 3810 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0047 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0048 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0049 | 0/0 | 3809 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0050 | 0/0 | 3804 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0051 | 0/0 | 3802 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0052 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0053 | 0/0 | 3810 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0054 | 0/0 | 3809 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0055 | 0/0 | 3807 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0056 | 0/0 | 3815 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0057 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0058 | 0/0 | 3815 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
t0059 | 0/0 | 3815 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4473 | 234 | 56 | 56 | 85 | 14 | 21 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002 | 0/0 | 4473 | 14 | 13 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0007 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0002c0003 | 0/0 | 4473 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0003c0005 | 0/0 | 4473 | 2 | 1 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0004c0004 | 0/0 | 4473 | 2 | 0 | 1 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0005c0010 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0006c0008 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0007c0006 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0008c0009 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8282 | 106 | 14 | 32 | 42 | 7 | 10 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0002 | 1/0 | 8287 | 21 | 7 | 2 | 6 | 3 | 2 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0003 | 0/0 | 8285 | 18 | 3 | 6 | 9 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0004 | 0/0 | 8291 | 8 | 6 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0005 | 0/0 | 8289 | 8 | 2 | 1 | 4 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0006 | 0/0 | 8284 | 7 | 2 | 1 | 2 | 0 | 2 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0007 | 0/0 | 8283 | 6 | 3 | 1 | 1 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0008 | 0/0 | 8281 | 4 | 1 | 0 | 3 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0009 | 0/0 | 8306 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0010 | 0/0 | 8310 | 3 | 2 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0011 | 0/0 | 8306 | 3 | 0 | 3 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0012 | 0/0 | 8302 | 3 | 0 | 1 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0013 | 0/0 | 8300 | 3 | 1 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0014 | 0/0 | 8288 | 3 | 1 | 2 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0015 | 0/0 | 8286 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0017 | 0/0 | 8280 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0018 | 0/0 | 8314 | 2 | 1 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0022 | 0/0 | 8286 | 2 | 1 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0024 | 0/0 | 8282 | 2 | 0 | 0 | 2 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0026 | 0/0 | 8268 | 2 | 0 | 2 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0027 | 0/0 | 8283 | 2 | 0 | 1 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0028 | 0/0 | 8289 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0029 | 0/0 | 8287 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0030 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0031 | 0/0 | 8288 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0032 | 0/0 | 8302 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0033 | 0/0 | 8324 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0034 | 0/0 | 8322 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0036 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0037 | 0/0 | 8310 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0038 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0039 | 0/0 | 8302 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0040 | 0/0 | 8301 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0044 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0045 | 0/0 | 8282 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0046 | 0/0 | 8282 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0047 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0048 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0050 | 0/0 | 8276 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0051 | 0/0 | 8274 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0052 | 0/0 | 8306 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0053 | 0/0 | 8282 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0056 | 0/0 | 8287 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0057 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0001t0058 | 0/0 | 8287 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0019 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0020 | 0/0 | 8305 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0021 | 0/0 | 8287 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0023 | 0/0 | 8285 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0025 | 0/0 | 8279 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0041 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0042 | 0/0 | 8288 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0043 | 0/0 | 8287 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0049 | 0/0 | 8281 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0002t0059 | 0/0 | 8287 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0001c0007t0009 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0002c0003t0016 | 0/0 | 8282 | 3 | 3 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0003c0005t0054 | 0/0 | 8281 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0003c0005t0055 | 0/0 | 8279 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0004c0004t0017 | 0/0 | 8280 | 2 | 0 | 1 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0005c0010t0001 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0006c0008t0035 | 0/0 | 8320 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0007c0006t0019 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
a0008c0009t0001 | 0/0 | 8282 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | copy fasta | chr17 | 39456486 | 39539544 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0011g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0014g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0014g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0017g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0022g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0024g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0024g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0026g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0026g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0027g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0027g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0028g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0029g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0030g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0031g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0032g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0033g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0034g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0036g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0037g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0038g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0039g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0040g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0044g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0045g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0046g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0047g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0048g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0050g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0051g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0052g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0053g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0056g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0057g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0001t0058g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0019g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0020g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0021g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0021g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0023g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0023g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0025g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0025g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0041g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0042g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0043g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0049g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0002t0059g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0001c0007t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0002c0003t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0002c0003t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0002c0003t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0003c0005t0054g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0003c0005t0055g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0004c0004t0017g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0004c0004t0017g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0005c0010t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0006c0008t0035g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0007c0006t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
a0008c0009t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0022 | g0162 | EUR | GBR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00140 | hp1 | a0001 | c0001 | t0027 | g0048 | EUR | GBR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00597 | hp1 | a0001 | c0001 | t0058 | g0071 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01070 | hp1 | a0001 | c0001 | t0011 | g0104 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0103 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01074 | hp1 | a0001 | c0001 | t0027 | g0029 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01106 | hp2 | a0001 | c0001 | t0053 | g0134 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01109 | hp1 | a0003 | c0005 | t0055 | g0251 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01109 | hp2 | a0001 | c0001 | t0029 | g0025 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01192 | hp1 | a0001 | c0001 | t0056 | g0067 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01192 | hp2 | a0004 | c0004 | t0017 | g0161 | AMR | PUR | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01255 | hp2 | a0001 | c0001 | t0014 | g0159 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01257 | hp1 | a0001 | c0001 | t0011 | g0105 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01361 | hp2 | a0001 | c0001 | t0012 | g0093 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01433 | hp2 | a0001 | c0001 | t0026 | g0148 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0255 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01981 | hp1 | a0001 | c0001 | t0031 | g0247 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01981 | hp2 | a0001 | c0001 | t0026 | g0163 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02004 | hp1 | a0001 | c0001 | t0014 | g0130 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02055 | hp2 | a0002 | c0003 | t0016 | g0118 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02083 | hp1 | a0001 | c0001 | t0024 | g0227 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02129 | hp2 | a0001 | c0001 | t0040 | g0114 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02132 | hp1 | a0001 | c0001 | t0012 | g0115 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02145 | hp1 | a0002 | c0003 | t0016 | g0117 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0101 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | CDX | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | CDX | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0099 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02280 | hp1 | a0001 | c0001 | t0039 | g0102 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02280 | hp2 | a0001 | c0001 | t0037 | g0090 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02451 | hp1 | a0001 | c0002 | t0019 | g0009 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02602 | hp1 | a0001 | c0001 | t0048 | g0189 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02622 | hp1 | a0001 | c0002 | t0025 | g0259 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02630 | hp1 | a0001 | c0002 | t0025 | g0258 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02630 | hp2 | a0003 | c0005 | t0054 | g0252 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0191 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02717 | hp1 | a0007 | c0006 | t0019 | g0007 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02717 | hp2 | a0001 | c0001 | t0030 | g0073 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02738 | hp2 | a0001 | c0001 | t0018 | g0094 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02809 | hp2 | a0001 | c0001 | t0036 | g0092 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02886 | hp2 | a0001 | c0002 | t0020 | g0008 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02922 | hp1 | a0001 | c0002 | t0041 | g0010 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0109 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0182 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02970 | hp1 | a0001 | c0001 | t0034 | g0097 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0106 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03017 | hp1 | a0005 | c0010 | t0001 | g0179 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0108 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03098 | hp2 | a0001 | c0007 | t0009 | g0098 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03130 | hp1 | a0001 | c0002 | t0049 | g0004 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03139 | hp2 | a0006 | c0008 | t0035 | g0085 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0088 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03209 | hp2 | a0001 | c0002 | t0020 | g0011 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03225 | hp1 | a0001 | c0002 | t0021 | g0005 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03239 | hp1 | a0001 | c0001 | t0057 | g0176 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0107 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03486 | hp2 | a0001 | c0001 | t0018 | g0086 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0077 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03540 | hp1 | a0001 | c0002 | t0042 | g0020 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03579 | hp2 | a0001 | c0002 | t0023 | g0256 | AFR | MSL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03704 | hp1 | a0001 | c0001 | t0017 | g0207 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03704 | hp2 | a0004 | c0004 | t0017 | g0246 | SAS | PJL | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03834 | hp1 | a0001 | c0001 | t0047 | g0165 | SAS | BEB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0190 | SAS | BEB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG04204 | hp2 | a0001 | c0002 | t0059 | g0012 | SAS | STU | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18522 | hp2 | a0001 | c0002 | t0023 | g0257 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18906 | hp2 | a0001 | c0002 | t0043 | g0006 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18939 | hp1 | a0001 | c0001 | t0044 | g0199 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18940 | hp2 | a0001 | c0001 | t0028 | g0022 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18959 | hp2 | a0001 | c0001 | t0052 | g0111 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18961 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18975 | hp1 | a0001 | c0001 | t0051 | g0187 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18975 | hp2 | a0001 | c0001 | t0010 | g0091 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18984 | hp1 | a0001 | c0001 | t0013 | g0110 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18984 | hp2 | a0001 | c0001 | t0045 | g0231 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0041 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19001 | hp1 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19002 | hp2 | a0008 | c0009 | t0001 | g0167 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19005 | hp2 | a0001 | c0001 | t0024 | g0254 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19007 | hp1 | a0001 | c0001 | t0032 | g0113 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19009 | hp2 | a0001 | c0001 | t0013 | g0112 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19067 | hp2 | a0001 | c0001 | t0012 | g0095 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19086 | hp2 | a0001 | c0001 | t0046 | g0180 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19240 | hp1 | a0001 | c0001 | t0038 | g0089 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20752 | hp1 | a0001 | c0001 | t0033 | g0096 | EUR | TSI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0084 | EUR | TSI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20905 | hp1 | a0001 | c0001 | t0050 | g0150 | SAS | GIH | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | GIH | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02486 | hp2 | a0002 | c0003 | t0016 | g0119 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02559 | hp1 | a0001 | c0002 | t0021 | g0021 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0040 | REF | REF | CDK12_chr17_39456486_39539544 | CDK12 | chr17 | 39456486 | 39539544 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:39471421
|
C | T | 1 | a0005 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1589C>T | p.Pro530Leu | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/14 | 2175/8287 | 1589/4473 | 530/1490 | chr17 | 39471421 | ||
chr17:39494614
|
A | G | 1 | a0008 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.2339A>G | p.Gln780Arg | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/14 | 2925/8287 | 2339/4473 | 780/1490 | chr17 | 39494614 | ||
chr17:39526122
|
T | A | 1 | a0002 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.3566T>A | p.Leu1189Gln | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/14 | 4152/8287 | 3566/4473 | 1189/1490 | chr17 | 39526122 | ||
chr17:39526140
|
C | T | 1 | a0003 | 2 | HG01109.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.3584C>T | p.Thr1195Met | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/14 | 4170/8287 | 3584/4473 | 1195/1490 | chr17 | 39526140 | ||
chr17:39530667
|
C | T | 1 | a0004 | 2 | HG01192.hp2 HG03704.hp2 |
missense_variant | MODERATE | c.3824C>T | p.Pro1275Leu | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 4410/8287 | 3824/4473 | 1275/1490 | chr17 | 39530667 | ||
chr17:39530925
|
C | T | 1 | a0007 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.4082C>T | p.Ala1361Val | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 4668/8287 | 4082/4473 | 1361/1490 | chr17 | 39530925 | ||
chr17:39531258
|
A | G | 1 | a0006 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.4415A>G | p.Tyr1472Cys | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 5001/8287 | 4415/4473 | 1472/1490 | chr17 | 39531258 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:39462785
|
G | A | 2 | a0001c0002a0007c0006 | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
synonymous_variant | LOW | c.714G>A | p.Ser238Ser | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/14 | 1300/8287 | 714/4473 | 238/1490 | chr17 | 39462785 | ||
chr17:39471080
|
T | C | 1 | a0001c0007 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1248T>C | p.Asp416Asp | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/14 | 1834/8287 | 1248/4473 | 416/1490 | chr17 | 39471080 | ||
chr17:39526039
|
G | A | 2 | a0001c0002a0007c0006 | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
synonymous_variant | LOW | c.3483G>A | p.Thr1161Thr | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/14 | 4069/8287 | 3483/4473 | 1161/1490 | chr17 | 39526039 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:39461536
|
A | G | 1 | a0001c0002t0059 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-536A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/14 | 536 | chr17 | 39461536 | |||||
chr17:39461703
|
C | T | 1 | a0001c0001t0058 | 1 | HG00597.hp1 | 5_prime_UTR_variant | MODIFIER | c.-369C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/14 | 369 | chr17 | 39461703 | |||||
chr17:39461869
|
C | T | 1 | a0001c0001t0057 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/14 | 203 | chr17 | 39461869 | |||||
chr17:39461967
|
C | T | 2 | a0001c0001t0027a0001c0001t0056 | 3 | HG00140.hp1 HG01074.hp1 HG01192.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-105C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/14 | chr17 | 39461967 | ||||||
chr17:39531372
|
T | C | 1 | a0001c0001t0028 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 56 | chr17 | 39531372 | |||||
chr17:39531483
|
C | G | 2 | a0003c0005t0054a0003c0005t0055 | 2 | HG01109.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 167 | chr17 | 39531483 | |||||
chr17:39531676
|
A | G | 1 | a0001c0001t0053 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 360 | chr17 | 39531676 | |||||
chr17:39531715
|
A | G | 52 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(49): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 399 | chr17 | 39531715 | |||||
chr17:39532102
|
T | C | 1 | a0001c0001t0031 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*786T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 786 | chr17 | 39532102 | |||||
chr17:39532102
|
T | TTC | 2 | a0001c0001t0005a0001c0001t0028 | 9 | HG01496.hp1 HG01891.hp2 HG02015.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*827dupCT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 828 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTC | 1 | a0001c0001t0004 | 8 | HG02109.hp2 HG02895.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*827dupCTCT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 828 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(9): Show |
1 | a0001c0001t0032 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797_*798insATCTCT others(10): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 798 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(7): Show |
2 | a0001c0001t0013a0001c0001t0040 | 4 | HG02129.hp2 HG02922.hp2 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(9): Show |
2 | a0001c0001t0012a0001c0001t0039 | 4 | HG01361.hp2 HG02132.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(10): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(13): Show |
3 | a0001c0001t0009a0001c0001t0011a0001c0007t0009 | 7 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(15): Show |
1 | a0001c0001t0038 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(17): Show |
2 | a0001c0001t0010a0001c0001t0037 | 4 | HG02280.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(21): Show |
1 | a0001c0001t0018 | 2 | HG02738.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(22): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(23): Show |
1 | a0001c0001t0036 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(24): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(27): Show |
1 | a0006c0008t0035 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(28): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(29): Show |
1 | a0001c0001t0034 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(30): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
T | TTCTCTCT others(31): Show |
1 | a0001c0001t0033 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799_*800insATCTCT others(32): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 800 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTC | T | 3 | a0001c0001t0003a0001c0001t0022a0001c0002t0023 | 22 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*827delCT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 826 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTCTC | T | 4 | a0001c0001t0006a0001c0001t0007a0001c0001t0027others(1): Show | 16 | HG00140.hp1 HG01074.hp1 HG01255.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*827delCTCT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 824 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTCTCTC | T | 14 | a0001c0001t0001a0001c0001t0008a0001c0001t0024others(11): Show | 125 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*822_*827delCTCTCT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 822 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTCTCTCT others(1): Show |
T | 5 | a0001c0001t0017a0001c0001t0030a0001c0002t0025others(2): Show | 7 | HG01109.hp1 HG01192.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*820_*827delCTCTCT others(2): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 820 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0050a0001c0001t0051 | 2 | NA18975.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*816_*827delCTCTCT others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 816 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532102
|
TTCTCTCT others(13): Show |
T | 1 | a0001c0001t0026 | 2 | HG01433.hp2 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*808_*827delCTCTCT others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 808 | INFO_REALIGN_3_PRIME | chr17 | 39532102 | ||||
chr17:39532106
|
C | CTCTCTTT others(13): Show |
1 | a0001c0001t0052 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*795_*796insTTCTCT others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 796 | INFO_REALIGN_3_PRIME | chr17 | 39532106 | ||||
chr17:39532140
|
C | CTCTCTCT others(13): Show |
2 | a0001c0002t0019a0007c0006t0019 | 2 | HG02451.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*827_*828insCTCTCT others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 828 | INFO_REALIGN_3_PRIME | chr17 | 39532140 | ||||
chr17:39532140
|
C | CTCTCTCT others(11): Show |
1 | a0001c0002t0020 | 2 | HG02886.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*827_*828insCTCTCT others(12): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 828 | INFO_REALIGN_3_PRIME | chr17 | 39532140 | ||||
chr17:39532140
|
C | CTCTCTCT others(5): Show |
1 | a0001c0002t0041 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827_*828insCTCTCT others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 828 | INFO_REALIGN_3_PRIME | chr17 | 39532140 | ||||
chr17:39532140
|
C | G | 46 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(43): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*824C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 824 | chr17 | 39532140 | |||||
chr17:39532157
|
G | A | 1 | a0001c0001t0024 | 2 | HG02083.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*841G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 841 | chr17 | 39532157 | |||||
chr17:39532326
|
G | T | 1 | a0002c0003t0016 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1010G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 1010 | chr17 | 39532326 | |||||
chr17:39532461
|
CA | C | 18 | a0001c0001t0009a0001c0001t0010a0001c0001t0011others(15): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1155delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 1155 | INFO_REALIGN_3_PRIME | chr17 | 39532461 | ||||
chr17:39532533
|
C | A | 1 | a0001c0001t0032 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1217C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 1217 | chr17 | 39532533 | |||||
chr17:39533074
|
T | TA | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(17): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1770dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 1771 | INFO_REALIGN_3_PRIME | chr17 | 39533074 | ||||
chr17:39533240
|
G | A | 1 | a0001c0001t0029 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 1924 | chr17 | 39533240 | |||||
chr17:39533316
|
T | C | 1 | a0001c0001t0039 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2000T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2000 | chr17 | 39533316 | |||||
chr17:39533373
|
C | G | 1 | a0001c0001t0048 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2057 | chr17 | 39533373 | |||||
chr17:39533519
|
T | G | 9 | a0001c0001t0009a0001c0001t0018a0001c0001t0033others(6): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2203T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2203 | chr17 | 39533519 | |||||
chr17:39533681
|
G | A | 1 | a0001c0001t0045 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2365G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2365 | chr17 | 39533681 | |||||
chr17:39534014
|
C | T | 1 | a0001c0001t0047 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2698C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2698 | chr17 | 39534014 | |||||
chr17:39534116
|
C | T | 1 | a0001c0001t0052 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2800 | chr17 | 39534116 | |||||
chr17:39534257
|
C | T | 1 | a0001c0001t0046 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2941C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 14/14 | 2941 | chr17 | 39534257 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:39463557
|
A | G | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+440A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39463557 | ||||||
chr17:39463800
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1046+683C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39463800 | ||||||
chr17:39464094
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1046+977A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464094 | ||||||
chr17:39464110
|
A | G | 1 | a0001c0001t0004g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1046+993A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464110 | ||||||
chr17:39464143
|
A | G | 1 | a0001c0001t0024g0254 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1046+1026A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464143 | ||||||
chr17:39464374
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1046+1257C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464374 | ||||||
chr17:39464379
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1046+1262C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464379 | ||||||
chr17:39464404
|
C | CT | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1046+1299dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39464404 | |||||
