geneid | 11200 |
---|---|
ensemblid | ENSG00000183765.24 |
hgncid | 16627 |
symbol | CHEK2 |
name | checkpoint kinase 2 |
refseq_nuc | NM_007194.4 |
refseq_prot | NP_009125.1 |
ensembl_nuc | ENST00000404276.6 |
ensembl_prot | ENSP00000385747.1 |
mane_status | MANE Select |
chr | chr22 |
start | 28687743 |
end | 28741820 |
strand | - |
ver | v1.2 |
region | chr22:28687743-28741820 |
region5000 | chr22:28682743-28746820 |
regionname0 | CHEK2_chr22_28687743_28741820 |
regionname5000 | CHEK2_chr22_28682743_28746820 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 543 | 377 | 85 | 67 | 166 | 15 | 42 | 121 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0002 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0003 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0004 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0005 | 0/0 | 543 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0006 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0007 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0008 | 0/0 | 543 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1632 | 360 | 80 | 67 | 155 | 15 | 41 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0002 | 0/0 | 1632 | 14 | 5 | 0 | 8 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0003 | 0/0 | 1632 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0004 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0005 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0006 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0007 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0008 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0009 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0010 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
c0011 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 213 | 381 | 86 | 67 | 168 | 16 | 42 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
t0002 | 0/0 | 213 | 2 | 2 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
t0003 | 0/0 | 213 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0351 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1632 | 360 | 80 | 67 | 155 | 15 | 41 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0002 | 0/0 | 1632 | 14 | 5 | 0 | 8 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0003 | 0/0 | 1632 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0004 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0002c0011 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0003c0007 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0004c0008 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0005c0009 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0006c0006 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0007c0010 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0008c0005 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1844 | 359 | 80 | 66 | 155 | 15 | 41 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0001t0003 | 0/0 | 1844 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0002t0001 | 0/0 | 1844 | 12 | 3 | 0 | 8 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0002t0002 | 0/0 | 1844 | 2 | 2 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0003t0001 | 0/0 | 1844 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0001c0004t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0002c0011t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0003c0007t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0004c0008t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0005c0009t0001 | 0/0 | 1844 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0006c0006t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0007c0010t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
a0008c0005t0001 | 0/0 | 1844 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | copy fasta | chr22 | 28682743 | 28746820 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0351 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0002t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0002c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0003c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0004c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0005c0009t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0006c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0007c0010t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
a0008c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00323 | hp1 | a0008 | c0005 | t0001 | g0220 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00621 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0370 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0380 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01978 | hp1 | a0005 | c0009 | t0001 | g0293 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02132 | hp1 | a0003 | c0007 | t0001 | g0297 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0344 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02818 | hp2 | a0006 | c0006 | t0001 | g0137 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03130 | hp2 | a0002 | c0011 | t0001 | g0038 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0379 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03540 | hp2 | a0007 | c0010 | t0001 | g0375 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18959 | hp2 | a0004 | c0008 | t0001 | g0150 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0367 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | GIH | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0351 | REF | REF | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:28687932
|
T | C | 1 | a0003 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1597A>G | p.Thr533Ala | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 1655/1844 | 1597/1632 | 533/543 | chr22 | 28687932 | ||
chr22:28687968
|
G | A | 1 | a0004 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.1561C>T | p.Arg521Trp | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 1619/1844 | 1561/1632 | 521/543 | chr22 | 28687968 | ||
chr22:28689187
|
T | C | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1490A>G | p.Asp497Gly | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/15 | 1548/1844 | 1490/1632 | 497/543 | chr22 | 28689187 | ||
chr22:28695159
|
A | C | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1343T>G | p.Ile448Ser | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/15 | 1401/1844 | 1343/1632 | 448/543 | chr22 | 28695159 | ||
chr22:28695839
|
T | C | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1130A>G | p.Glu377Gly | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/15 | 1188/1844 | 1130/1632 | 377/543 | chr22 | 28695839 | ||
chr22:28725099
|
A | G | 1 | a0008 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.470T>C | p.Ile157Thr | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/15 | 528/1844 | 470/1632 | 157/543 | chr22 | 28725099 | ||
chr22:28734468
|
G | A | 1 | a0002 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.254C>T | p.Pro85Leu | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 312/1844 | 254/1632 | 85/543 | chr22 | 28734468 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:28695766
|
A | G | 1 | a0001c0003 | 2 | NA18962.hp2 NA18968.hp1 |
synonymous_variant | LOW | c.1203T>C | p.Thr401Thr | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/15 | 1261/1844 | 1203/1632 | 401/543 | chr22 | 28695766 | ||
chr22:28734470
|
T | C | 1 | a0001c0002 | 14 | HG00438.hp2 HG00673.hp1 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.252A>G | p.Glu84Glu | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 310/1844 | 252/1632 | 84/543 | chr22 | 28734470 | ||
chr22:28734707
|
C | T | 1 | a0001c0004 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.15G>A | p.Ser5Ser | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 73/1844 | 15/1632 | 5/543 | chr22 | 28734707 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:28687868
|
A | G | 1 | a0001c0001t0003 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 29 | chr22 | 28687868 | |||||
chr22:28741802
|
C | A | 1 | a0001c0002t0002 | 2 | HG01891.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-40G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/15 | 7081 | chr22 | 28741802 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:28688154
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1543-168G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688154 | ||||||
chr22:28688178
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0346others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-192A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688178 | ||||||
chr22:28688354
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0047 | 3 | HG02258.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1543-368A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688354 | ||||||
chr22:28688397
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0058others(21): Show | 24 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1543-411C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688397 | ||||||
chr22:28688606
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0143a0001c0001t0001g0329others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+529A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688606 | ||||||
chr22:28688817
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1542+318A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688817 | ||||||
chr22:28688859
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1542+276A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688859 | ||||||
chr22:28688972
|
C | G | 1 | a0001c0001t0001g0358 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1542+163G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688972 | ||||||
chr22:28689124
|
A | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0027others(1): Show | 6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+11T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28689124 | ||||||
chr22:28689352
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1462-137T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689352 | ||||||
chr22:28689413
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1462-198C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689413 | ||||||
chr22:28689426
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0334 | 2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1462-211A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689426 | ||||||
chr22:28689654
|
A | G | 6 | a0001c0001t0001g0147a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | NA18939.hp1 NA18955.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462-439T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689654 | ||||||
chr22:28689713
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-498G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689713 | ||||||
chr22:28689714
|
A | T | 1 | a0001c0001t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-499T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689714 | ||||||
chr22:28689715
|
C | CTGGATAC others(3): Show |
1 | a0001c0001t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-501_1462-500i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689715 | ||||||
chr22:28689716
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-501T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689716 | ||||||
chr22:28689804
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-589C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689804 | ||||||
chr22:28689822
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-607T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689822 | ||||||
chr22:28690103
|
C | G | 9 | a0001c0001t0001g0273a0001c0002t0001g0363a0001c0002t0001g0364others(6): Show | 9 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.1462-888G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690103 | ||||||
chr22:28690105
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(193): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1462-890G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690105 | ||||||
chr22:28690141
|
A | G | 2 | a0001c0001t0001g0346a0001c0001t0001g0362 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1462-926T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690141 | ||||||
chr22:28690214
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1462-999C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690214 | ||||||
chr22:28690309
|
T | C | 2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1462-1094A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690309 | ||||||
chr22:28690320
|
C | T | 2 | a0001c0001t0001g0275a0001c0001t0001g0278 | 2 | NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1462-1105G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690320 | ||||||
chr22:28690366
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1151G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690366 | ||||||
chr22:28690542
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0143 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1462-1327G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690542 | ||||||
chr22:28690560
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0143a0001c0001t0001g0329others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1345C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690560 | ||||||
chr22:28690628
|
C | CA | 11 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0001g0163others(8): Show | 11 | HG00438.hp1 HG01346.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-1414dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690628 | ||||||
chr22:28690628
|
CAA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1415_1462-141 others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690628 | ||||||
chr22:28690857
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1462-1642C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690857 | ||||||
chr22:28690947
|
C | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0143a0001c0001t0001g0329others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1732G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690947 | ||||||
chr22:28690952
|
TG | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1738delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690952 | ||||||
chr22:28691053
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1462-1838A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691053 | ||||||
chr22:28691108
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1462-1893A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691108 | ||||||
chr22:28691145
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1462-1930G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691145 | ||||||
chr22:28691154
|
G | C | 58 | a0001c0001t0001g0010a0001c0001t0001g0084a0001c0001t0001g0087others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1462-1939C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691154 | ||||||
chr22:28691257
|
A | C | 1 | a0001c0001t0001g0303 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1462-2042T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691257 | ||||||
chr22:28691294
|
ACATGGTG others(873): Show |
A | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1461+1858_1462-208 others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691294 | ||||||
chr22:28691434
|
C | T | 12 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1462-2219G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691434 | ||||||
chr22:28691458
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-2243T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691458 | ||||||
chr22:28691460
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1462-2245T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691460 | ||||||
chr22:28691545
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1462-2330T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691545 | ||||||
chr22:28691598
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1462-2383T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691598 | ||||||
chr22:28691830
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1461+2202C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691830 | ||||||
chr22:28691841
|
G | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1461+2191C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691841 | ||||||