chr17:39464404
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1046+1299delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39464404 | |||||
chr17:39464686
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG00738.hp2 HG01934.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+1569C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464686 | ||||||
chr17:39464705
|
A | C | 1 | a0004c0004t0017g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1046+1588A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464705 | ||||||
chr17:39464749
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1046+1632A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464749 | ||||||
chr17:39464789
|
GA | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1046+1685delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39464789 | |||||
chr17:39464800
|
A | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1046+1683A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464800 | ||||||
chr17:39464814
|
C | T | 6 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG00741.hp1 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1046+1697C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464814 | ||||||
chr17:39464869
|
T | C | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1046+1752T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464869 | ||||||
chr17:39464925
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1046+1808C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39464925 | ||||||
chr17:39464951
|
C | CA | 20 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(17): Show | 20 | HG01071.hp1 HG01256.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046+1848dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39464951 | |||||
chr17:39465114
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1046+1997C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465114 | ||||||
chr17:39465119
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1046+2002G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465119 | ||||||
chr17:39465162
|
G | T | 1 | a0001c0001t0004g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1046+2045G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465162 | ||||||
chr17:39465200
|
C | T | 1 | a0001c0001t0010g0091 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1046+2083C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465200 | ||||||
chr17:39465251
|
T | TA | 158 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1046+2152dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39465251 | |||||
chr17:39465251
|
T | TAA | 19 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(16): Show | 19 | HG00741.hp2 HG01106.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1046+2151_1046+215 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39465251 | |||||
chr17:39465353
|
A | G | 1 | a0001c0001t0012g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1046+2236A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465353 | ||||||
chr17:39465401
|
CT | C | 16 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(13): Show | 16 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+2297delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39465401 | |||||
chr17:39465401
|
CTT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1046+2296_1046+229 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39465401 | |||||
chr17:39465677
|
G | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1046+2560G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465677 | ||||||
chr17:39465749
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1046+2632C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39465749 | ||||||
chr17:39466033
|
G | A | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1046+2916G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466033 | ||||||
chr17:39466136
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02015.hp2 HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1046+3019C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466136 | ||||||
chr17:39466169
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1046+3052G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466169 | ||||||
chr17:39466200
|
CGGGAGGC others(299): Show |
C | 1 | a0001c0001t0012g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1046+3105_1046+341 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466200 | |||||
chr17:39466264
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1046+3147C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466264 | ||||||
chr17:39466307
|
C | CA | 23 | a0001c0001t0001g0140a0001c0001t0009g0087a0001c0001t0009g0088others(20): Show | 23 | HG02055.hp1 HG02080.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1046+3205dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466307 | |||||
chr17:39466307
|
CA | C | 6 | a0001c0001t0001g0138a0001c0001t0002g0076a0001c0001t0003g0078others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1046+3205delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466307 | |||||
chr17:39466421
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1046+3304C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466421 | ||||||
chr17:39466472
|
G | C | 27 | a0001c0001t0001g0120a0001c0001t0001g0133a0001c0001t0001g0140others(24): Show | 27 | HG00438.hp2 HG01106.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1046+3355G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466472 | ||||||
chr17:39466541
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1046+3424G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466541 | ||||||
chr17:39466561
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1046+3444C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466561 | ||||||
chr17:39466615
|
G | GA | 9 | a0001c0001t0001g0027a0001c0001t0002g0028a0001c0001t0002g0034others(6): Show | 9 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1046+3538dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
G | GAA | 8 | a0001c0001t0002g0026a0001c0001t0004g0016a0001c0001t0004g0017others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1046+3537_1046+353 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
G | GAAA | 5 | a0001c0001t0004g0013a0001c0001t0004g0014a0001c0001t0005g0015others(2): Show | 5 | HG02109.hp2 HG03041.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+3536_1046+353 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GA | G | 14 | a0001c0001t0001g0164a0001c0001t0002g0066a0001c0001t0002g0083others(11): Show | 14 | HG00597.hp1 HG00673.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1046+3538delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAA | G | 5 | a0001c0001t0001g0166a0001c0001t0006g0253a0001c0001t0047g0165others(2): Show | 5 | HG01106.hp2 HG01255.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+3535_1046+353 others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAA | G | 18 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG00621.hp1 HG01361.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1046+3534_1046+353 others(9): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAA | G | 47 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1046+3533_1046+353 others(10): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0129others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1046+3532_1046+353 others(11): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(1): Show |
G | 7 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 7 | HG02486.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046+3531_1046+353 others(12): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(3): Show |
G | 5 | a0001c0002t0021g0005a0001c0002t0023g0256a0001c0002t0043g0006others(2): Show | 5 | HG03130.hp1 HG03225.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+3529_1046+353 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(4): Show |
G | 4 | a0001c0001t0007g0084a0001c0002t0023g0257a0003c0005t0055g0251others(1): Show | 4 | HG01109.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+3528_1046+353 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(5): Show |
G | 3 | a0001c0002t0025g0258a0001c0002t0025g0259a0003c0005t0054g0252 | 3 | HG02622.hp1 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1046+3527_1046+353 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(8): Show |
G | 1 | a0001c0002t0021g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1046+3524_1046+353 others(19): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(9): Show |
G | 2 | a0004c0004t0017g0161a0004c0004t0017g0246 | 2 | HG01192.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1046+3523_1046+353 others(20): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1046+3522_1046+353 others(21): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(11): Show |
G | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+3521_1046+353 others(22): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(12): Show |
G | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1046+3520_1046+353 others(23): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(13): Show |
G | 2 | a0001c0001t0012g0095a0001c0001t0018g0094 | 2 | HG02738.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1046+3519_1046+353 others(24): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(14): Show |
G | 20 | a0001c0001t0002g0076a0001c0001t0003g0078a0001c0001t0007g0075others(17): Show | 20 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1046+3518_1046+353 others(25): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466615
|
GAAAAAAA others(15): Show |
G | 14 | a0001c0001t0002g0019a0001c0001t0009g0108a0001c0001t0010g0091others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1046+3517_1046+353 others(26): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466615 | |||||
chr17:39466621
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1046+3504A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466621 | ||||||
chr17:39466623
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1046+3506A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466623 | ||||||
chr17:39466735
|
G | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG00738.hp2 HG01934.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+3618G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466735 | ||||||
chr17:39466776
|
C | T | 3 | a0001c0002t0021g0005a0001c0002t0043g0006a0001c0002t0049g0004 | 3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1046+3659C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466776 | ||||||
chr17:39466878
|
G | T | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1046+3761G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466878 | ||||||
chr17:39466919
|
CT | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1046+3804delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39466919 | |||||
chr17:39466956
|
T | G | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+3839T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39466956 | ||||||
chr17:39467088
|
C | T | 4 | a0001c0001t0002g0080a0001c0001t0002g0082a0001c0001t0002g0083others(1): Show | 4 | HG00741.hp1 HG01515.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-3791C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467088 | ||||||
chr17:39467112
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1047-3767G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467112 | ||||||
chr17:39467135
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1047-3744T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467135 | ||||||
chr17:39467213
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1047-3666A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467213 | ||||||
chr17:39467275
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-3604C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467275 | ||||||
chr17:39467475
|
C | T | 1 | a0001c0001t0058g0071 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1047-3404C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467475 | ||||||
chr17:39467490
|
A | G | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1047-3389A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39467490 | ||||||
chr17:39468125
|
A | ACT | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1047-2754_1047-275 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468125 | ||||||
chr17:39468186
|
C | T | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1047-2693C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468186 | ||||||
chr17:39468537
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1047-2342A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468537 | ||||||
chr17:39468578
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0035 | 2 | HG01256.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1047-2301C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468578 | ||||||
chr17:39468658
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1047-2221A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468658 | ||||||
chr17:39468729
|
C | T | 6 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0018g0086others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047-2150C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468729 | ||||||
chr17:39468806
|
A | T | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135others(15): Show | 18 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1047-2073A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468806 | ||||||
chr17:39468810
|
T | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(138): Show | 142 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1047-2069T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468810 | ||||||
chr17:39468814
|
T | A | 68 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(65): Show | 68 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1047-2065T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468814 | ||||||
chr17:39468818
|
T | A | 15 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(12): Show | 15 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-2061T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468818 | ||||||
chr17:39468822
|
T | A | 2 | a0001c0001t0001g0138a0001c0001t0006g0139 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1047-2057T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468822 | ||||||
chr17:39468931
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1047-1948T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468931 | ||||||
chr17:39468988
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1047-1891C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39468988 | ||||||
chr17:39469456
|
G | A | 2 | a0001c0001t0014g0141a0001c0001t0022g0182 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1047-1423G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469456 | ||||||
chr17:39469488
|
A | G | 1 | a0001c0001t0050g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1047-1391A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469488 | ||||||
chr17:39469636
|
C | CT | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1047-1225dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39469636 | |||||
chr17:39469636
|
CT | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0131a0001c0001t0001g0211others(7): Show | 10 | HG01069.hp1 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1047-1225delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39469636 | |||||
chr17:39469659
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1047-1220C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469659 | ||||||
chr17:39469778
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1047-1101C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469778 | ||||||
chr17:39469904
|
T | C | 5 | a0001c0001t0004g0030a0001c0001t0005g0023a0001c0001t0005g0024others(2): Show | 5 | HG01496.hp1 NA18940.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-975T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469904 | ||||||
chr17:39469906
|
G | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1047-973G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39469906 | ||||||
chr17:39470065
|
T | G | 1 | a0001c0001t0007g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1047-814T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470065 | ||||||
chr17:39470134
|
T | C | 1 | a0001c0001t0007g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1047-745T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470134 | ||||||
chr17:39470135
|
A | AT | 13 | a0001c0001t0003g0070a0001c0001t0010g0091a0001c0001t0011g0103others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1047-730dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 39470135 | |||||
chr17:39470263
|
G | C | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-616G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470263 | ||||||
chr17:39470322
|
C | T | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1047-557C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470322 | ||||||
chr17:39470363
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1047-516T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470363 | ||||||
chr17:39470365
|
C | T | 1 | a0001c0001t0007g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1047-514C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470365 | ||||||
chr17:39470367
|
C | T | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047-512C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470367 | ||||||
chr17:39470410
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1047-469C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470410 | ||||||
chr17:39470710
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1047-169G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470710 | ||||||
chr17:39470768
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1047-111T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 1/13 | chr17 | 39470768 | ||||||
chr17:39471919
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1931+156G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39471919 | ||||||
chr17:39471965
|
T | G | 1 | a0001c0002t0025g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1931+202T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39471965 | ||||||
chr17:39472321
|
A | T | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1931+558A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472321 | ||||||
chr17:39472406
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1931+643A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472406 | ||||||
chr17:39472507
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+744C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472507 | ||||||
chr17:39472527
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1931+764A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472527 | ||||||
chr17:39472611
|
T | C | 2 | a0001c0001t0014g0141a0001c0001t0022g0182 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1931+848T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472611 | ||||||
chr17:39472641
|
A | G | 2 | a0001c0001t0022g0162a0001c0001t0026g0163 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1931+878A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472641 | ||||||
chr17:39472721
|
C | G | 2 | a0001c0001t0002g0059a0001c0001t0003g0060 | 2 | NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1931+958C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472721 | ||||||
chr17:39472735
|
C | T | 2 | a0001c0001t0006g0190a0001c0001t0006g0191 | 2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1931+972C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472735 | ||||||
chr17:39472737
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1931+974C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472737 | ||||||
chr17:39472795
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1931+1032G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472795 | ||||||
chr17:39472799
|
G | C | 1 | a0001c0001t0024g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1931+1036G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39472799 | ||||||
chr17:39472889
|
CA | C | 11 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1931+1128delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39472889 | |||||
chr17:39473070
|
C | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1931+1307C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473070 | ||||||
chr17:39473075
|
T | TA | 7 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(4): Show | 7 | HG00621.hp1 HG01106.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.1931+1325dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39473075 | |||||
chr17:39473187
|
C | G | 2 | a0001c0001t0022g0162a0001c0001t0026g0163 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1931+1424C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473187 | ||||||
chr17:39473231
|
C | T | 3 | a0001c0002t0021g0005a0001c0002t0043g0006a0001c0002t0049g0004 | 3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1468C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473231 | ||||||
chr17:39473232
|
A | T | 3 | a0001c0002t0021g0005a0001c0002t0043g0006a0001c0002t0049g0004 | 3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1469A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473232 | ||||||
chr17:39473245
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0183 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1931+1482G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473245 | ||||||
chr17:39473433
|
A | G | 1 | a0001c0007t0009g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1931+1670A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473433 | ||||||
chr17:39473480
|
G | A | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1931+1717G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473480 | ||||||
chr17:39473538
|
T | C | 11 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1931+1775T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473538 | ||||||
chr17:39473596
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1931+1833A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473596 | ||||||
chr17:39473756
|
T | G | 2 | a0001c0001t0022g0162a0001c0001t0026g0163 | 2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1931+1993T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473756 | ||||||
chr17:39473918
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0006g0232 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1931+2155G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473918 | ||||||
chr17:39473989
|
A | G | 1 | a0003c0005t0054g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1931+2226A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39473989 | ||||||
chr17:39474188
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1931+2425T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474188 | ||||||
chr17:39474648
|
C | T | 1 | a0001c0001t0032g0113 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1931+2885C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474648 | ||||||
chr17:39474772
|
T | A | 1 | a0001c0001t0003g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1931+3009T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474772 | ||||||
chr17:39474781
|
C | CT | 32 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0145others(29): Show | 32 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1931+3040dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39474781 | |||||
chr17:39474781
|
C | CTT | 7 | a0001c0001t0010g0091a0001c0001t0012g0095a0001c0001t0012g0115others(4): Show | 7 | HG02132.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1931+3039_1931+304 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39474781 | |||||
chr17:39474781
|
C | CTTT | 7 | a0001c0002t0019g0009a0001c0002t0020g0011a0001c0002t0021g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1931+3038_1931+304 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39474781 | |||||
chr17:39474781
|
CT | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0184others(13): Show | 16 | HG02004.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1931+3040delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39474781 | |||||
chr17:39474842
|
A | T | 5 | a0001c0001t0002g0018a0001c0001t0004g0014a0001c0001t0004g0016others(2): Show | 5 | HG02895.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1931+3079A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474842 | ||||||
chr17:39474888
|
C | T | 1 | a0001c0001t0007g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1931+3125C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474888 | ||||||
chr17:39474890
|
A | G | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1931+3127A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39474890 | ||||||
chr17:39475547
|
A | AT | 9 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0234others(6): Show | 9 | HG02523.hp1 HG02602.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1931+3802dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39475547 | |||||
chr17:39475548
|
T | A | 1 | a0001c0002t0049g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1931+3785T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475548 | ||||||
chr17:39475591
|
G | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1931+3828G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475591 | ||||||
chr17:39475630
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+3867C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475630 | ||||||
chr17:39475646
|
G | C | 1 | a0001c0001t0002g0059 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1931+3883G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475646 | ||||||
chr17:39475671
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+3908G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475671 | ||||||
chr17:39475835
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1931+4072A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475835 | ||||||
chr17:39475837
|
G | A | 1 | a0001c0001t0034g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1931+4074G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475837 | ||||||
chr17:39475926
|
G | A | 3 | a0001c0001t0018g0086a0001c0001t0038g0089a0006c0008t0035g0085 | 3 | HG03139.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1931+4163G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39475926 | ||||||
chr17:39476111
|
T | G | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1931+4348T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476111 | ||||||
chr17:39476366
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1931+4603C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476366 | ||||||
chr17:39476423
|
T | G | 15 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG01106.hp1 HG01123.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1931+4660T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476423 | ||||||
chr17:39476457
|
G | T | 6 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0018g0086others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1931+4694G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476457 | ||||||
chr17:39476708
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1931+4945T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476708 | ||||||
chr17:39476711
|
C | CATTTTTT others(2): Show |
5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0022g0182others(2): Show | 5 | HG02004.hp2 HG02965.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1931+4948_1931+494 others(13): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CATTTTTT others(3): Show |
49 | a0001c0001t0001g0027a0001c0001t0001g0120a0001c0001t0001g0121others(46): Show | 49 | HG00140.hp2 HG00673.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1931+4948_1931+494 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CATTTTTT others(4): Show |
58 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0123others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1931+4948_1931+494 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CATTTTTT others(5): Show |
13 | a0001c0001t0001g0136a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 13 | HG00597.hp2 HG01106.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1931+4948_1931+494 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CATTTTTT others(7): Show |
2 | a0001c0001t0001g0234a0001c0001t0048g0189 | 2 | HG02602.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1931+4948_1931+494 others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CATTTTTT others(9): Show |
1 | a0001c0001t0001g0133 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1931+4948_1931+494 others(20): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476711 | ||||||
chr17:39476711
|
C | CT | 7 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0013g0112others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1931+4977dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTT | 6 | a0001c0001t0005g0032a0001c0001t0010g0091a0001c0001t0010g0106others(3): Show | 6 | HG02145.hp2 HG02738.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1931+4976_1931+497 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0076a0001c0001t0007g0072 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1931+4967_1931+497 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0003g0078a0001c0001t0007g0075a0001c0001t0008g0077 | 3 | HG02258.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1931+4966_1931+497 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1931+4964_1931+497 others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(8): Show |
7 | a0001c0001t0002g0036a0001c0001t0002g0043a0001c0001t0002g0044others(4): Show | 7 | HG01109.hp2 HG01515.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1931+4963_1931+497 others(19): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(9): Show |
10 | a0001c0001t0002g0034a0001c0001t0002g0082a0001c0001t0003g0047others(7): Show | 10 | HG00140.hp1 HG00673.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1931+4962_1931+497 others(20): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0002g0026a0001c0001t0002g0058a0001c0001t0002g0081others(3): Show | 6 | HG00423.hp1 HG00621.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1931+4961_1931+497 others(21): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0062others(1): Show | 4 | HG00738.hp1 HG01975.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1931+4960_1931+497 others(22): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0008g0054 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1931+4959_1931+497 others(23): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1931+4958_1931+497 others(24): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(15): Show |
8 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0005g0003others(5): Show | 8 | HG01074.hp1 HG01192.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1931+4956_1931+497 others(26): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0003g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1931+4954_1931+497 others(28): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(18): Show |
4 | a0001c0001t0003g0002a0001c0001t0003g0069a0001c0001t0004g0116others(1): Show | 4 | HG01943.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1931+4953_1931+497 others(29): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0002g0019a0001c0001t0003g0056a0001c0001t0004g0013 | 3 | HG02109.hp2 HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1931+4952_1931+497 others(30): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(20): Show |
3 | a0001c0001t0002g0038a0001c0001t0004g0014a0001c0001t0004g0030 | 3 | HG03209.hp1 HG03579.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1931+4951_1931+497 others(31): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0030g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1931+4950_1931+497 others(32): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(22): Show |
2 | a0001c0001t0002g0018a0001c0001t0003g0068 | 2 | NA18906.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1931+4949_1931+497 others(33): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0004g0017a0001c0001t0005g0024 | 2 | HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1931+4977_1931+497 others(34): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0007g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1931+4977_1931+497 others(37): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476711
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0046g0180 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1931+4968_1931+497 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476711 | |||||
chr17:39476713
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1931+4950T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476713 | ||||||
chr17:39476716
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1931+4953T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476716 | ||||||
chr17:39476716
|
T | TTTTTTTT others(2): Show |
7 | a0001c0002t0020g0008a0001c0002t0020g0011a0001c0002t0021g0005others(4): Show | 7 | HG02717.hp1 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1931+4961_1931+496 others(13): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476716 | |||||
chr17:39476716
|
T | TTTTTTTT others(3): Show |
4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931+4962_1931+496 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39476716 | |||||
chr17:39476717
|
T | A | 2 | a0001c0001t0001g0239a0001c0001t0006g0204 | 2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1931+4954T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476717 | ||||||
chr17:39476718
|
T | A | 3 | a0001c0001t0001g0240a0001c0001t0006g0190a0001c0001t0006g0191 | 3 | HG02015.hp2 HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1931+4955T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476718 | ||||||
chr17:39476722
|
T | A | 1 | a0001c0001t0046g0180 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1931+4959T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476722 | ||||||
chr17:39476762
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1931+4999G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476762 | ||||||
chr17:39476788
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1931+5025T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476788 | ||||||
chr17:39476791
|
C | T | 2 | a0001c0001t0014g0141a0001c0001t0022g0182 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1931+5028C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39476791 | ||||||
chr17:39477167
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1931+5404T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477167 | ||||||
chr17:39477341
|
T | C | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1931+5578T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477341 | ||||||
chr17:39477518
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1931+5755G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477518 | ||||||
chr17:39477522
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1931+5759G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477522 | ||||||
chr17:39477574
|
AT | A | 16 | a0001c0001t0002g0255a0001c0001t0004g0079a0001c0001t0008g0054others(13): Show | 16 | HG01516.hp1 HG02451.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1931+5827delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39477574 | |||||
chr17:39477578
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1931+5815T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477578 | ||||||
chr17:39477582
|
T | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1931+5819T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477582 | ||||||
chr17:39477611
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1931+5848C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477611 | ||||||
chr17:39477717
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1931+5954C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477717 | ||||||
chr17:39477808
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1931+6045C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477808 | ||||||
chr17:39477936
|
G | C | 1 | a0001c0001t0010g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1931+6173G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477936 | ||||||
chr17:39477983
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1931+6220G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39477983 | ||||||
chr17:39478063
|
CT | C | 16 | a0001c0001t0001g0171a0001c0001t0002g0028a0001c0002t0020g0008others(13): Show | 16 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1931+6315delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39478063 | |||||
chr17:39478200
|
A | AT | 140 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1931+6448dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39478200 | |||||
chr17:39478491
|
G | C | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1931+6728G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39478491 | ||||||
chr17:39478900
|
A | G | 1 | a0001c0001t0007g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1931+7137A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39478900 | ||||||
chr17:39479233
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0211 | 3 | HG01069.hp1 HG02109.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1931+7470G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479233 | ||||||
chr17:39479259
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1931+7496G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479259 | ||||||
chr17:39479290
|
AAG | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1931+7530_1931+753 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39479290 | |||||
chr17:39479308
|
G | GA | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1931+7566dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39479308 | |||||
chr17:39479308
|
G | GAA | 12 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0173others(9): Show | 12 | HG01934.hp2 HG01981.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1931+7565_1931+756 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39479308 | |||||
chr17:39479338
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1931+7575T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479338 | ||||||
chr17:39479397
|
A | C | 12 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0208others(9): Show | 12 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1931+7634A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479397 | ||||||
chr17:39479402
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1931+7639G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479402 | ||||||
chr17:39479511
|
G | A | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931+7748G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479511 | ||||||
chr17:39479924
|
CT | C | 111 | a0001c0001t0001g0212a0001c0001t0002g0018a0001c0001t0002g0019others(108): Show | 111 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1931+8177delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39479924 | |||||
chr17:39479924
|
CTT | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1931+8176_1931+817 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39479924 | |||||
chr17:39479992
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0183 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1931+8229C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39479992 | ||||||
chr17:39480046
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1931+8283C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480046 | ||||||
chr17:39480122
|
C | T | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1931+8359C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480122 | ||||||
chr17:39480264
|
C | CT | 14 | a0001c0001t0003g0031a0001c0001t0010g0091a0001c0001t0011g0103others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1931+8516dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39480264 | |||||
chr17:39480279
|
T | TC | 16 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135others(13): Show | 16 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1931+8518dupC | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39480279 | |||||
chr17:39480325
|
G | A | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1931+8562G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480325 | ||||||
chr17:39480330
|
C | T | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1931+8567C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480330 | ||||||
chr17:39480382
|
G | A | 9 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0004g0013others(6): Show | 9 | HG02109.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1931+8619G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480382 | ||||||
chr17:39480437
|
T | G | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931+8674T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480437 | ||||||
chr17:39480442
|
T | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+8679T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480442 | ||||||
chr17:39480469
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1931+8706G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480469 | ||||||
chr17:39480738
|
T | C | 1 | a0001c0001t0007g0046 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1931+8975T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480738 | ||||||
chr17:39480820
|
C | G | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1931+9057C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480820 | ||||||
chr17:39480947
|
C | G | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1931+9184C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480947 | ||||||
chr17:39480999
|
A | C | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1931+9236A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39480999 | ||||||
chr17:39481150
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+9387G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481150 | ||||||
chr17:39481242
|
AAACTCCG others(4): Show |
A | 1 | a0006c0008t0035g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1932-9312_1932-930 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481242 | |||||
chr17:39481265
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1932-9292G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481265 | ||||||
chr17:39481265
|
GA | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1932-9280delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481265 | |||||
chr17:39481266
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1932-9291A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481266 | ||||||
chr17:39481329
|
C | CT | 6 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0011g0105others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932-9212dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481329 | |||||
chr17:39481329
|
CT | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0200a0001c0001t0003g0031others(2): Show | 5 | HG02080.hp1 HG02080.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932-9212delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481329 | |||||
chr17:39481331
|
T | C | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1932-9226T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481331 | ||||||
chr17:39481387
|
G | A | 1 | a0001c0001t0026g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1932-9170G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481387 | ||||||
chr17:39481470
|
G | GT | 5 | a0001c0001t0002g0036a0001c0001t0003g0031a0001c0001t0003g0068others(2): Show | 5 | HG02738.hp1 HG03491.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1932-9076dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481470 | |||||
chr17:39481493
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0007g0084 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1932-9064A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481493 | ||||||
chr17:39481602
|
G | A | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1932-8955G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481602 | ||||||
chr17:39481617
|
GCTTGCTC others(17): Show |
G | 1 | a0001c0001t0008g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1932-8937_1932-891 others(28): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481617 | |||||
chr17:39481621
|
GCTCGCTC others(27): Show |
G | 1 | a0001c0001t0003g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1932-8932_1932-889 others(38): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481621 | |||||
chr17:39481625
|
GCTCGCGC others(15): Show |
G | 1 | a0001c0001t0002g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1932-8928_1932-890 others(26): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481625 | |||||
chr17:39481629
|
GCGCGCTC others(19): Show |
G | 1 | a0001c0001t0007g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1932-8926_1932-890 others(30): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481629 | |||||
chr17:39481631
|
G | GCCCTCTC others(15): Show |
1 | a0001c0001t0007g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1932-8925_1932-892 others(26): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481631 | |||||
chr17:39481631
|
GCGCTCTC others(5): Show |
G | 1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1932-8924_1932-891 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481631 | |||||
chr17:39481631
|
GCGCTCTC others(51): Show |
G | 4 | a0001c0001t0001g0142a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01255.hp1 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-8924_1932-886 others(62): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481631 | |||||
chr17:39481631
|
GCGCTCTC others(53): Show |
G | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1932-8924_1932-886 others(64): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481631 | |||||
chr17:39481631
|
GCGCTCTC others(57): Show |
G | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1932-8924_1932-886 others(68): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481631 | |||||
chr17:39481633
|
G | C | 2 | a0001c0001t0007g0074a0001c0001t0030g0073 | 2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1932-8924G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481633 | ||||||
chr17:39481633
|
G | GCT | 3 | a0001c0001t0002g0019a0001c0001t0005g0032a0001c0001t0007g0046 | 3 | HG02486.hp1 NA18961.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1932-8847_1932-884 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
G | GCTCTCTC others(3): Show |
1 | a0001c0001t0002g0026 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1932-8855_1932-884 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
G | T | 2 | a0001c0001t0004g0079a0001c0001t0007g0072 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-8924G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481633 | ||||||
chr17:39481633
|
GCT | G | 5 | a0001c0001t0002g0036a0001c0001t0003g0049a0001c0001t0004g0014others(2): Show | 5 | HG01074.hp1 HG03491.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932-8847_1932-884 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCT | G | 7 | a0001c0001t0002g0034a0001c0001t0002g0058a0001c0001t0002g0059others(4): Show | 7 | HG00621.hp2 HG00673.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1932-8849_1932-884 others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(1): Show |
G | 3 | a0001c0001t0003g0070a0001c0001t0004g0017a0001c0001t0029g0025 | 3 | HG01109.hp2 HG02976.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1932-8853_1932-884 others(12): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(3): Show |
G | 4 | a0001c0001t0003g0069a0001c0001t0004g0013a0001c0001t0004g0016others(1): Show | 4 | HG01943.hp1 HG02109.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-8855_1932-884 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(5): Show |
G | 6 | a0001c0001t0002g0043a0001c0001t0002g0066a0001c0001t0002g0080others(3): Show | 6 | HG00597.hp1 HG00738.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932-8857_1932-884 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(7): Show |
G | 2 | a0001c0001t0003g0002a0001c0001t0003g0050 | 2 | HG02040.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1932-8859_1932-884 others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(9): Show |
G | 5 | a0001c0001t0002g0038a0001c0001t0002g0042a0001c0001t0002g0081others(2): Show | 5 | HG01123.hp2 HG01515.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932-8861_1932-884 others(20): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(11): Show |
G | 3 | a0001c0001t0002g0018a0001c0001t0004g0116a0001c0001t0028g0022 | 3 | HG02895.hp1 NA18906.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1932-8863_1932-884 others(22): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(13): Show |
G | 1 | a0001c0001t0005g0023 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1932-8865_1932-884 others(24): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(15): Show |
G | 1 | a0001c0001t0056g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1932-8867_1932-884 others(26): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(17): Show |
G | 1 | a0001c0001t0002g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1932-8869_1932-884 others(28): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481633
|
GCTCTCTC others(21): Show |
G | 1 | a0001c0001t0003g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1932-8873_1932-884 others(32): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481633 | |||||
chr17:39481635
|
T | G | 20 | a0001c0001t0002g0082a0001c0001t0003g0052a0001c0001t0003g0062others(17): Show | 20 | HG01517.hp2 HG01975.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1932-8922T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481635 | ||||||
chr17:39481637
|
T | G | 47 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(44): Show | 47 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1932-8920T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481637 | ||||||
chr17:39481639
|
T | G | 6 | a0001c0001t0003g0047a0001c0001t0007g0051a0001c0002t0019g0009others(3): Show | 6 | HG01346.hp2 HG01993.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932-8918T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481639 | ||||||
chr17:39481641
|
T | G | 1 | a0001c0001t0003g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1932-8916T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481641 | ||||||
chr17:39481643
|
T | G | 2 | a0001c0001t0003g0070a0001c0001t0029g0025 | 2 | HG01109.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1932-8914T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481643 | ||||||
chr17:39481645
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1932-8912T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481645 | ||||||
chr17:39481647
|
T | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0080a0001c0001t0003g0053 | 3 | HG00738.hp1 HG00741.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1932-8910T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481647 | ||||||
chr17:39481649
|
T | G | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1932-8908T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481649 | ||||||
chr17:39481651
|
T | G | 3 | a0001c0001t0002g0042a0001c0001t0002g0081a0001c0001t0002g0083 | 3 | HG01123.hp2 HG01515.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1932-8906T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481651 | ||||||
chr17:39481659
|
T | G | 1 | a0001c0001t0002g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1932-8898T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481659 | ||||||
chr17:39481660
|
CTCTCTCT others(45): Show |
C | 9 | a0001c0002t0021g0005a0001c0002t0021g0021a0001c0002t0023g0256others(6): Show | 9 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1932-8891_1932-884 others(56): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481660 | |||||
chr17:39481661
|
T | C | 1 | a0001c0001t0007g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1932-8896T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481661 | ||||||
chr17:39481664
|
CTCTCTCT others(41): Show |
C | 1 | a0001c0001t0011g0105 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1932-8887_1932-884 others(52): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481664 | |||||
chr17:39481666
|
CTCTCTCT others(39): Show |
C | 1 | a0001c0001t0015g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1932-8885_1932-884 others(50): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481666 | |||||
chr17:39481668
|
CTCTCTCT others(37): Show |
C | 4 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0015g0099others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-8883_1932-884 others(48): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481668 | |||||
chr17:39481669
|
TCTCTCTC others(40): Show |
T | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1932-8887_1932-884 others(51): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481669 | ||||||
chr17:39481670
|
CTCTCTCT others(35): Show |
C | 3 | a0001c0001t0012g0093a0001c0001t0012g0095a0001c0002t0059g0012 | 3 | HG01361.hp2 HG04204.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1932-8881_1932-884 others(46): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481670 | |||||
chr17:39481672
|
CTCTCTCT others(33): Show |
C | 1 | a0001c0001t0018g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1932-8879_1932-884 others(44): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481672 | |||||
chr17:39481676
|
CTCTCTCT others(29): Show |
C | 3 | a0001c0001t0013g0109a0001c0001t0040g0114a0001c0001t0052g0111 | 3 | HG02129.hp2 HG02922.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1932-8875_1932-884 others(40): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481676 | |||||
chr17:39481678
|
CTCTCTCT others(27): Show |
C | 8 | a0001c0001t0009g0088a0001c0001t0010g0091a0001c0001t0013g0110others(5): Show | 8 | HG02145.hp2 HG02809.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1932-8873_1932-884 others(38): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481678 | |||||
chr17:39481680
|
CTCTCTCT others(25): Show |
C | 5 | a0001c0001t0013g0112a0001c0001t0037g0090a0001c0001t0038g0089others(2): Show | 5 | HG02280.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932-8871_1932-884 others(36): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481680 | |||||
chr17:39481682
|
CTCTCTCT others(23): Show |
C | 2 | a0001c0001t0009g0087a0001c0002t0019g0009 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1932-8869_1932-884 others(34): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481682 | |||||
chr17:39481682
|
CTCTCTCT others(28): Show |
C | 2 | a0001c0001t0012g0115a0001c0001t0018g0086 | 2 | HG02132.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1932-8873_1932-883 others(39): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481682 | |||||
chr17:39481684
|
CTCTCTCT others(21): Show |
C | 1 | a0006c0008t0035g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1932-8867_1932-884 others(32): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481684 | |||||
chr17:39481686
|
CTCTCTCT others(19): Show |
C | 1 | a0001c0002t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1932-8865_1932-884 others(30): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481686 | |||||
chr17:39481686
|
CTCTCTCT others(24): Show |
C | 1 | a0001c0007t0009g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1932-8869_1932-883 others(35): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481686 | |||||
chr17:39481688
|
CTCTCTCT others(16): Show |
C | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1932-8867_1932-884 others(27): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481688 | |||||
chr17:39481690
|
CTCTCTCT others(14): Show |
C | 1 | a0001c0001t0007g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1932-8865_1932-884 others(25): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481690 | |||||
chr17:39481692
|
CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0034g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1932-8859_1932-884 others(24): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481692 | |||||
chr17:39481694
|
CTCTCTCT others(10): Show |
C | 3 | a0001c0001t0002g0082a0001c0001t0003g0068a0001c0001t0005g0037 | 3 | HG01517.hp2 NA18993.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1932-8861_1932-884 others(21): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481694 | |||||
chr17:39481698
|
CTCTCTCT others(6): Show |
C | 2 | a0001c0001t0003g0052a0001c0001t0005g0033 | 2 | HG02015.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1932-8857_1932-884 others(17): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481698 | |||||
chr17:39481698
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0009g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1932-8853_1932-884 others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481698 | |||||
chr17:39481700
|
CTCTCTCT others(4): Show |
C | 1 | a0001c0001t0004g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1932-8855_1932-884 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481700 | |||||
chr17:39481710
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1932-8847C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481710 | ||||||
chr17:39481712
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1932-8845T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481712 | ||||||
chr17:39481728
|
CTT | C | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1932-8818_1932-881 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481728 | |||||
chr17:39481728
|
CTTT | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1932-8819_1932-881 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39481728 | |||||
chr17:39481761
|
C | G | 11 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932-8796C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481761 | ||||||
chr17:39481998
|
G | A | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1932-8559G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39481998 | ||||||
chr17:39482015
|
C | CATTTTTT others(7): Show |
1 | a0001c0001t0001g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1932-8542_1932-854 others(18): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482015
|
C | CATTTTTT others(8): Show |
25 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0124others(22): Show | 26 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1932-8542_1932-854 others(19): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482015
|
C | CATTTTTT others(9): Show |
63 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0120others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.1932-8542_1932-854 others(20): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482015
|
C | CATTTTTT others(10): Show |
41 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0136others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1932-8542_1932-854 others(21): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482015
|
C | CATTTTTT others(11): Show |
6 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0203others(3): Show | 6 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932-8542_1932-854 others(22): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482015
|
C | CATTTTTT others(12): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0225 | 2 | HG02257.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1932-8542_1932-854 others(23): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482015 | ||||||
chr17:39482043
|
G | A | 11 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932-8514G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482043 | ||||||
chr17:39482175
|
G | A | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-8382G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482175 | ||||||
chr17:39482191
|
T | TAATAGAG others(6): Show |
1 | a0001c0001t0002g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1932-8365_1932-835 others(17): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482191 | |||||
chr17:39482506
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1932-8051G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482506 | ||||||
chr17:39482532
|
C | G | 1 | a0001c0001t0006g0232 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1932-8025C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482532 | ||||||
chr17:39482599
|
A | AT | 11 | a0001c0001t0002g0034a0001c0001t0002g0058a0001c0001t0003g0063others(8): Show | 11 | HG00621.hp2 HG00673.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932-7937dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482599 | |||||
chr17:39482599
|
A | ATTTTTTT others(3): Show |
23 | a0001c0001t0001g0027a0001c0001t0001g0120a0001c0001t0001g0122others(20): Show | 23 | HG00741.hp2 HG01071.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1932-7946_1932-793 others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482599 | |||||
chr17:39482599
|
A | ATTTTTTT others(4): Show |
78 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0001t0001g0125others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.1932-7947_1932-793 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482599 | |||||
chr17:39482599
|
A | ATTTTTTT others(5): Show |
31 | a0001c0001t0001g0001a0001c0001t0001g0133a0001c0001t0001g0135others(28): Show | 32 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1932-7948_1932-793 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482599 | |||||
chr17:39482599
|
A | ATTTTTTT others(6): Show |