chr22:28692095
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0239 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1461+1937T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692095 | ||||||
chr22:28692135
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1461+1897A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692135 | ||||||
chr22:28692136
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1461+1896C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692136 | ||||||
chr22:28692350
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1461+1682G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692350 | ||||||
chr22:28692463
|
A | G | 11 | a0001c0001t0001g0144a0001c0001t0001g0273a0001c0002t0001g0006others(8): Show | 11 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1461+1569T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692463 | ||||||
chr22:28692471
|
T | TTTTG | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1461+1557_1461+156 others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692471 | ||||||
chr22:28692471
|
T | TTTTGTTT others(5): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0027others(1): Show | 6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+1549_1461+156 others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692471 | ||||||
chr22:28692602
|
C | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1461+1430G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692602 | ||||||
chr22:28692831
|
C | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1461+1201G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692831 | ||||||
chr22:28692851
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0197 | 2 | NA18946.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1461+1181A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692851 | ||||||
chr22:28692914
|
C | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1461+1118G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692914 | ||||||
chr22:28693107
|
C | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1461+925G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693107 | ||||||
chr22:28693249
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0027others(1): Show | 6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+783C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693249 | ||||||
chr22:28693784
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1461+248C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693784 | ||||||
chr22:28693858
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0334 | 2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1461+174G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693858 | ||||||
chr22:28694375
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1376-258C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694375 | ||||||
chr22:28694493
|
G | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1376-376C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694493 | ||||||
chr22:28694780
|
A | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1375+347T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694780 | ||||||
chr22:28694849
|
T | G | 1 | a0001c0002t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1375+278A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694849 | ||||||
chr22:28694902
|
G | A | 34 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(31): Show | 34 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1375+225C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694902 | ||||||
chr22:28694955
|
T | C | 1 | a0001c0001t0001g0356 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1375+172A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694955 | ||||||
chr22:28694973
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1375+154T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694973 | ||||||
chr22:28694987
|
C | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0169a0001c0001t0001g0183others(7): Show | 11 | HG02015.hp1 HG02056.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1375+140G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694987 | ||||||
chr22:28695049
|
G | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1375+78C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28695049 | ||||||
chr22:28695333
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1260-91T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/14 | chr22 | 28695333 | ||||||
chr22:28695384
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1260-142G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/14 | chr22 | 28695384 | ||||||
chr22:28696087
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1096-214G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696087 | ||||||
chr22:28696141
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0031 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-268A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696141 | ||||||
chr22:28696189
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1096-316T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696189 | ||||||
chr22:28696193
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0123a0001c0001t0001g0124others(38): Show | 41 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1096-320G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696193 | ||||||
chr22:28696247
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096-374T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696247 | ||||||
chr22:28696267
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1096-394G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696267 | ||||||
chr22:28696400
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1095+501C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696400 | ||||||
chr22:28696604
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1095+297G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696604 | ||||||
chr22:28696651
|
A | G | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1095+250T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696651 | ||||||
chr22:28696713
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1095+188G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696713 | ||||||
chr22:28696732
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 20 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1095+169G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696732 | ||||||
chr22:28696738
|
C | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0295a0001c0001t0001g0298others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+163G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696738 | ||||||
chr22:28697204
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1009-217G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697204 | ||||||
chr22:28697251
|
A | G | 375 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(372): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1009-264T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697251 | ||||||
chr22:28697290
|
T | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 20 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1009-303A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697290 | ||||||
chr22:28697572
|
CT | C | 8 | a0001c0001t0001g0147a0001c0001t0001g0230a0001c0001t0001g0242others(5): Show | 8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009-586delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697572 | ||||||
chr22:28697574
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1009-587A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697574 | ||||||
chr22:28697765
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1009-778C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697765 | ||||||
chr22:28697978
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1009-991C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697978 | ||||||
chr22:28698096
|
T | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1009-1109A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698096 | ||||||
chr22:28698228
|
T | TA | 45 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022others(42): Show | 46 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1009-1242dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(1): Show |