5 | a0001c0001t0001g0184a0001c0001t0001g0206a0001c0001t0001g0230others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932-7949_1932-793 others(17): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482599 | |||||
chr17:39482624
|
G | T | 1 | a0001c0001t0003g0070 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1932-7933G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482624 | ||||||
chr17:39482909
|
AT | A | 26 | a0001c0001t0002g0066a0001c0001t0009g0087a0001c0001t0009g0088others(23): Show | 26 | HG01071.hp2 HG01361.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1932-7627delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482909 | |||||
chr17:39482909
|
ATTTTTT | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1932-7632_1932-762 others(10): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39482909 | |||||
chr17:39482984
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0181 | 2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1932-7573C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39482984 | ||||||
chr17:39483074
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1932-7483G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483074 | ||||||
chr17:39483251
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1932-7306A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483251 | ||||||
chr17:39483315
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1932-7242A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483315 | ||||||
chr17:39483367
|
C | T | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-7190C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483367 | ||||||
chr17:39483610
|
GATT | G | 8 | a0001c0002t0021g0005a0001c0002t0023g0256a0001c0002t0023g0257others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1932-6944_1932-694 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39483610 | |||||
chr17:39483631
|
C | T | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1932-6926C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483631 | ||||||
chr17:39483648
|
A | G | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1932-6909A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483648 | ||||||
chr17:39483689
|
A | AATTT | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0201others(7): Show | 10 | HG00423.hp2 HG01109.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1932-6827_1932-682 others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39483689 | |||||
chr17:39483689
|
AATTT | A | 15 | a0001c0001t0002g0076a0001c0001t0003g0078a0001c0001t0005g0003others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1932-6827_1932-682 others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39483689 | |||||
chr17:39483689
|
AATTTATT others(1): Show |
A | 42 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0006g0232others(39): Show | 42 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1932-6831_1932-682 others(12): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39483689 | |||||
chr17:39483689
|
AATTTATT others(5): Show |
A | 4 | a0001c0001t0002g0039a0001c0001t0008g0077a0003c0005t0054g0252others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-6835_1932-682 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39483689 | |||||
chr17:39483753
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1932-6804C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483753 | ||||||
chr17:39483760
|
T | G | 1 | a0001c0007t0009g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1932-6797T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483760 | ||||||
chr17:39483809
|
C | T | 1 | a0005c0010t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1932-6748C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483809 | ||||||
chr17:39483811
|
C | A | 1 | a0003c0005t0054g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1932-6746C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483811 | ||||||
chr17:39483896
|
T | G | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1932-6661T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39483896 | ||||||
chr17:39484574
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1932-5983A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39484574 | ||||||
chr17:39484597
|
G | A | 1 | a0001c0001t0007g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1932-5960G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39484597 | ||||||
chr17:39484998
|
G | A | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1932-5559G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39484998 | ||||||
chr17:39485063
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1932-5494G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485063 | ||||||
chr17:39485100
|
G | A | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101 | 3 | HG02145.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1932-5457G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485100 | ||||||
chr17:39485149
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1932-5408G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485149 | ||||||
chr17:39485169
|
C | CA | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0234others(6): Show | 9 | HG00597.hp1 HG00741.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1932-5369dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485169 | |||||
chr17:39485169
|
C | CAA | 11 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932-5370_1932-536 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485169 | |||||
chr17:39485213
|
T | C | 2 | a0001c0001t0014g0141a0001c0001t0022g0182 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1932-5344T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485213 | ||||||
chr17:39485407
|
C | A | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1932-5150C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485407 | ||||||
chr17:39485408
|
C | CT | 8 | a0001c0001t0002g0058a0001c0001t0002g0080a0001c0001t0003g0031others(5): Show | 8 | HG00597.hp1 HG00621.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1932-5127dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485408 | |||||
chr17:39485408
|
CT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1932-5127delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485408 | |||||
chr17:39485408
|
CTT | C | 12 | a0001c0001t0001g0215a0001c0002t0019g0009a0001c0002t0020g0008others(9): Show | 12 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1932-5128_1932-512 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485408 | |||||
chr17:39485408
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0056g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1932-5138_1932-512 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39485408 | |||||
chr17:39485409
|
T | C | 12 | a0001c0001t0004g0016a0001c0001t0010g0091a0001c0001t0012g0095others(9): Show | 12 | HG02129.hp2 HG02132.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1932-5148T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485409 | ||||||
chr17:39485410
|
T | C | 18 | a0001c0001t0001g0135a0001c0001t0001g0192a0001c0001t0009g0087others(15): Show | 18 | HG02055.hp1 HG02280.hp2 HG02809.hp2 others(15): Show |
intron_variant | MODIFIER | c.1932-5147T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485410 | ||||||
chr17:39485411
|
T | C | 1 | a0001c0001t0017g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1932-5146T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485411 | ||||||
chr17:39485417
|
T | C | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101 | 3 | HG02145.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1932-5140T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485417 | ||||||
chr17:39485565
|
A | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4992A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485565 | ||||||
chr17:39485566
|
C | G | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4991C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485566 | ||||||
chr17:39485567
|
C | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4990C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485567 | ||||||
chr17:39485568
|
A | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4989A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485568 | ||||||
chr17:39485569
|
C | A | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4988C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485569 | ||||||
chr17:39485569
|
C | T | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1932-4988C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485569 | ||||||
chr17:39485571
|
C | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1932-4986C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485571 | ||||||
chr17:39485605
|
G | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1932-4952G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485605 | ||||||
chr17:39485614
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1932-4943A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39485614 | ||||||
chr17:39486014
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0223 | 2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1932-4543G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486014 | ||||||
chr17:39486110
|
G | T | 1 | a0001c0001t0012g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1932-4447G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486110 | ||||||
chr17:39486144
|
G | A | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1932-4413G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486144 | ||||||
chr17:39486253
|
C | CT | 18 | a0001c0001t0002g0034a0001c0001t0003g0070a0001c0001t0008g0041others(15): Show | 18 | HG00673.hp2 HG01109.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1932-4282dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39486253 | |||||
chr17:39486253
|
CT | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1932-4282delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39486253 | |||||
chr17:39486340
|
C | T | 1 | a0001c0001t0006g0191 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1932-4217C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486340 | ||||||
chr17:39486493
|
C | T | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-4064C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486493 | ||||||
chr17:39486865
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1932-3692G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39486865 | ||||||
chr17:39487003
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1932-3554G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487003 | ||||||
chr17:39487123
|
C | G | 7 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0211others(4): Show | 7 | HG01069.hp1 HG01993.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1932-3434C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487123 | ||||||
chr17:39487400
|
T | C | 4 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0011g0105others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-3157T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487400 | ||||||
chr17:39487413
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1932-3144C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487413 | ||||||
chr17:39487524
|
A | C | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1932-3033A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487524 | ||||||
chr17:39487607
|
A | AT | 41 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0144others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.1932-2923dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39487607 | |||||
chr17:39487607
|
A | ATT | 6 | a0001c0001t0001g0178a0001c0001t0001g0248a0001c0001t0003g0068others(3): Show | 6 | HG00738.hp2 HG01981.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1932-2924_1932-292 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39487607 | |||||
chr17:39487607
|
AT | A | 38 | a0001c0001t0001g0136a0001c0001t0001g0194a0001c0001t0001g0213others(35): Show | 38 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1932-2923delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39487607 | |||||
chr17:39487607
|
ATT | A | 17 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(14): Show | 17 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1932-2924_1932-292 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39487607 | |||||
chr17:39487607
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0235 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1932-2934_1932-292 others(16): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39487607 | |||||
chr17:39487610
|
T | C | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1932-2947T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487610 | ||||||
chr17:39487694
|
G | A | 1 | a0001c0001t0027g0029 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1932-2863G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487694 | ||||||
chr17:39487859
|
C | T | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1932-2698C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487859 | ||||||
chr17:39487878
|
G | A | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1932-2679G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39487878 | ||||||
chr17:39488134
|
T | C | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1932-2423T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488134 | ||||||
chr17:39488270
|
C | G | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1932-2287C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488270 | ||||||
chr17:39488360
|
A | G | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1932-2197A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488360 | ||||||
chr17:39488460
|
G | A | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1932-2097G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488460 | ||||||
chr17:39488601
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1932-1956C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488601 | ||||||
chr17:39488876
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1932-1681C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39488876 | ||||||
chr17:39489079
|
A | AT | 10 | a0001c0001t0002g0039a0001c0001t0002g0076a0001c0001t0003g0052others(7): Show | 10 | HG02258.hp2 HG02300.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1932-1460dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39489079 | |||||
chr17:39489165
|
C | G | 18 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(15): Show | 18 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1932-1392C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489165 | ||||||
chr17:39489173
|
G | T | 1 | a0001c0001t0052g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1932-1384G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489173 | ||||||
chr17:39489184
|
A | C | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1932-1373A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489184 | ||||||
chr17:39489193
|
G | A | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-1364G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489193 | ||||||
chr17:39489307
|
C | T | 3 | a0001c0001t0009g0108a0001c0001t0034g0097a0001c0001t0036g0092 | 3 | HG02809.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1932-1250C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489307 | ||||||
chr17:39489727
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0006g0253 | 3 | HG01255.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1932-830C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489727 | ||||||
chr17:39489794
|
A | AT | 145 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0120others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1932-745dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39489794 | |||||
chr17:39489926
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1932-631C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489926 | ||||||
chr17:39489986
|
G | A | 7 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(4): Show | 7 | HG00621.hp1 HG01106.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.1932-571G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39489986 | ||||||
chr17:39490104
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0192a0001c0001t0001g0196 | 3 | HG00621.hp1 NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1932-453C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490104 | ||||||
chr17:39490132
|
C | T | 18 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(15): Show | 18 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1932-425C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490132 | ||||||
chr17:39490304
|
T | G | 1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1932-253T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490304 | ||||||
chr17:39490323
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0048g0189 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1932-234C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490323 | ||||||
chr17:39490336
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1932-221T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490336 | ||||||
chr17:39490366
|
C | CA | 16 | a0001c0001t0002g0066a0001c0002t0019g0009a0001c0002t0020g0008others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1932-181dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 39490366 | |||||
chr17:39490450
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1932-107A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 2/13 | chr17 | 39490450 | ||||||
chr17:39490789
|
T | A | 4 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0011g0105others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108+56T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39490789 | ||||||
chr17:39490993
|
G | A | 1 | a0001c0002t0023g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108+260G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39490993 | ||||||
chr17:39491006
|
A | G | 2 | a0001c0002t0021g0005a0001c0002t0043g0006 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2108+273A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491006 | ||||||
chr17:39491014
|
T | TA | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2108+282dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39491014 | |||||
chr17:39491027
|
A | AAGAATAA others(468): Show |
1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2108+310_2108+311i others(477): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39491027 | |||||
chr17:39491053
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2108+320A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491053 | ||||||
chr17:39491093
|
A | C | 3 | a0001c0001t0027g0029a0001c0001t0027g0048a0001c0001t0056g0067 | 3 | HG00140.hp1 HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2108+360A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491093 | ||||||
chr17:39491197
|
A | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2108+464A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491197 | ||||||
chr17:39491318
|
A | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2108+585A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491318 | ||||||
chr17:39491361
|
C | T | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2108+628C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491361 | ||||||
chr17:39491463
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2108+730T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491463 | ||||||
chr17:39491482
|
C | T | 1 | a0001c0001t0013g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2108+749C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491482 | ||||||
chr17:39491483
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2108+750G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491483 | ||||||
chr17:39491502
|
C | T | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108+769C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491502 | ||||||
chr17:39491513
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2108+780G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491513 | ||||||
chr17:39491701
|
A | AT | 20 | a0001c0001t0002g0255a0001c0001t0003g0063a0001c0001t0004g0013others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2108+987dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39491701 | |||||
chr17:39491701
|
AT | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0142a0001c0001t0001g0169others(8): Show | 11 | HG01256.hp1 HG02451.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.2108+987delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39491701 | |||||
chr17:39491832
|
A | G | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109-919A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491832 | ||||||
chr17:39491887
|
G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.2109-864G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491887 | ||||||
chr17:39491897
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2109-854G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491897 | ||||||
chr17:39491939
|
C | T | 1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2109-812C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39491939 | ||||||
chr17:39492012
|
C | CT | 3 | a0001c0001t0001g0184a0001c0001t0001g0233a0001c0001t0026g0148 | 3 | HG01433.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2109-738dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39492012 | |||||
chr17:39492013
|
T | TA | 6 | a0001c0001t0002g0034a0001c0001t0002g0042a0001c0001t0004g0079others(3): Show | 6 | HG00673.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2109-720dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39492013 | |||||
chr17:39492014
|
A | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2109-737A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39492014 | ||||||
chr17:39492015
|
A | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0205a0003c0005t0054g0252others(1): Show | 4 | HG01109.hp1 HG01943.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109-736A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39492015 | ||||||
chr17:39492099
|
C | CT | 13 | a0001c0001t0001g0153a0001c0001t0003g0065a0001c0001t0004g0013others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2109-637dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 39492099 | |||||
chr17:39492263
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2109-488A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39492263 | ||||||
chr17:39492266
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2109-485T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39492266 | ||||||
chr17:39492718
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2109-33T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 3/13 | chr17 | 39492718 | ||||||
chr17:39492985
|
T | TTTTGTTT others(17): Show |
1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2248+99_2248+122du others(25): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39492985 | |||||
chr17:39493009
|
G | GT | 9 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0004g0013others(6): Show | 9 | HG02109.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2248+125dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39493009 | |||||
chr17:39493139
|
G | A | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2248+249G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493139 | ||||||
chr17:39493166
|
G | GT | 16 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0001t0001g0195others(13): Show | 16 | HG00621.hp1 HG01515.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2248+292dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39493166 | |||||
chr17:39493166
|
G | GTT | 111 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.2248+291_2248+292d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39493166 | |||||
chr17:39493166
|
G | GTTT | 6 | a0001c0001t0001g0178a0001c0001t0001g0201a0001c0001t0001g0224others(3): Show | 6 | HG00423.hp2 HG02055.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2248+290_2248+292d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39493166 | |||||
chr17:39493166
|
G | T | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2248+276G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493166 | ||||||
chr17:39493174
|
T | TTG | 20 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0142others(17): Show | 20 | HG01106.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2248+285_2248+286i others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 39493174 | |||||
chr17:39493254
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2248+364C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493254 | ||||||
chr17:39493434
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2248+544G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493434 | ||||||
chr17:39493639
|
A | C | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2248+749A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493639 | ||||||
chr17:39493701
|
C | T | 1 | a0001c0001t0046g0180 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2248+811C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493701 | ||||||
chr17:39493824
|
G | A | 1 | a0001c0001t0053g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2249-700G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493824 | ||||||
chr17:39493951
|
G | A | 1 | a0001c0001t0039g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2249-573G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493951 | ||||||
chr17:39493963
|
T | C | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2249-561T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39493963 | ||||||
chr17:39494051
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2249-473A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494051 | ||||||
chr17:39494062
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2249-462T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494062 | ||||||
chr17:39494079
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2249-445A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494079 | ||||||
chr17:39494080
|
A | G | 1 | a0003c0005t0055g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2249-444A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494080 | ||||||
chr17:39494167
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2249-357G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494167 | ||||||
chr17:39494230
|
C | T | 9 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0004g0013others(6): Show | 9 | HG02109.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2249-294C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494230 | ||||||
chr17:39494316
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2249-208G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494316 | ||||||
chr17:39494493
|
T | C | 1 | a0001c0001t0005g0003 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2249-31T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 4/13 | chr17 | 39494493 | ||||||
chr17:39494773
|
C | CT | 18 | a0001c0001t0001g0224a0001c0001t0003g0052a0001c0001t0009g0087others(15): Show | 18 | HG02055.hp1 HG02071.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2419+93dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39494773 | |||||
chr17:39494811
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2419+117C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39494811 | ||||||
chr17:39494870
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2419+176C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39494870 | ||||||
chr17:39494871
|
G | A | 1 | a0001c0001t0024g0254 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2419+177G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39494871 | ||||||
chr17:39494974
|
T | C | 1 | a0001c0001t0003g0047 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2419+280T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39494974 | ||||||
chr17:39494988
|
G | A | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2419+294G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39494988 | ||||||
chr17:39495018
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2419+324G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495018 | ||||||
chr17:39495110
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2419+416G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495110 | ||||||
chr17:39495121
|
C | T | 1 | a0001c0002t0021g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2419+427C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495121 | ||||||
chr17:39495278
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2419+584A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495278 | ||||||
chr17:39495341
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2419+647G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495341 | ||||||
chr17:39495384
|
GT | G | 24 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0034others(21): Show | 24 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.2419+722delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39495384 | |||||
chr17:39495384
|
GTT | G | 56 | a0001c0001t0001g0128a0001c0001t0001g0160a0001c0001t0001g0188others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.2419+721_2419+722d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39495384 | |||||
chr17:39495384
|
GTTT | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2419+720_2419+722d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39495384 | |||||
chr17:39495384
|
GTTTT | G | 11 | a0001c0001t0010g0091a0001c0001t0011g0104a0001c0001t0012g0095others(8): Show | 11 | HG01070.hp1 HG02129.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2419+719_2419+722d others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39495384 | |||||
chr17:39495389
|
T | G | 4 | a0001c0001t0003g0002a0002c0003t0016g0117a0002c0003t0016g0118others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.2419+695T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495389 | ||||||
chr17:39495390
|
T | G | 16 | a0001c0001t0001g0128a0001c0001t0001g0160a0001c0001t0001g0188others(13): Show | 16 | HG01192.hp2 HG01952.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2419+696T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495390 | ||||||
chr17:39495391
|
T | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2419+697T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495391 | ||||||
chr17:39495392
|
T | G | 11 | a0001c0001t0010g0091a0001c0001t0011g0104a0001c0001t0012g0095others(8): Show | 11 | HG01070.hp1 HG02129.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2419+698T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495392 | ||||||
chr17:39495394
|
T | G | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2419+700T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495394 | ||||||
chr17:39495395
|
T | G | 10 | a0001c0002t0021g0005a0001c0002t0021g0021a0001c0002t0023g0256others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2419+701T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495395 | ||||||
chr17:39495397
|
T | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0160a0001c0001t0001g0188 | 3 | HG01952.hp2 HG02523.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2419+703T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495397 | ||||||
chr17:39495398
|
T | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2419+704T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495398 | ||||||
chr17:39495443
|
A | G | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2419+749A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495443 | ||||||
chr17:39495448
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2419+754G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495448 | ||||||
chr17:39495468
|
A | G | 1 | a0008c0009t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2419+774A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495468 | ||||||
chr17:39495652
|
G | A | 2 | a0001c0002t0020g0011a0001c0002t0041g0010 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2419+958G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495652 | ||||||
chr17:39495667
|
C | T | 1 | a0001c0001t0026g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2419+973C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495667 | ||||||
chr17:39495687
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2419+993C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495687 | ||||||
chr17:39495727
|
G | A | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101 | 3 | HG02145.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2419+1033G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495727 | ||||||
chr17:39495736
|
G | A | 1 | a0001c0002t0023g0257 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2419+1042G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495736 | ||||||
chr17:39495750
|
G | A | 1 | a0008c0009t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2419+1056G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495750 | ||||||
chr17:39495789
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0181 | 2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.2419+1095C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495789 | ||||||
chr17:39495794
|
CA | C | 5 | a0001c0001t0002g0082a0001c0001t0005g0024a0001c0001t0006g0139others(2): Show | 5 | HG01496.hp1 HG01517.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2419+1116delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39495794 | |||||
chr17:39495925
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2419+1231T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495925 | ||||||
chr17:39495957
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2419+1263G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39495957 | ||||||
chr17:39496154
|
A | G | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2419+1460A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496154 | ||||||
chr17:39496176
|
G | A | 68 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0001g0133others(65): Show | 68 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2419+1482G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496176 | ||||||
chr17:39496204
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2419+1510C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496204 | ||||||
chr17:39496453
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2419+1759A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496453 | ||||||
chr17:39496590
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2419+1896A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496590 | ||||||
chr17:39496658
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2419+1964G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496658 | ||||||
chr17:39496862
|
A | G | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2419+2168A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496862 | ||||||
chr17:39496912
|
C | CT | 22 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0002g0026others(19): Show | 22 | HG00741.hp1 HG01192.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.2419+2248dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39496912 | |||||
chr17:39496912
|
CT | C | 22 | a0001c0001t0002g0036a0001c0001t0002g0066a0001c0001t0002g0082others(19): Show | 22 | HG00140.hp1 HG01070.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2419+2248delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39496912 | |||||
chr17:39496912
|
CTTTTTT | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0210a0001c0001t0001g0226others(2): Show | 5 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2419+2243_2419+224 others(10): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39496912 | |||||
chr17:39496912
|
CTTTTTTT | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2419+2242_2419+224 others(11): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39496912 | |||||
chr17:39496912
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0120a0001c0001t0001g0142a0001c0001t0001g0157others(5): Show | 8 | HG01069.hp1 HG01496.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.2419+2241_2419+224 others(12): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39496912 | |||||
chr17:39496942
|
T | A | 1 | a0001c0001t0006g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2419+2248T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39496942 | ||||||
chr17:39497147
|
G | A | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2419+2453G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497147 | ||||||
chr17:39497361
|
T | C | 1 | a0001c0001t0015g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2419+2667T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497361 | ||||||
chr17:39497426
|
C | T | 2 | a0001c0002t0020g0011a0001c0002t0041g0010 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2419+2732C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497426 | ||||||
chr17:39497482
|
G | T | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2419+2788G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497482 | ||||||
chr17:39497483
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2419+2789C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497483 | ||||||
chr17:39497908
|
G | A | 1 | a0001c0001t0052g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2419+3214G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39497908 | ||||||
chr17:39498006
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2420-3244T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498006 | ||||||
chr17:39498011
|
CT | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2420-3229delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498011 | |||||
chr17:39498012
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2420-3238T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498012 | ||||||
chr17:39498232
|
G | GT | 6 | a0001c0001t0002g0066a0001c0001t0002g0081a0001c0001t0003g0068others(3): Show | 6 | HG01123.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2420-3008dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498232 | |||||
chr17:39498470
|
G | A | 1 | a0001c0001t0007g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2420-2780G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498470 | ||||||
chr17:39498470
|
G | GCCTCGGC others(4): Show |
1 | a0001c0001t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2420-2778_2420-276 others(15): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498470 | |||||
chr17:39498503
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0242 | 2 | NA18959.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2420-2747G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498503 | ||||||
chr17:39498518
|
C | T | 3 | a0001c0001t0007g0072a0001c0001t0007g0074a0001c0001t0030g0073 | 3 | HG02717.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2420-2732C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498518 | ||||||
chr17:39498529
|
C | T | 1 | a0007c0006t0019g0007 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2420-2721C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498529 | ||||||
chr17:39498769
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2420-2481C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498769 | ||||||
chr17:39498869
|
TTTTCTCT others(279): Show |
T | 1 | a0001c0001t0014g0159 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2420-2375_2420-209 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498869 | |||||
chr17:39498871
|
TTC | T | 3 | a0001c0001t0002g0028a0001c0001t0027g0048a0001c0001t0056g0067 | 3 | HG00140.hp1 HG01192.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2420-2375_2420-237 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498871 | |||||
chr17:39498873
|
CTCTTTCT others(164): Show |
C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2375_2420-220 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498873 | |||||
chr17:39498873
|
CTCTTTCT others(196): Show |
C | 1 | a0001c0001t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2420-2375_2420-217 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498873 | |||||
chr17:39498873
|
CTCTTTCT others(197): Show |
C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2246_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498873 | |||||
chr17:39498874
|
TC | T | 13 | a0001c0001t0005g0033a0001c0001t0007g0084a0001c0002t0019g0009others(10): Show | 13 | HG02015.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2420-2375delC | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498874 | ||||||
chr17:39498875
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2420-2375C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498875 | ||||||
chr17:39498877
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0066a0001c0001t0010g0106 | 3 | HG02976.hp1 NA19054.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2373T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498877 | ||||||
chr17:39498879
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2420-2371C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498879 | ||||||
chr17:39498879
|
CT | C | 3 | a0001c0002t0023g0256a0001c0002t0025g0258a0001c0002t0025g0259 | 3 | HG02622.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2420-2368delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498879 | |||||
chr17:39498880
|
T | C | 3 | a0001c0002t0021g0021a0001c0002t0023g0257a0001c0002t0042g0020 | 3 | HG02559.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2420-2370T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498880 | ||||||
chr17:39498883
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2420-2367C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498883 | ||||||
chr17:39498884
|
T | C | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2420-2366T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498884 | ||||||
chr17:39498886
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0255 | 2 | HG01516.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2364T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498886 | ||||||
chr17:39498888
|
T | C | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2420-2362T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498888 | ||||||
chr17:39498888
|
TTTCTTTC others(112): Show |
T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2359_2420-224 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498888 | |||||
chr17:39498890
|
T | C | 7 | a0001c0001t0002g0042a0001c0001t0002g0059a0001c0001t0003g0049others(4): Show | 7 | HG00423.hp1 HG00597.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420-2360T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498890 | ||||||
chr17:39498892
|
T | C | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2420-2358T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498892 | ||||||
chr17:39498892
|
T | TTCCTTCC others(312): Show |
1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2357_2420-235 others(323): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498892 | |||||
chr17:39498894
|
T | C | 26 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2420-2356T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498894 | ||||||
chr17:39498896
|
T | C | 15 | a0001c0001t0002g0066a0001c0002t0019g0009a0001c0002t0020g0008others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2420-2354T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498896 | ||||||
chr17:39498898
|
T | C | 8 | a0001c0001t0002g0042a0001c0001t0002g0059a0001c0001t0003g0049others(5): Show | 8 | HG00423.hp1 HG00597.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2420-2352T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498898 | ||||||
chr17:39498900
|
T | C | 15 | a0001c0001t0002g0066a0001c0002t0019g0009a0001c0002t0020g0008others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2420-2350T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498900 | ||||||
chr17:39498902
|
T | C | 12 | a0001c0001t0002g0042a0001c0001t0002g0059a0001c0001t0003g0031others(9): Show | 12 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2420-2348T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498902 | ||||||
chr17:39498904
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2346T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498904 | ||||||
chr17:39498906
|
T | C | 21 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(18): Show | 21 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2420-2344T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498906 | ||||||
chr17:39498908
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2342T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498908 | ||||||
chr17:39498908
|
TTTCTTTC others(293): Show |
T | 1 | a0001c0001t0018g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2420-2339_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498908 | |||||
chr17:39498910
|
T | C | 23 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2420-2340T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498910 | ||||||
chr17:39498910
|
TCTTTCTT others(290): Show |
T | 1 | a0001c0001t0013g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2420-2335_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498910 | |||||
chr17:39498912
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2338T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498912 | ||||||
chr17:39498912
|
TTTCTTTC others(289): Show |
T | 7 | a0001c0001t0001g0243a0001c0001t0010g0091a0001c0001t0012g0095others(4): Show | 7 | HG02129.hp2 HG02132.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420-2335_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498912 | |||||
chr17:39498913
|
TTCTTTCT others(288): Show |
T | 1 | a0001c0001t0052g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2420-2335_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498913 | |||||
chr17:39498914
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2336T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498914 | ||||||
chr17:39498915
|
CTTTCTTT others(289): Show |
C | 2 | a0002c0003t0016g0118a0002c0003t0016g0119 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2420-2331_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498915 | |||||
chr17:39498916
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2334T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498916 | ||||||
chr17:39498916
|
TTTCTTTC others(285): Show |
T | 1 | a0001c0001t0011g0105 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2420-2331_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498916 | |||||
chr17:39498917
|
TTCTTTCT others(284): Show |
T | 2 | a0001c0001t0001g0220a0001c0001t0012g0093 | 2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2420-2331_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498917 | |||||
chr17:39498918
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2332T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498918 | ||||||
chr17:39498919
|
CTTTCTTT others(285): Show |
C | 1 | a0002c0003t0016g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2420-2327_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498919 | |||||
chr17:39498920
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2330T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498920 | ||||||
chr17:39498920
|
TTTCTTTC others(281): Show |
T | 13 | a0001c0001t0001g0146a0001c0001t0001g0183a0001c0001t0009g0087others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2420-2327_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498920 | |||||
chr17:39498921
|
TTCTTTCT others(280): Show |
T | 6 | a0001c0001t0001g0219a0001c0001t0009g0108a0001c0001t0015g0100others(3): Show | 6 | HG01109.hp1 HG01192.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2420-2327_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498921 | |||||
chr17:39498922
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2328T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498922 | ||||||
chr17:39498922
|
TCTTTCTT others(279): Show |
T | 2 | a0001c0001t0015g0101a0001c0007t0009g0098 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2420-2327_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498922 | ||||||
chr17:39498923
|
C | G | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2327C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498923 | ||||||
chr17:39498923
|
CTTTCTTT others(280): Show |
C | 1 | a0001c0001t0034g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2420-2323_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498923 | |||||
chr17:39498924
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2326T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498924 | ||||||
chr17:39498924
|
TTTCTTTC others(277): Show |
T | 23 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0144others(20): Show | 23 | HG00099.hp1 HG00621.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.2420-2323_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498924 | |||||
chr17:39498925
|
TTCTTTCT others(276): Show |
T | 8 | a0001c0001t0001g0135a0001c0001t0001g0154a0001c0001t0001g0173others(5): Show | 8 | HG00597.hp2 HG01074.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2420-2323_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498925 | |||||
chr17:39498926
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2324T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498926 | ||||||
chr17:39498927
|
CTTTCTTT others(277): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2420-2319_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498927 | |||||
chr17:39498928
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2322T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498928 | ||||||
chr17:39498928
|
TTTCTTTC others(273): Show |
T | 15 | a0001c0001t0001g0153a0001c0001t0001g0170a0001c0001t0001g0172others(12): Show | 15 | HG00558.hp1 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2420-2319_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498928 | |||||
chr17:39498929
|
T | G | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2420-2321T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498929 | ||||||
chr17:39498929
|
TTCTTTCT others(272): Show |
T | 20 | a0001c0001t0001g0001a0001c0001t0001g0131a0001c0001t0001g0132others(17): Show | 21 | HG00099.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2420-2319_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498929 | |||||
chr17:39498930
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2320T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498930 | ||||||
chr17:39498930
|
TCTTTCTT others(270): Show |
T | 3 | a0001c0001t0001g0136a0001c0001t0006g0190a0001c0001t0047g0165 | 3 | HG03834.hp1 HG03834.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.2420-2315_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498930 | |||||
chr17:39498930
|
TCTTTCTT others(271): Show |
T | 4 | a0001c0001t0001g0137a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2319_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498930 | ||||||
chr17:39498931
|
CTTTCTTT others(271): Show |
C | 1 | a0001c0001t0008g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2420-2315_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498931 | |||||
chr17:39498932
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2318T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498932 | ||||||
chr17:39498932
|
TTTCTTTC others(269): Show |
T | 13 | a0001c0001t0001g0133a0001c0001t0001g0142a0001c0001t0001g0168others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2420-2315_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498932 | |||||
chr17:39498933
|
TTCTTTCT others(268): Show |
T | 15 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0164others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2420-2315_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498933 | |||||
chr17:39498934
|
T | C | 26 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2420-2316T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498934 | ||||||
chr17:39498934
|
TCTTTCTT others(266): Show |
T | 2 | a0001c0001t0001g0201a0001c0001t0001g0205 | 2 | HG00423.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2420-2311_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498934 | |||||
chr17:39498934
|
TCTTTCTT others(267): Show |
T | 2 | a0001c0001t0001g0184a0001c0001t0001g0206 | 2 | HG02886.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2420-2315_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498934 | ||||||
chr17:39498935
|
CTTTCTTT others(267): Show |
C | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2420-2311_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498935 | |||||
chr17:39498936
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2314T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498936 | ||||||
chr17:39498936
|
TTTCTTTC others(265): Show |
T | 5 | a0001c0001t0001g0035a0001c0001t0003g0002a0001c0001t0007g0074others(2): Show | 5 | HG01257.hp2 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2420-2311_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498936 | |||||
chr17:39498937
|
TTCTTTCT others(264): Show |
T | 9 | a0001c0001t0001g0122a0001c0001t0001g0166a0001c0001t0001g0197others(6): Show | 9 | HG00735.hp2 HG01943.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2420-2311_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498937 | |||||
chr17:39498938
|
T | C | 26 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2420-2312T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498938 | ||||||
chr17:39498938
|
TCTTTCTT others(262): Show |
T | 1 | a0001c0001t0001g0027 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2420-2307_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498938 | |||||
chr17:39498938
|
TCTTTCTT others(263): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2420-2311_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498938 | ||||||
chr17:39498939
|
CTTTCTTT others(263): Show |
C | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2420-2307_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498939 | |||||
chr17:39498940
|
T | C | 16 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(13): Show | 16 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2420-2310T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498940 | ||||||
chr17:39498940
|
TTTCTTTC others(224): Show |
T | 1 | a0001c0001t0004g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2420-2307_2420-207 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498940 | |||||
chr17:39498940
|
TTTCTTTC others(261): Show |
T | 5 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0194others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-2307_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498940 | |||||
chr17:39498941
|
TTCTTTCT others(260): Show |
T | 4 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0014g0130others(1): Show | 4 | HG01433.hp1 HG02004.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2420-2307_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498941 | |||||
chr17:39498942
|
T | C | 25 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(22): Show | 25 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2420-2308T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498942 | ||||||
chr17:39498942
|
TCTTTCTT others(259): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2420-2307_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498942 | ||||||
chr17:39498943
|
CTTTCTTT others(191): Show |
C | 1 | a0001c0001t0005g0003 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2420-2305_2420-210 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498943 | |||||
chr17:39498944
|
T | C | 11 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(8): Show | 11 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2420-2306T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498944 | ||||||
chr17:39498944
|
TTTCTTTC others(220): Show |
T | 1 | a0001c0001t0004g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2420-2303_2420-207 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498944 | |||||
chr17:39498944
|
TTTCTTTC others(257): Show |
T | 3 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0044 | 3 | HG01884.hp2 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2420-2303_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498944 | |||||
chr17:39498945
|
T | C | 1 | a0001c0001t0027g0029 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2420-2305T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498945 | ||||||
chr17:39498945
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2305T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498945 | ||||||
chr17:39498945
|
TTCTTTCT others(256): Show |
T | 2 | a0001c0001t0001g0124a0001c0001t0001g0210 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2420-2303_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498945 | |||||
chr17:39498946
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2304T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498946 | ||||||
chr17:39498946
|
TCTTTCTT others(254): Show |
T | 1 | a0001c0001t0051g0187 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2420-2299_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498946 | |||||
chr17:39498946
|
TCTTTCTT others(255): Show |
T | 1 | a0001c0001t0001g0121 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2420-2303_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498946 | ||||||
chr17:39498947
|
CTTTCTTT others(255): Show |
C | 1 | a0001c0001t0010g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2420-2299_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498947 | |||||
chr17:39498948
|
T | C | 9 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(6): Show | 9 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2420-2302T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498948 | ||||||
chr17:39498948
|
TTTCTTTC others(216): Show |
T | 2 | a0001c0001t0004g0014a0001c0001t0004g0017 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2420-2299_2420-207 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498948 | |||||
chr17:39498948
|
TTTCTTTC others(253): Show |
T | 1 | a0001c0001t0005g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2420-2299_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498948 | |||||
chr17:39498949
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2301T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498949 | ||||||
chr17:39498949
|
TTCTTTCT others(252): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2420-2299_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498949 | |||||
chr17:39498950
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2300T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498950 | ||||||
chr17:39498950
|
TCTTTCTT others(250): Show |
T | 1 | a0001c0001t0003g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2420-2295_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498950 | |||||
chr17:39498951
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2299C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498951 | ||||||
chr17:39498951
|
CTTTCTTT others(251): Show |
C | 1 | a0001c0001t0003g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2420-2295_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498951 | |||||
chr17:39498952
|
T | C | 7 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(4): Show | 7 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2420-2298T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498952 | ||||||
chr17:39498952
|
TTTCTTTC others(212): Show |
T | 1 | a0001c0001t0002g0018 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2420-2295_2420-207 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498952 | |||||
chr17:39498952
|
TTTCTTTC others(228): Show |
T | 1 | a0001c0001t0027g0029 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2420-2295_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498952 | |||||
chr17:39498953
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2297T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498953 | ||||||
chr17:39498954
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2296T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498954 | ||||||
chr17:39498956
|
T | C | 6 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(3): Show | 6 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2294T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498956 | ||||||
chr17:39498957
|
T | C | 2 | a0001c0001t0027g0048a0001c0001t0056g0067 | 2 | HG00140.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2420-2293T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498957 | ||||||
chr17:39498957
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2293T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498957 | ||||||
chr17:39498958
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2292T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498958 | ||||||
chr17:39498959
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2291C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498959 | ||||||
chr17:39498960
|
T | C | 6 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(3): Show | 6 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2290T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498960 | ||||||
chr17:39498961
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2289T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498961 | ||||||
chr17:39498962
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2288T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498962 | ||||||
chr17:39498963
|
CTTTCTTT others(241): Show |
C | 1 | a0001c0002t0021g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2420-2283_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498963 | |||||
chr17:39498964
|