88 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0123others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1009-1249_1009-124 others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(2): Show |
17 | a0001c0001t0001g0100a0001c0001t0001g0125a0001c0001t0001g0127others(14): Show | 17 | HG01175.hp2 HG01243.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1009-1250_1009-124 others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0334 | 2 | HG01891.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1009-1251_1009-124 others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0189 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1009-1254_1009-124 others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(7): Show |
65 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.1009-1255_1009-124 others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(8): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(36): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1009-1256_1009-124 others(19): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0001t0001g0196others(1): Show | 4 | HG01981.hp2 HG02056.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1257_1009-124 others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1009-1258_1009-124 others(21): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0348 | 2 | HG00735.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1009-1260_1009-124 others(23): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(20): Show |
1 | a0001c0002t0001g0367 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1009-1242_1009-124 others(31): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(21): Show |
7 | a0001c0002t0001g0006a0001c0002t0001g0363a0001c0002t0001g0364others(4): Show | 7 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-1242_1009-124 others(32): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698228
|
T | TAAAAAAA others(26): Show |
1 | a0001c0002t0001g0366 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1009-1242_1009-124 others(37): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | ||||||
chr22:28698322
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1009-1335C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698322 | ||||||
chr22:28698356
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-1369A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698356 | ||||||
chr22:28698364
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1009-1377G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698364 | ||||||
chr22:28698374
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0246a0001c0001t0001g0268others(1): Show | 4 | HG02886.hp2 HG02896.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1387C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698374 | ||||||
chr22:28698388
|
T | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0100others(107): Show | 110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1009-1401A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698388 | ||||||
chr22:28698499
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1008+1339A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698499 | ||||||
chr22:28698768
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1008+1070G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698768 | ||||||
chr22:28698770
|
G | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG02027.hp1 HG02165.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1068C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698770 | ||||||
chr22:28698786
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1008+1052G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698786 | ||||||
chr22:28698791
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0136 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1008+1047T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698791 | ||||||
chr22:28698840
|
A | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0061others(84): Show | 88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1008+998T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698840 | ||||||
chr22:28699362
|
C | CT | 77 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0042others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1008+475dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | ||||||
chr22:28699362
|
CT | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1008+475delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | ||||||
chr22:28699362
|
CTT | C | 18 | a0001c0001t0001g0061a0001c0001t0001g0105a0001c0001t0001g0152others(15): Show | 18 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008+474_1008+475d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | ||||||
chr22:28699365
|
T | TTC | 15 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022others(12): Show | 16 | HG01192.hp1 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008+472_1008+473i others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699365 | ||||||
chr22:28699370
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022others(12): Show | 16 | HG01192.hp1 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008+468A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699370 | ||||||
chr22:28699397
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1008+441G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699397 | ||||||
chr22:28699489
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0334 | 2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+349G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699489 | ||||||
chr22:28699492
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0334 | 2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+346C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699492 | ||||||
chr22:28699502
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0334 | 2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+336G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699502 | ||||||
chr22:28699646
|
AC | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0100others(107): Show | 110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1008+191delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699646 | ||||||
chr22:28699654
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1008+184C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699654 | ||||||
chr22:28699669
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1008+169C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699669 | ||||||
chr22:28699694
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1008+144T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699694 | ||||||
chr22:28699830
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19088.hp1 | splice_region_variant&intron_variant | LOW | c.1008+8A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699830 | ||||||
chr22:28699998
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0093 | 2 | NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.909-61T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28699998 | ||||||
chr22:28700211
|
C | CT | 21 | a0001c0001t0001g0063a0001c0001t0001g0099a0001c0001t0001g0118others(18): Show | 21 | HG00438.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.909-275dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700211 | ||||||
chr22:28700373
|
G | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.909-436C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700373 | ||||||
chr22:28700547
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.909-610A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700547 | ||||||
chr22:28700701
|
C | T | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.909-764G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700701 | ||||||
chr22:28700705
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.909-768G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700705 | ||||||
chr22:28700786
|
C | CTTTA | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(2): Show | 5 | HG00408.hp1 HG02083.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-853_909-850dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700786 | ||||||