T | C | 6 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(3): Show | 6 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2286T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498964 | ||||||
chr17:39498964
|
TTTCTTTC others(216): Show |
T | 2 | a0001c0001t0027g0048a0001c0001t0056g0067 | 2 | HG00140.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2420-2283_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498964 | |||||
chr17:39498965
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2285T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498965 | ||||||
chr17:39498966
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2284T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498966 | ||||||
chr17:39498967
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2283C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498967 | ||||||
chr17:39498968
|
T | C | 6 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(3): Show | 6 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2282T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498968 | ||||||
chr17:39498969
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2281T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498969 | ||||||
chr17:39498969
|
TTCTTTCT others(232): Show |
T | 1 | a0001c0001t0002g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2420-2279_2420-204 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498969 | |||||
chr17:39498970
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2280T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498970 | ||||||
chr17:39498971
|
CTTTCTTT others(233): Show |
C | 1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2420-2275_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498971 | |||||
chr17:39498972
|
T | C | 7 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0028g0022others(4): Show | 7 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2420-2278T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498972 | ||||||
chr17:39498973
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2277T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498973 | ||||||
chr17:39498974
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2276T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498974 | ||||||
chr17:39498975
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2275C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498975 | ||||||
chr17:39498975
|
CTTTCTTT others(229): Show |
C | 4 | a0001c0002t0023g0256a0001c0002t0025g0258a0001c0002t0025g0259others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2271_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498975 | |||||
chr17:39498976
|
T | C | 7 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0028g0022others(4): Show | 7 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2420-2274T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498976 | ||||||
chr17:39498977
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2273T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498977 | ||||||
chr17:39498978
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2272T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498978 | ||||||
chr17:39498979
|
CTTTCTTT others(225): Show |
C | 3 | a0001c0002t0021g0005a0001c0002t0023g0257a0001c0002t0043g0006 | 3 | HG03225.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2420-2267_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498979 | |||||
chr17:39498980
|
T | C | 8 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0005g0037others(5): Show | 8 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2420-2270T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498980 | ||||||
chr17:39498981
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2269T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498981 | ||||||
chr17:39498982
|
T | C | 25 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(22): Show | 25 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2420-2268T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498982 | ||||||
chr17:39498983
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2267C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498983 | ||||||
chr17:39498983
|
CTTTCTTT others(221): Show |
C | 1 | a0001c0002t0049g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2420-2263_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498983 | |||||
chr17:39498983
|
CTTTCTTT others(222): Show |
C | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2420-2263_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498983 | |||||
chr17:39498984
|
T | C | 5 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0002t0019g0009others(2): Show | 5 | HG02451.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2420-2266T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498984 | ||||||
chr17:39498986
|
T | C | 24 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2420-2264T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498986 | ||||||
chr17:39498988
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0005g0037 | 3 | NA19002.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2420-2262T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498988 | ||||||
chr17:39498990
|
T | C | 23 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2420-2260T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498990 | ||||||
chr17:39498991
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2259C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498991 | ||||||
chr17:39498992
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0028g0022 | 3 | NA18940.hp2 NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2258T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498992 | ||||||
chr17:39498994
|
T | C | 21 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(18): Show | 21 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2420-2256T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498994 | ||||||
chr17:39498996
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0005g0037 | 3 | NA19002.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2420-2254T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498996 | ||||||
chr17:39498998
|
T | C | 21 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(18): Show | 21 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2420-2252T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498998 | ||||||
chr17:39498999
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2251C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39498999 | ||||||
chr17:39498999
|
CTTTCTTT others(205): Show |
C | 1 | a0001c0002t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2420-2247_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39498999 | |||||
chr17:39499000
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0003g0070 | 2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2250T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499000 | ||||||
chr17:39499002
|
T | C | 18 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(15): Show | 18 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2420-2248T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499002 | ||||||
chr17:39499003
|
CTTTCTTT others(201): Show |
C | 3 | a0001c0002t0019g0009a0001c0002t0020g0011a0001c0002t0041g0010 | 3 | HG02451.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2420-2243_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499003 | |||||
chr17:39499004
|
T | C | 4 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0005g0037others(1): Show | 4 | NA18940.hp2 NA19002.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2420-2246T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499004 | ||||||
chr17:39499006
|
T | C | 18 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(15): Show | 18 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2420-2244T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499006 | ||||||
chr17:39499007
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2243C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499007 | ||||||
chr17:39499007
|
CTTTCTTT others(212): Show |
C | 1 | a0001c0001t0002g0026 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2420-2242_2420-202 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499007 | ||||||
chr17:39499008
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0003g0070 | 2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2242T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499008 | ||||||
chr17:39499010
|
T | C | 15 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(12): Show | 15 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.2420-2240T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499010 | ||||||
chr17:39499012
|
T | C | 4 | a0001c0001t0002g0066a0001c0001t0003g0070a0001c0001t0005g0037others(1): Show | 4 | NA18940.hp2 NA19002.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2420-2238T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499012 | ||||||
chr17:39499013
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2237T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499013 | ||||||
chr17:39499014
|
T | C | 13 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.2420-2236T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499014 | ||||||
chr17:39499015
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2235C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499015 | ||||||
chr17:39499016
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0003g0070 | 2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2234T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499016 | ||||||
chr17:39499018
|
T | C | 13 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.2420-2232T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499018 | ||||||
chr17:39499019
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2231C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499019 | ||||||
chr17:39499020
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2230T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499020 | ||||||
chr17:39499022
|
T | C | 9 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.2420-2228T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499022 | ||||||
chr17:39499023
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2227C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499023 | ||||||
chr17:39499023
|
CTTTCTTT others(112): Show |
C | 1 | a0001c0001t0003g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2420-2226_2420-210 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499023 | ||||||
chr17:39499024
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2226T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499024 | ||||||
chr17:39499025
|
TTC | T | 3 | a0001c0001t0003g0053a0001c0001t0007g0051a0001c0001t0008g0041 | 3 | HG00738.hp1 HG01346.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2420-2223_2420-222 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499025 | |||||
chr17:39499026
|
T | C | 5 | a0001c0001t0002g0042a0001c0001t0002g0059a0001c0001t0003g0050others(2): Show | 5 | HG00423.hp1 HG00597.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-2224T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499026 | ||||||
chr17:39499028
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0005g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2222T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499028 | ||||||
chr17:39499029
|
TTCTTTCT others(151): Show |
T | 1 | a0001c0001t0003g0031 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2420-2219_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499029 | |||||
chr17:39499030
|
T | C | 5 | a0001c0001t0002g0042a0001c0001t0002g0059a0001c0001t0003g0050others(2): Show | 5 | HG00423.hp1 HG00597.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-2220T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499030 | ||||||
chr17:39499031
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2219C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499031 | ||||||
chr17:39499032
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2218T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499032 | ||||||
chr17:39499034
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0003g0050a0001c0001t0058g0071 | 3 | HG00597.hp1 HG02040.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2216T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499034 | ||||||
chr17:39499035
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2215C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499035 | ||||||
chr17:39499035
|
CTTTCTTT others(168): Show |
C | 1 | a0001c0001t0007g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2420-2211_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499035 | |||||
chr17:39499036
|
T | C | 2 | a0001c0001t0002g0066a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2214T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499036 | ||||||
chr17:39499037
|
TTC | T | 3 | a0001c0001t0003g0053a0001c0001t0003g0069a0001c0001t0008g0041 | 3 | HG00738.hp1 HG01943.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2420-2211_2420-221 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499037 | |||||
chr17:39499038
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0003g0050a0001c0001t0058g0071 | 3 | HG00597.hp1 HG02040.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2212T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499038 | ||||||
chr17:39499039
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2211C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499039 | ||||||
chr17:39499039
|
CTTTCTTT others(180): Show |
C | 1 | a0001c0001t0005g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2420-2210_2420-202 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499039 | ||||||
chr17:39499040
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0005g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2210T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499040 | ||||||
chr17:39499041
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2209T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499041 | ||||||
chr17:39499042
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2208T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499042 | ||||||
chr17:39499043
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2207C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499043 | ||||||
chr17:39499044
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2206T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499044 | ||||||
chr17:39499046
|
T | C | 2 | a0001c0001t0002g0042a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2204T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499046 | ||||||
chr17:39499047
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0004g0030a0001c0002t0059g0012 | 3 | HG03491.hp2 HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2203C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499047 | ||||||
chr17:39499047
|
CTTTCTTT others(156): Show |
C | 2 | a0001c0001t0003g0053a0001c0001t0008g0041 | 2 | HG00738.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2420-2199_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499047 | |||||
chr17:39499047
|
CTTTCTTT others(172): Show |
C | 2 | a0001c0001t0005g0037a0001c0001t0028g0022 | 2 | NA18940.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2420-2202_2420-202 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499047 | ||||||
chr17:39499048
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0005g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2202T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499048 | ||||||
chr17:39499048
|
T | TTCCCTCC others(21): Show |
1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2201_2420-220 others(32): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499048 | |||||
chr17:39499049
|
TTC | T | 4 | a0001c0001t0003g0062a0001c0001t0003g0065a0001c0001t0003g0069others(1): Show | 4 | HG01943.hp1 HG01975.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2199_2420-219 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499049 | |||||
chr17:39499050
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2200T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499050 | ||||||
chr17:39499051
|
CTTTCTTT others(131): Show |
C | 1 | a0001c0001t0002g0058 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2420-2197_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499051 | |||||
chr17:39499052
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2198T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499052 | ||||||
chr17:39499054
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2196T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499054 | ||||||
chr17:39499055
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2195C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499055 | ||||||
chr17:39499056
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0066a0001c0002t0059g0012 | 3 | HG04204.hp2 NA19054.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2194T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499056 | ||||||
chr17:39499057
|
TTC | T | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0060others(3): Show | 6 | HG00423.hp1 HG02083.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.2420-2191_2420-219 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499057 | |||||
chr17:39499058
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2192T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499058 | ||||||
chr17:39499059
|
CTTTCTTT others(144): Show |
C | 1 | a0001c0001t0003g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2420-2187_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499059 | |||||
chr17:39499060
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2190T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499060 | ||||||
chr17:39499061
|
TTC | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0062a0001c0001t0003g0065others(1): Show | 4 | HG01975.hp2 HG02155.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2187_2420-218 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499061 | |||||
chr17:39499062
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2188T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499062 | ||||||
chr17:39499063
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2187C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499063 | ||||||
chr17:39499063
|
CTTTCTTT others(140): Show |
C | 1 | a0001c0001t0003g0047 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2420-2183_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499063 | |||||
chr17:39499064
|
T | C | 2 | a0001c0001t0002g0066a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2186T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499064 | ||||||
chr17:39499064
|
TTTCTTTC others(108): Show |
T | 1 | a0001c0001t0005g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2420-2183_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499064 | |||||
chr17:39499065
|
TTC | T | 3 | a0001c0001t0002g0059a0001c0001t0003g0070a0001c0001t0008g0054 | 3 | NA18966.hp1 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2420-2183_2420-218 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499065 | |||||
chr17:39499066
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2184T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499066 | ||||||
chr17:39499067
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2183C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499067 | ||||||
chr17:39499067
|
CTTTCTTT others(136): Show |
C | 2 | a0001c0001t0003g0055a0001c0001t0003g0060 | 2 | HG02523.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.2420-2179_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499067 | |||||
chr17:39499068
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2182T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499068 | ||||||
chr17:39499069
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2181T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499069 | ||||||
chr17:39499069
|
TTC | T | 4 | a0001c0001t0003g0057a0001c0001t0003g0063a0001c0001t0005g0032others(1): Show | 4 | HG00423.hp1 HG02083.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2179_2420-217 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499069 | |||||
chr17:39499070
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2180T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499070 | ||||||
chr17:39499071
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2179C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499071 | ||||||
chr17:39499071
|
CTTTCTTT others(111): Show |
C | 1 | a0001c0001t0003g0050 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2420-2177_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499071 | |||||
chr17:39499071
|
CTTTCTTT others(132): Show |
C | 3 | a0001c0001t0003g0062a0001c0001t0003g0065a0001c0001t0008g0064 | 3 | HG01975.hp2 HG02155.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2420-2175_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499071 | |||||
chr17:39499072
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2178T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499072 | ||||||
chr17:39499074
|
T | C | 2 | a0001c0001t0002g0042a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2176T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499074 | ||||||
chr17:39499075
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2175C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499075 | ||||||
chr17:39499075
|
CTTTCTTT others(107): Show |
C | 1 | a0001c0001t0058g0071 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2420-2173_2420-206 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499075 | |||||
chr17:39499076
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2174T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499076 | ||||||
chr17:39499077
|
TTC | T | 3 | a0001c0001t0002g0059a0001c0001t0003g0070a0001c0001t0008g0054 | 3 | NA18966.hp1 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2420-2171_2420-217 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499077 | |||||
chr17:39499078
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2172T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499078 | ||||||
chr17:39499079
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0002g0043a0001c0001t0004g0030 | 3 | HG00673.hp2 NA19060.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2420-2171C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499079 | ||||||
chr17:39499079
|
CTTTCTTT others(124): Show |
C | 4 | a0001c0001t0003g0057a0001c0001t0003g0063a0001c0001t0005g0032others(1): Show | 4 | HG00423.hp1 HG02083.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2167_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499079 | |||||
chr17:39499080
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0004g0030 | 2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2170T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499080 | ||||||
chr17:39499082
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2168T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499082 | ||||||
chr17:39499083
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2167C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499083 | ||||||
chr17:39499083
|
CTTTCTTT others(120): Show |
C | 1 | a0001c0001t0003g0049 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2420-2163_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499083 | |||||
chr17:39499083
|
CTTTCTTT others(136): Show |
C | 1 | a0001c0001t0005g0023 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2420-2166_2420-202 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499083 | ||||||
chr17:39499084
|
T | C | 2 | a0001c0001t0002g0066a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2166T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499084 | ||||||
chr17:39499086
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2164T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499086 | ||||||
chr17:39499087
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2163C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499087 | ||||||
chr17:39499087
|
CTTTCTTT others(116): Show |
C | 3 | a0001c0001t0002g0059a0001c0001t0003g0070a0001c0001t0008g0054 | 3 | NA18966.hp1 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2420-2159_2420-203 others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499087 | |||||
chr17:39499088
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2162T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499088 | ||||||
chr17:39499089
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2161T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499089 | ||||||
chr17:39499090
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2160T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499090 | ||||||
chr17:39499091
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2159C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499091 | ||||||
chr17:39499092
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2158T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499092 | ||||||
chr17:39499094
|
T | A | 1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2420-2156T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499094 | ||||||
chr17:39499094
|
T | C | 2 | a0001c0001t0002g0042a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2156T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499094 | ||||||
chr17:39499095
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2155C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499095 | ||||||
chr17:39499096
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2154T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499096 | ||||||
chr17:39499098
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2152T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499098 | ||||||
chr17:39499099
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2151C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499099 | ||||||
chr17:39499100
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2150T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499100 | ||||||
chr17:39499102
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2148T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499102 | ||||||
chr17:39499103
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2147C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499103 | ||||||
chr17:39499104
|
T | C | 2 | a0001c0001t0002g0066a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2146T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499104 | ||||||
chr17:39499105
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2145T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499105 | ||||||
chr17:39499106
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2144T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499106 | ||||||
chr17:39499107
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2143C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499107 | ||||||
chr17:39499108
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2142T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499108 | ||||||
chr17:39499109
|
T | C | 2 | a0001c0001t0002g0036a0001c0002t0059g0012 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2141T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499109 | ||||||
chr17:39499110
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2140T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499110 | ||||||
chr17:39499111
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2139C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499111 | ||||||
chr17:39499111
|
CTTTCTTT others(92): Show |
C | 1 | a0001c0001t0003g0068 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2420-2135_2420-203 others(103): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499111 | |||||
chr17:39499112
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2138T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499112 | ||||||
chr17:39499113
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2137T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499113 | ||||||
chr17:39499114
|
T | C | 2 | a0001c0001t0002g0042a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2136T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499114 | ||||||
chr17:39499115
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2135C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499115 | ||||||
chr17:39499116
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2134T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499116 | ||||||
chr17:39499117
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2133T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499117 | ||||||
chr17:39499118
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2132T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499118 | ||||||
chr17:39499120
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2130T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499120 | ||||||
chr17:39499121
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2129T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499121 | ||||||
chr17:39499122
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2128T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499122 | ||||||
chr17:39499123
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2127C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499123 | ||||||
chr17:39499124
|
T | C | 2 | a0001c0001t0002g0066a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2126T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499124 | ||||||
chr17:39499125
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2125T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499125 | ||||||
chr17:39499126
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2124T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499126 | ||||||
chr17:39499127
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2123C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499127 | ||||||
chr17:39499128
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2122T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499128 | ||||||
chr17:39499129
|
T | C | 2 | a0001c0001t0002g0036a0001c0002t0059g0012 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2121T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499129 | ||||||
chr17:39499130
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2120T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499130 | ||||||
chr17:39499131
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2119C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499131 | ||||||
chr17:39499132
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-2118T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499132 | ||||||
chr17:39499133
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2117T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499133 | ||||||