chr22:28700853
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.909-916T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700853 | ||||||
chr22:28701029
|
T | A | 12 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1092A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701029 | ||||||
chr22:28701192
|
T | TGTGATCA others(3): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.909-1265_909-1256d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701192 | ||||||
chr22:28701289
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.909-1352G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701289 | ||||||
chr22:28701314
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.909-1377C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701314 | ||||||
chr22:28701618
|
T | C | 1 | a0001c0001t0001g0360 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.909-1681A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701618 | ||||||
chr22:28701785
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0165 | 2 | NA18747.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.908+1720C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701785 | ||||||
chr22:28701954
|
A | AT | 200 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.908+1550dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701954 | ||||||
chr22:28701954
|
A | ATT | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(64): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.908+1549_908+1550d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701954 | ||||||
chr22:28702135
|
C | CTG | 10 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0164others(7): Show | 10 | HG00323.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+1368_908+1369d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTG | 31 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0084others(28): Show | 31 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.908+1366_908+1369d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTG | 30 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0049others(27): Show | 31 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.908+1364_908+1369d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(1): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(33): Show | 36 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.908+1362_908+1369d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(3): Show |
74 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0105others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.908+1360_908+1369d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(5): Show |
33 | a0001c0001t0001g0106a0001c0001t0001g0124a0001c0001t0001g0125others(30): Show | 33 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.908+1358_908+1369d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(7): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0168others(11): Show | 15 | HG01074.hp2 HG01243.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.908+1356_908+1369d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0123a0001c0001t0001g0172others(3): Show | 6 | HG02735.hp1 HG03654.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1354_908+1369d others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(11): Show |
3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0201 | 3 | HG02155.hp2 HG02523.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.908+1352_908+1369d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.908+1350_908+1369d others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
CTG | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0021others(32): Show | 35 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.908+1368_908+1369d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
CTGTG | C | 70 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.908+1366_908+1369d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702135
|
CTGTGTG | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0043others(1): Show | 4 | HG01346.hp2 HG01358.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+1364_908+1369d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | ||||||
chr22:28702172
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0321 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.908+1332_908+1333i others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702172 | ||||||
chr22:28702233
|
A | AT | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.908+1271dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702233 | ||||||
chr22:28702233
|
AT | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0032others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1271delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702233 | ||||||
chr22:28702261
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.908+1244G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702261 | ||||||
chr22:28702290
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0084a0001c0001t0001g0165others(3): Show | 6 | HG00438.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1215T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702290 | ||||||
chr22:28702299
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.908+1206G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702299 | ||||||
chr22:28702301
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0360 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.908+1204G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702301 | ||||||
chr22:28702324
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.908+1181G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702324 | ||||||
chr22:28702331
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0071 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.908+1174A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702331 | ||||||
chr22:28702383
|
A | C | 7 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0366others(4): Show | 7 | HG00673.hp1 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1122T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702383 | ||||||
chr22:28702383
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+1122T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702383 | ||||||
chr22:28702384
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+1121C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702384 | ||||||
chr22:28702387
|
C | T | 1 | a0008c0005t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.908+1118G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702387 | ||||||
chr22:28702388
|
A | G | 1 | a0008c0005t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.908+1117T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702388 | ||||||
chr22:28702396
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1109T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702396 | ||||||
chr22:28702400
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1105T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702400 | ||||||
chr22:28702429
|
A | G | 31 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0001g0146others(28): Show | 31 | HG00673.hp1 HG01123.hp2 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.908+1076T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702429 | ||||||
chr22:28702436
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1069G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702436 | ||||||
chr22:28702444
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.908+1061A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702444 | ||||||
chr22:28702450
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.908+1055C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702450 | ||||||
chr22:28702454
|
G | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1051C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702454 | ||||||
chr22:28702455
|
G | A | 2 | a0001c0001t0001g0011a0001c0002t0001g0344 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.908+1050C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702455 | ||||||
chr22:28702456