chr17:39499133
|
TTCTTTCT others(86): Show |
T | 1 | a0001c0001t0002g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2420-2116_2420-202 others(97): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499133 | ||||||
chr17:39499134
|
T | C | 2 | a0001c0001t0002g0042a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2420-2116T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499134 | ||||||
chr17:39499135
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2115C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499135 | ||||||
chr17:39499137
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2113T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499137 | ||||||
chr17:39499138
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2112T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499138 | ||||||
chr17:39499141
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2109T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499141 | ||||||
chr17:39499142
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2108T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499142 | ||||||
chr17:39499143
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2107C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499143 | ||||||
chr17:39499144
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2106T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499144 | ||||||
chr17:39499145
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2105T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499145 | ||||||
chr17:39499147
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2103C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499147 | ||||||
chr17:39499149
|
T | C | 2 | a0001c0001t0002g0036a0001c0002t0059g0012 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2101T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499149 | ||||||
chr17:39499150
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2100T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499150 | ||||||
chr17:39499151
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2099C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499151 | ||||||
chr17:39499153
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2097T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499153 | ||||||
chr17:39499154
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2096T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499154 | ||||||
chr17:39499155
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2095C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499155 | ||||||
chr17:39499157
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2093T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499157 | ||||||
chr17:39499158
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2420-2092T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499158 | ||||||
chr17:39499158
|
T | TTCTTTTC others(271): Show |
1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2092_2420-209 others(282): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499158 | ||||||
chr17:39499159
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2091C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499159 | ||||||
chr17:39499160
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2090T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499160 | ||||||
chr17:39499161
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2089T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499161 | ||||||
chr17:39499163
|
C | T | 2 | a0001c0001t0014g0159a0001c0002t0059g0012 | 2 | HG01255.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2087C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499163 | ||||||
chr17:39499164
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2086T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499164 | ||||||
chr17:39499165
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2085T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499165 | ||||||
chr17:39499167
|
C | T | 3 | a0001c0001t0004g0030a0001c0001t0014g0159a0001c0002t0059g0012 | 3 | HG01255.hp2 HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2083C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499167 | ||||||
chr17:39499169
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2081T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499169 | ||||||
chr17:39499169
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2081T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499169 | ||||||
chr17:39499171
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2079C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499171 | ||||||
chr17:39499172
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2078T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499172 | ||||||
chr17:39499173
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2077T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499173 | ||||||
chr17:39499174
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2076T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499174 | ||||||
chr17:39499175
|
C | T | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2075C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499175 | ||||||
chr17:39499176
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2074T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499176 | ||||||
chr17:39499177
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2073T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499177 | ||||||
chr17:39499179
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2420-2071C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499179 | ||||||
chr17:39499180
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2070T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499180 | ||||||
chr17:39499181
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2069T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499181 | ||||||
chr17:39499183
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2067C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499183 | ||||||
chr17:39499184
|
T | C | 2 | a0001c0001t0002g0043a0001c0002t0059g0012 | 2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2420-2066T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499184 | ||||||
chr17:39499185
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2420-2065T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499185 | ||||||
chr17:39499185
|
TTCTTTCT others(34): Show |
T | 1 | a0001c0001t0002g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2420-2064_2420-202 others(45): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499185 | ||||||
chr17:39499187
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0005g0033a0001c0002t0059g0012 | 3 | HG00673.hp2 HG02015.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2063C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499187 | ||||||
chr17:39499188
|
T | C | 3 | a0001c0001t0002g0034a0001c0001t0002g0043a0001c0001t0005g0033 | 3 | HG00673.hp2 HG02015.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2420-2062T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499188 | ||||||
chr17:39499189
|
T | G | 2 | a0001c0001t0002g0036a0001c0002t0059g0012 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2061T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499189 | ||||||
chr17:39499191
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0004g0030a0001c0001t0005g0033others(1): Show | 4 | HG00673.hp2 HG02015.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2420-2059C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499191 | ||||||
chr17:39499192
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2058T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499192 | ||||||
chr17:39499193
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0005g0033 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.2420-2057T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499193 | ||||||
chr17:39499193
|
TTC | T | 4 | a0001c0001t0007g0084a0001c0001t0027g0029a0001c0001t0027g0048others(1): Show | 4 | HG00140.hp1 HG01074.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2055_2420-205 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499193 | |||||
chr17:39499194
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2056T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499194 | ||||||
chr17:39499195
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0005g0033a0001c0002t0059g0012 | 3 | HG00673.hp2 HG02015.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2055C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499195 | ||||||
chr17:39499196
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2054T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499196 | ||||||
chr17:39499197
|
TTC | T | 5 | a0001c0001t0002g0058a0001c0001t0003g0031a0001c0001t0003g0050others(2): Show | 5 | HG00597.hp1 HG00621.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-2051_2420-205 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499197 | |||||
chr17:39499198
|
T | C | 5 | a0001c0001t0002g0034a0001c0001t0005g0033a0001c0001t0027g0029others(2): Show | 5 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-2052T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499198 | ||||||
chr17:39499199
|
C | T | 6 | a0001c0001t0002g0034a0001c0001t0004g0030a0001c0001t0005g0033others(3): Show | 6 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2051C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499199 | ||||||
chr17:39499200
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2050T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499200 | ||||||
chr17:39499201
|
TTCTTTCC others(18): Show |
T | 3 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083 | 3 | HG01123.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2420-2048_2420-202 others(29): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499201 | ||||||
chr17:39499203
|
C | T | 2 | a0001c0001t0002g0036a0001c0002t0059g0012 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2420-2047C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499203 | ||||||
chr17:39499204
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2420-2046T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499204 | ||||||
chr17:39499204
|
T | G | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2046T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499204 | ||||||
chr17:39499205
|
T | C | 5 | a0001c0001t0002g0018a0001c0001t0004g0014a0001c0001t0004g0016others(2): Show | 5 | HG02895.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2420-2045T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499205 | ||||||
chr17:39499205
|
T | TTCTTTCT others(55): Show |
1 | a0001c0001t0005g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2420-2043_2420-204 others(66): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499205 | |||||
chr17:39499206
|
TC | T | 7 | a0001c0001t0002g0018a0001c0001t0002g0042a0001c0001t0004g0014others(4): Show | 7 | HG02895.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420-2042delC | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499206 | |||||
chr17:39499207
|
C | CTTTCTTT others(142): Show |
1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2420-2043_2420-204 others(153): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499207 | ||||||
chr17:39499207
|
C | CTTTCTTT others(29): Show |
1 | a0001c0001t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2420-2043_2420-204 others(40): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499207 | ||||||
chr17:39499207
|
C | CTTTCTTT others(61): Show |
1 | a0001c0001t0004g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2420-2043_2420-204 others(72): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499207 | ||||||
chr17:39499207
|
C | T | 6 | a0001c0001t0002g0034a0001c0001t0004g0030a0001c0001t0005g0033others(3): Show | 6 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-2043C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499207 | ||||||
chr17:39499207
|
CCT | C | 4 | a0001c0001t0002g0058a0001c0001t0003g0031a0001c0001t0003g0050others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-2042_2420-204 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499207 | ||||||
chr17:39499208
|
C | T | 11 | a0001c0001t0002g0018a0001c0001t0002g0066a0001c0001t0004g0013others(8): Show | 11 | HG01255.hp2 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2420-2042C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499208 | ||||||
chr17:39499211
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-2039T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499211 | ||||||
chr17:39499212
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0005g0033a0001c0001t0007g0084 | 3 | HG02015.hp1 NA19054.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2420-2038T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499212 | ||||||
chr17:39499213
|
T | C | 1 | a0001c0001t0004g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2420-2037T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499213 | ||||||
chr17:39499214
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0066 | 2 | NA19054.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2420-2036T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499214 | ||||||
chr17:39499216
|
T | C | 18 | a0001c0001t0002g0042a0001c0001t0002g0066a0001c0001t0007g0084others(15): Show | 18 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.2420-2034T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499216 | ||||||
chr17:39499217
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0004g0030 | 2 | HG00673.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2033T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499217 | ||||||
chr17:39499220
|
T | C | 1 | a0001c0001t0007g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2420-2030T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499220 | ||||||
chr17:39499221
|
T | C | 2 | a0001c0001t0004g0030a0001c0002t0059g0012 | 2 | HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2029T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499221 | ||||||
chr17:39499222
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2420-2028T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499222 | ||||||
chr17:39499224
|
T | C | 1 | a0001c0001t0007g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2420-2026T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499224 | ||||||
chr17:39499224
|
TGA | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2420-2023_2420-202 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499224 | |||||
chr17:39499225
|
G | T | 15 | a0001c0001t0001g0125a0001c0001t0002g0018a0001c0001t0002g0019others(12): Show | 15 | HG00673.hp2 HG02109.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2420-2025G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499225 | ||||||
chr17:39499226
|
A | C | 3 | a0001c0001t0002g0034a0001c0001t0004g0030a0001c0002t0059g0012 | 3 | HG00673.hp2 HG04204.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2420-2024A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499226 | ||||||
chr17:39499226
|
A | T | 3 | a0001c0001t0002g0036a0001c0001t0004g0061a0001c0001t0007g0084 | 3 | HG03491.hp2 NA18995.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2420-2024A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499226 | ||||||
chr17:39499429
|
G | A | 1 | a0001c0001t0034g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2420-1821G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499429 | ||||||
chr17:39499461
|
G | T | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420-1789G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499461 | ||||||
chr17:39499504
|
C | T | 1 | a0002c0003t0016g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2420-1746C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499504 | ||||||
chr17:39499510
|
C | CT | 11 | a0001c0001t0002g0044a0001c0001t0008g0054a0001c0002t0021g0005others(8): Show | 11 | HG01884.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2420-1727dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39499510 | |||||
chr17:39499511
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2420-1739T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499511 | ||||||
chr17:39499803
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2420-1447C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39499803 | ||||||
chr17:39500058
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2420-1192G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39500058 | ||||||
chr17:39500140
|
G | T | 1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2420-1110G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39500140 | ||||||
chr17:39500408
|
G | A | 1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2420-842G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39500408 | ||||||
chr17:39500732
|
CT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2420-506delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39500732 | |||||
chr17:39500817
|
C | G | 1 | a0001c0001t0018g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2420-433C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39500817 | ||||||
chr17:39501207
|
C | CT | 68 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(65): Show | 69 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2420-33dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 39501207 | |||||
chr17:39501222
|
C | G | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2420-28C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 5/13 | chr17 | 39501222 | ||||||
chr17:39501924
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2609+485A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39501924 | ||||||
chr17:39501993
|
C | T | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2609+554C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39501993 | ||||||
chr17:39502213
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2609+774C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502213 | ||||||
chr17:39502252
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.2609+813G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502252 | ||||||
chr17:39502445
|
G | A | 1 | a0001c0001t0029g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2609+1006G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502445 | ||||||
chr17:39502501
|
T | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2609+1062T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502501 | ||||||
chr17:39502756
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2609+1317A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502756 | ||||||
chr17:39502809
|
A | G | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2609+1370A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502809 | ||||||
chr17:39502932
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2609+1493T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39502932 | ||||||
chr17:39503058
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2609+1619G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503058 | ||||||
chr17:39503117
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2609+1678G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503117 | ||||||
chr17:39503213
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2609+1774C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503213 | ||||||
chr17:39503353
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2609+1914G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503353 | ||||||
chr17:39503368
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2609+1929C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503368 | ||||||
chr17:39503377
|
G | A | 1 | a0001c0001t0010g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2609+1938G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503377 | ||||||
chr17:39503543
|
TGAG | T | 4 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0011g0105others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609+2108_2609+211 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39503543 | |||||
chr17:39503720
|
A | G | 1 | a0001c0001t0009g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2609+2281A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503720 | ||||||
chr17:39503729
|
G | A | 1 | a0002c0003t0016g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2609+2290G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39503729 | ||||||
chr17:39504058
|
C | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01071.hp1 HG01256.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2609+2619C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39504058 | ||||||
chr17:39504067
|
A | G | 1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2609+2628A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39504067 | ||||||
chr17:39504216
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2609+2777A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39504216 | ||||||
chr17:39504676
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0002g0042a0001c0001t0002g0066 | 3 | HG04115.hp2 NA19054.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2609+3237C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39504676 | ||||||
chr17:39504879
|
C | CA | 15 | a0001c0001t0002g0019a0001c0001t0002g0058a0001c0001t0002g0076others(12): Show | 15 | HG00140.hp1 HG00423.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.2609+3460dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39504879 | |||||
chr17:39504879
|
C | CAA | 16 | a0001c0001t0001g0178a0001c0001t0007g0075a0001c0001t0009g0087others(13): Show | 16 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609+3459_2609+346 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39504879 | |||||
chr17:39504879
|
C | CAAA | 27 | a0001c0001t0010g0091a0001c0001t0010g0106a0001c0001t0010g0107others(24): Show | 27 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2609+3458_2609+346 others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39504879 | |||||
chr17:39504879
|
C | CAAAA | 109 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0120others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.2609+3457_2609+346 others(8): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39504879 | |||||
chr17:39504879
|
C | CAAAAA | 34 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(31): Show | 35 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2609+3456_2609+346 others(9): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39504879 | |||||
chr17:39505045
|
A | G | 12 | a0001c0001t0003g0047a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG00423.hp1 HG00738.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609+3606A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505045 | ||||||
chr17:39505057
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2609+3618C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505057 | ||||||
chr17:39505227
|
C | CA | 13 | a0001c0001t0001g0206a0001c0001t0002g0038a0001c0001t0003g0052others(10): Show | 13 | HG00423.hp1 HG00597.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2609+3805dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39505227 | |||||
chr17:39505254
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2609+3815C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505254 | ||||||
chr17:39505265
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2609+3826A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505265 | ||||||
chr17:39505275
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2609+3836C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505275 | ||||||
chr17:39505329
|
A | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0034 | 2 | HG00673.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2609+3890A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505329 | ||||||
chr17:39505523
|
C | CA | 143 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0120others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2609+4104dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39505523 | |||||
chr17:39505523
|
C | CAA | 39 | a0001c0001t0001g0136a0001c0001t0001g0172a0001c0001t0001g0184others(36): Show | 39 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2609+4103_2609+410 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39505523 | |||||
chr17:39505808
|
G | C | 1 | a0001c0001t0007g0046 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2610-3897G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505808 | ||||||
chr17:39505914
|
A | G | 1 | a0001c0001t0010g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2610-3791A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505914 | ||||||
chr17:39505951
|
C | T | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2610-3754C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39505951 | ||||||
chr17:39506207
|
A | G | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2610-3498A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506207 | ||||||
chr17:39506212
|
A | AT | 64 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0169others(61): Show | 64 | HG00558.hp2 HG00673.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.2610-3471dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39506212 | |||||
chr17:39506212
|
A | ATT | 12 | a0001c0001t0002g0039a0001c0001t0003g0002a0001c0001t0004g0013others(9): Show | 12 | HG01361.hp2 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2610-3472_2610-347 others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39506212 | |||||
chr17:39506309
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0255 | 3 | HG01515.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2610-3396G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506309 | ||||||
chr17:39506460
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2610-3245C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506460 | ||||||
chr17:39506514
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2610-3191C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506514 | ||||||
chr17:39506679
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2610-3026T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506679 | ||||||
chr17:39506701
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2610-3004C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39506701 | ||||||
chr17:39507017
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2610-2688C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39507017 | ||||||
chr17:39507033
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0035 | 2 | HG01256.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.2610-2672A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39507033 | ||||||
chr17:39507315
|
G | A | 2 | a0001c0001t0001g0184a0001c0002t0059g0012 | 2 | HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2610-2390G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39507315 | ||||||
chr17:39507642
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0034 | 2 | HG00673.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2610-2063G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39507642 | ||||||
chr17:39508086
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2610-1619G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508086 | ||||||
chr17:39508102
|
C | T | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2610-1603C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508102 | ||||||
chr17:39508190
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2610-1515T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508190 | ||||||
chr17:39508202
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2610-1503C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508202 | ||||||
chr17:39508433
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2610-1272T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508433 | ||||||
chr17:39508464
|
A | C | 26 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0001t0002g0059others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2610-1241A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508464 | ||||||
chr17:39508540
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0230a0001c0001t0001g0234 | 3 | HG02559.hp2 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2610-1165A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508540 | ||||||
chr17:39508762
|
A | G | 1 | a0003c0005t0055g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2610-943A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39508762 | ||||||
chr17:39508997
|
C | CAA | 21 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(18): Show | 21 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.2610-691_2610-690d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39508997 | |||||
chr17:39508997
|
C | CAAA | 113 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0120others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.2610-692_2610-690d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39508997 | |||||
chr17:39508997
|
C | CAAAA | 50 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0184others(47): Show | 51 | HG00438.hp1 HG00438.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.2610-693_2610-690d others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 39508997 | |||||
chr17:39509044
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2610-661C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509044 | ||||||
chr17:39509301
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2610-404G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509301 | ||||||
chr17:39509318
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2610-387G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509318 | ||||||
chr17:39509337
|
T | C | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2610-368T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509337 | ||||||
chr17:39509435
|
T | G | 1 | a0005c0010t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2610-270T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509435 | ||||||
chr17:39509444
|
G | T | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2610-261G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 6/13 | chr17 | 39509444 | ||||||
chr17:39509778
|
A | C | 6 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2666+17A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39509778 | ||||||
chr17:39509875
|
G | A | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2666+114G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39509875 | ||||||
chr17:39509974
|
G | C | 1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2666+213G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39509974 | ||||||
chr17:39510069
|
C | G | 14 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01106.hp1 HG01123.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.2666+308C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510069 | ||||||
chr17:39510091
|
C | T | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2666+330C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510091 | ||||||
chr17:39510092
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2666+331G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510092 | ||||||
chr17:39510114
|
C | CT | 12 | a0001c0001t0001g0188a0001c0001t0001g0206a0001c0001t0001g0222others(9): Show | 12 | HG01109.hp1 HG01981.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2666+375dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39510114 | |||||
chr17:39510114
|
C | CTCT | 6 | a0001c0002t0021g0005a0001c0002t0023g0256a0001c0002t0023g0257others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+354_2666+355i others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39510114 | |||||
chr17:39510114
|
CT | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0158a0001c0001t0001g0195others(7): Show | 10 | HG01074.hp2 HG01256.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.2666+375delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39510114 | |||||
chr17:39510181
|
G | A | 2 | a0001c0001t0008g0077a0003c0005t0054g0252 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2666+420G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510181 | ||||||
chr17:39510448
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0244 | 2 | HG00558.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2666+687C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510448 | ||||||
chr17:39510594
|
CTCTCT | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2666+848_2666+852d others(7): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39510594 | |||||
chr17:39510882
|
G | A | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2667-647G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510882 | ||||||
chr17:39510893
|
G | A | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2667-636G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39510893 | ||||||
chr17:39511157
|
A | G | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2667-372A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39511157 | ||||||
chr17:39511210
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0007g0075 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2667-319G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39511210 | ||||||
chr17:39511214
|
C | CA | 7 | a0001c0001t0002g0019a0001c0001t0004g0013a0001c0001t0008g0041others(4): Show | 7 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2667-291dupA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39511214 | |||||
chr17:39511214
|
CA | C | 6 | a0001c0001t0001g0174a0001c0001t0002g0255a0001c0001t0003g0053others(3): Show | 6 | HG00738.hp1 HG01074.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2667-291delA | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39511214 | |||||
chr17:39511214
|
CAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2667-292_2667-291d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39511214 | |||||
chr17:39511214
|
CAAA | C | 7 | a0001c0001t0001g0147a0001c0001t0001g0210a0001c0001t0001g0221others(4): Show | 7 | HG01069.hp2 HG01192.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2667-293_2667-291d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 39511214 | |||||
chr17:39511449
|
T | C | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2667-80T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 7/13 | chr17 | 39511449 | ||||||
chr17:39512040
|
A | G | 1 | a0001c0001t0003g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2768+410A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512040 | ||||||
chr17:39512164
|
G | A | 2 | a0001c0002t0021g0005a0001c0002t0043g0006 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2768+534G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512164 | ||||||
chr17:39512235
|
G | A | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2768+605G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512235 | ||||||
chr17:39512284
|
T | G | 1 | a0001c0001t0033g0096 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2768+654T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512284 | ||||||
chr17:39512432
|
G | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0034 | 2 | HG00673.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2768+802G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512432 | ||||||
chr17:39512618
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2768+988C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512618 | ||||||
chr17:39512790
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2768+1160T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512790 | ||||||
chr17:39512803
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2768+1173C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39512803 | ||||||
chr17:39513283
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2768+1653T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39513283 | ||||||
chr17:39513360
|
G | A | 2 | a0001c0001t0010g0106a0001c0001t0010g0107 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2768+1730G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39513360 | ||||||
chr17:39513451
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2768+1821A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39513451 | ||||||
chr17:39513631
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2768+2001G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39513631 | ||||||
chr17:39513712
|
A | G | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2769-2019A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39513712 | ||||||
chr17:39514001
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2769-1730G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514001 | ||||||
chr17:39514094
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2769-1637C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514094 | ||||||
chr17:39514313
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2769-1418A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514313 | ||||||
chr17:39514488
|
G | T | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2769-1243G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514488 | ||||||
chr17:39514612
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2769-1119A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514612 | ||||||
chr17:39514678
|
G | A | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2769-1053G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514678 | ||||||
chr17:39514690
|
G | A | 1 | a0001c0001t0012g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2769-1041G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514690 | ||||||
chr17:39514741
|
A | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2769-990A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514741 | ||||||
chr17:39514819
|
A | T | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2769-912A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39514819 | ||||||
chr17:39515016
|
G | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2769-715G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515016 | ||||||
chr17:39515069
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2769-662C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515069 | ||||||
chr17:39515079
|
G | A | 1 | a0001c0001t0013g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2769-652G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515079 | ||||||
chr17:39515237
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2769-494A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515237 | ||||||
chr17:39515402
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2769-329T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515402 | ||||||
chr17:39515461
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2769-270G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515461 | ||||||
chr17:39515510
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2769-221C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515510 | ||||||
chr17:39515551
|
A | G | 3 | a0001c0001t0027g0029a0001c0001t0027g0048a0001c0001t0056g0067 | 3 | HG00140.hp1 HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2769-180A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515551 | ||||||
chr17:39515657
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2769-74G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 8/13 | chr17 | 39515657 | ||||||
chr17:39515852
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0138 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2846+44A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39515852 | ||||||
chr17:39515965
|
G | T | 8 | a0001c0002t0021g0005a0001c0002t0023g0256a0001c0002t0023g0257others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2846+157G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39515965 | ||||||
chr17:39516071
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2846+263C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39516071 | ||||||
chr17:39516383
|
G | GTC | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2846+578_2846+579d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 39516383 | |||||
chr17:39516467
|
CCACCTTA others(22): Show |
C | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2846+665_2846+693d others(31): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 39516467 | |||||
chr17:39516660
|
C | CT | 13 | a0001c0001t0001g0001a0001c0001t0001g0206a0001c0001t0001g0215others(10): Show | 14 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2847-760dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 39516660 | |||||
chr17:39516660
|
CT | C | 10 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0241others(7): Show | 10 | HG01070.hp2 HG01109.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.2847-760delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 39516660 | |||||
chr17:39516731
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2847-709T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39516731 | ||||||
chr17:39516866
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0035 | 2 | HG01256.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.2847-574T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39516866 | ||||||
chr17:39516915
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0160 | 3 | NA18993.hp1 NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2847-525G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39516915 | ||||||
chr17:39516928
|
G | T | 4 | a0001c0002t0023g0256a0001c0002t0023g0257a0001c0002t0025g0258others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2847-512G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39516928 | ||||||
chr17:39517089
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2847-351A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 9/13 | chr17 | 39517089 | ||||||
chr17:39517667
|
T | A | 17 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(14): Show | 17 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2963+111T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39517667 | ||||||
chr17:39517689
|
G | A | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2963+133G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39517689 | ||||||
chr17:39517793
|
A | G | 1 | a0001c0001t0007g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2963+237A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39517793 | ||||||
chr17:39517808
|
T | C | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2963+252T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39517808 | ||||||
chr17:39517928
|
C | T | 1 | a0001c0002t0049g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2963+372C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39517928 | ||||||
chr17:39518137
|
C | T | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2963+581C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518137 | ||||||
chr17:39518285
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2963+729G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518285 | ||||||
chr17:39518313
|
C | T | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2963+757C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518313 | ||||||
chr17:39518315
|
C | T | 66 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0120others(63): Show | 66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2963+759C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518315 | ||||||
chr17:39518323
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2963+767C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518323 | ||||||
chr17:39518323
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2963+767C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518323 | ||||||
chr17:39518430
|
T | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2963+874T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518430 | ||||||
chr17:39518473
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2963+917C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518473 | ||||||
chr17:39518474
|
G | A | 10 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.2963+918G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518474 | ||||||
chr17:39518661
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2963+1105G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518661 | ||||||
chr17:39518749
|
G | C | 1 | a0005c0010t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2963+1193G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39518749 | ||||||
chr17:39519150
|
G | A | 14 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01106.hp1 HG01123.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.2964-806G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519150 | ||||||
chr17:39519198
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2964-758C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519198 | ||||||
chr17:39519298
|
C | CT | 11 | a0001c0001t0002g0058a0001c0001t0003g0052a0001c0001t0003g0078others(8): Show | 11 | HG00597.hp1 HG00621.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.2964-631dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519298 | |||||
chr17:39519298
|
C | CTTT | 5 | a0001c0002t0021g0021a0001c0002t0023g0256a0001c0002t0023g0257others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2964-633_2964-631d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519298 | |||||
chr17:39519298
|
C | CTTTT | 5 | a0001c0002t0021g0005a0001c0002t0025g0258a0001c0002t0043g0006others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2964-634_2964-631d others(6): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519298 | |||||
chr17:39519298
|
CT | C | 25 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.2964-631delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519298 | |||||
chr17:39519298
|
CTT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0120others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2964-632_2964-631d others(4): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519298 | |||||
chr17:39519342
|
G | A | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2964-614G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519342 | ||||||
chr17:39519447
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2964-509G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519447 | ||||||
chr17:39519527
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2964-429C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519527 | ||||||
chr17:39519585
|
C | CT | 5 | a0001c0001t0001g0220a0001c0001t0003g0049a0001c0001t0007g0046others(2): Show | 5 | HG00140.hp2 HG02976.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2964-354dupT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519585 | |||||
chr17:39519585
|
CT | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0125a0001c0001t0001g0212others(10): Show | 13 | HG00738.hp1 HG01070.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.2964-354delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 39519585 | |||||
chr17:39519602
|
T | A | 2 | a0001c0001t0014g0130a0001c0002t0021g0021 | 2 | HG02004.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2964-354T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519602 | ||||||
chr17:39519603
|
A | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0051g0187 | 3 | HG00673.hp1 NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2964-353A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 10/13 | chr17 | 39519603 | ||||||
chr17:39520256
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0048g0189 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3095+169A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520256 | ||||||
chr17:39520420
|
G | A | 1 | a0001c0001t0024g0254 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3095+333G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520420 | ||||||
chr17:39520434
|
C | T | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3095+347C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520434 | ||||||
chr17:39520516
|
G | A | 12 | a0001c0001t0010g0091a0001c0001t0011g0103a0001c0001t0011g0104others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3095+429G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520516 | ||||||
chr17:39520691
|
T | TTTG | 142 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.3095+628_3095+630d others(5): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 39520691 | |||||
chr17:39520691
|
T | TTTGTTGT others(5): Show |
1 | a0001c0002t0042g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3095+619_3095+630d others(14): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 39520691 | |||||
chr17:39520691
|
T | TTTGTTGT others(8): Show |
1 | a0001c0002t0021g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3095+616_3095+630d others(17): Show |
CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 39520691 | |||||
chr17:39520801
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3095+714C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520801 | ||||||
chr17:39520821
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.3095+734C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520821 | ||||||
chr17:39520868
|
A | G | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3095+781A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39520868 | ||||||
chr17:39521076
|
C | G | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3095+989C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521076 | ||||||
chr17:39521206
|
C | T | 1 | a0001c0001t0018g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3095+1119C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521206 | ||||||
chr17:39521292
|
C | T | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3095+1205C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521292 | ||||||
chr17:39521293
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3095+1206G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521293 | ||||||
chr17:39521307
|
C | T | 1 | a0001c0001t0057g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3095+1220C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521307 | ||||||
chr17:39521411
|
C | T | 6 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0018g0086others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.3095+1324C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521411 | ||||||
chr17:39521412
|
G | A | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3095+1325G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521412 | ||||||
chr17:39521431
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3095+1344T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521431 | ||||||
chr17:39521464
|
C | T | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3095+1377C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521464 | ||||||
chr17:39521621
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3095+1534G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521621 | ||||||
chr17:39521861
|
CT | C | 26 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(23): Show | 26 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3095+1789delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 39521861 | |||||
chr17:39521896
|
C | G | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3095+1809C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39521896 | ||||||
chr17:39522103
|
G | T | 1 | a0002c0003t0016g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3095+2016G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522103 | ||||||
chr17:39522158
|
G | T | 1 | a0001c0001t0002g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3095+2071G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522158 | ||||||
chr17:39522322
|
G | C | 1 | a0001c0001t0007g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3095+2235G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522322 | ||||||
chr17:39522335
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3095+2248C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522335 | ||||||
chr17:39522338
|
C | T | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3095+2251C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522338 | ||||||
chr17:39522509
|
A | C | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3096-2165A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522509 | ||||||
chr17:39522526
|
C | A | 14 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3096-2148C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522526 | ||||||
chr17:39522686
|
G | T | 2 | a0001c0001t0003g0063a0001c0001t0008g0064 | 2 | HG02083.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.3096-1988G>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522686 | ||||||
chr17:39522700
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0035 | 2 | HG01256.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.3096-1974C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522700 | ||||||
chr17:39522805
|
C | G | 4 | a0001c0001t0002g0076a0001c0001t0003g0078a0001c0001t0007g0075others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3096-1869C>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522805 | ||||||
chr17:39522818
|
C | T | 31 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(28): Show | 31 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.3096-1856C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39522818 | ||||||
chr17:39523001
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3096-1673C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39523001 | ||||||
chr17:39523042
|
T | C | 1 | a0001c0001t0008g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3096-1632T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39523042 | ||||||
chr17:39523238
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3096-1436C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39523238 | ||||||
chr17:39523723
|
G | A | 1 | a0001c0002t0059g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3096-951G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39523723 | ||||||
chr17:39523843
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3096-831C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39523843 | ||||||
chr17:39524003
|
A | T | 4 | a0001c0001t0002g0076a0001c0001t0003g0078a0001c0001t0007g0075others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3096-671A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39524003 | ||||||
chr17:39524050
|
T | C | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3096-624T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39524050 | ||||||
chr17:39524338
|
A | C | 1 | a0001c0002t0049g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3096-336A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39524338 | ||||||
chr17:39524429
|
T | C | 1 | a0007c0006t0019g0007 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3096-245T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 11/13 | chr17 | 39524429 | ||||||
chr17:39525079
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3307+194C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525079 | ||||||
chr17:39525434
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3308-430T>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525434 | ||||||
chr17:39525564
|
C | T | 1 | a0001c0002t0043g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3308-300C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525564 | ||||||
chr17:39525690
|
C | T | 1 | a0001c0001t0008g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3308-174C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525690 | ||||||
chr17:39525748
|
C | T | 34 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(31): Show | 34 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.3308-116C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525748 | ||||||
chr17:39525838
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0048g0189 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3308-26A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 12/13 | chr17 | 39525838 | ||||||
chr17:39526404
|
A | G | 34 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(31): Show | 34 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.3760+88A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39526404 | ||||||
chr17:39526649
|
A | G | 15 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(12): Show | 15 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.3760+333A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39526649 | ||||||
chr17:39526900
|
T | C | 34 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(31): Show | 34 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.3760+584T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39526900 | ||||||
chr17:39526975
|
A | T | 17 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(14): Show | 17 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.3760+659A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39526975 | ||||||
chr17:39526978
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3760+662C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39526978 | ||||||
chr17:39527001
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0181 | 2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.3760+685G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527001 | ||||||
chr17:39527295
|
A | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3760+979A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527295 | ||||||
chr17:39527312
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3760+996T>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527312 | ||||||
chr17:39527411
|
G | A | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0015g0101 | 3 | HG02145.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3760+1095G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527411 | ||||||
chr17:39527551
|
A | G | 1 | a0001c0001t0004g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3760+1235A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527551 | ||||||
chr17:39527584
|
A | G | 1 | a0001c0001t0030g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3760+1268A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527584 | ||||||
chr17:39527726
|
T | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02015.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.3760+1410T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527726 | ||||||
chr17:39527735
|
C | T | 2 | a0003c0005t0054g0252a0003c0005t0055g0251 | 2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3760+1419C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527735 | ||||||
chr17:39527758
|
G | C | 1 | a0001c0001t0029g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3760+1442G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527758 | ||||||
chr17:39527783
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3760+1467G>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39527783 | ||||||
chr17:39528154
|
T | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.3760+1838T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528154 | ||||||
chr17:39528247
|
A | T | 19 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(16): Show | 19 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3760+1931A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528247 | ||||||
chr17:39528263
|
T | A | 6 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG00741.hp1 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3760+1947T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528263 | ||||||
chr17:39528370
|
G | C | 8 | a0001c0001t0010g0091a0001c0001t0012g0095a0001c0001t0012g0115others(5): Show | 8 | HG02129.hp2 HG02132.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.3760+2054G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528370 | ||||||
chr17:39528523
|
C | T | 4 | a0001c0002t0019g0009a0001c0002t0020g0008a0001c0002t0020g0011others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3761-2081C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528523 | ||||||
chr17:39528557
|
A | C | 1 | a0004c0004t0017g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3761-2047A>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528557 | ||||||
chr17:39528672
|
T | A | 2 | a0001c0002t0021g0021a0001c0002t0042g0020 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3761-1932T>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528672 | ||||||
chr17:39528737
|
C | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3761-1867C>A | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39528737 | ||||||
chr17:39529141
|
G | C | 2 | a0001c0002t0021g0005a0001c0002t0043g0006 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3761-1463G>C | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39529141 | ||||||
chr17:39529148
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.3761-1456A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39529148 | ||||||
chr17:39529438
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3761-1166A>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39529438 | ||||||
chr17:39529862
|
AT | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0035others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3761-733delT | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 39529862 | |||||
chr17:39530125
|
A | G | 12 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0108others(9): Show | 12 | HG02055.hp1 HG02280.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.3761-479A>G | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39530125 | ||||||
chr17:39530421
|
C | T | 3 | a0002c0003t0016g0117a0002c0003t0016g0118a0002c0003t0016g0119 | 3 | HG02055.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3761-183C>T | CDK12 | ENSG00000167258.16 | transcript | ENST00000447079.6 | protein_coding | 13/13 | chr17 | 39530421 |