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0143a0001c0001t0001g0161others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.908+1049G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702456 | ||||||
chr22:28702473
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0138a0001c0001t0001g0194 | 3 | HG01346.hp2 HG01358.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.908+1032A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702473 | ||||||
chr22:28702537
|
CT | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.908+967delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702537 | ||||||
chr22:28702588
|
C | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.908+917G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702588 | ||||||
chr22:28702827
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+678C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702827 | ||||||
chr22:28702857
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.908+648A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702857 | ||||||
chr22:28702942
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0196others(1): Show | 4 | HG03654.hp2 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+563A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702942 | ||||||
chr22:28703363
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.908+142A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703363 | ||||||
chr22:28703371
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0264 | 2 | NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.908+134G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703371 | ||||||
chr22:28703400
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.908+105C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703400 | ||||||
chr22:28703411
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.908+94G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703411 | ||||||
chr22:28703766
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.847-200A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28703766 | ||||||
chr22:28703962
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.847-396G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28703962 | ||||||
chr22:28704121
|
G | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0355 | 2 | HG00673.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.847-555C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
G | GAC | 12 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0078others(9): Show | 12 | HG00099.hp1 HG01975.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-557_847-556dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
G | GACAC | 4 | a0001c0001t0001g0025a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-559_847-556dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GAC | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 131 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.847-557_847-556del others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GACAC | G | 28 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 28 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-559_847-556del others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GACACAC | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.847-561_847-556del others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GACACACA others(1): Show |
G | 52 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0017others(49): Show | 53 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.847-563_847-556del others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GACACACA others(3): Show |
G | 1 | a0001c0001t0001g0222 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.847-565_847-556del others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704121
|
GACACACA others(7): Show |
G | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0188 | 3 | HG02015.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.847-569_847-556del others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | ||||||
chr22:28704125
|
C | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.847-559G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704125 | ||||||
chr22:28704127
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.847-561G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704127 | ||||||
chr22:28704192
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.847-626G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704192 | ||||||
chr22:28704205
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.847-639T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704205 | ||||||
chr22:28704302
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847-736A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704302 | ||||||
chr22:28704313
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0079 | 2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.847-747A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704313 | ||||||
chr22:28704316
|
T | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.847-750A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704316 | ||||||
chr22:28704372
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.847-806C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704372 | ||||||
chr22:28704458
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-892C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704458 | ||||||
chr22:28704576
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.847-1010T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704576 | ||||||
chr22:28704608
|
C | T | 1 | a0003c0007t0001g0297 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.847-1042G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704608 | ||||||
chr22:28704639
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.847-1073G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704639 | ||||||
chr22:28704678
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.847-1112C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704678 | ||||||
chr22:28704723
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.847-1157A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704723 | ||||||
chr22:28704727
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0097 | 2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.847-1161G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704727 | ||||||
chr22:28704895
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.847-1329T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704895 | ||||||
chr22:28704901
|
C | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-1335G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704901 | ||||||
chr22:28704989
|
C | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.847-1423G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704989 | ||||||
chr22:28704997
|
G | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.847-1431C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704997 | ||||||
chr22:28705078
|
CT | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0048others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.847-1513delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705078 | ||||||
chr22:28705127
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.847-1561C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705127 | ||||||
chr22:28705319
|
C | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0031others(11): Show | 14 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.847-1753G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705319 | ||||||
chr22:28705369
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.847-1803T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705369 | ||||||
chr22:28705549
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.847-1983T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705549 | ||||||
chr22:28705612
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0085others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.847-2046T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705612 | ||||||
chr22:28705648
|
G | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-2082C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705648 | ||||||
chr22:28705790
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-2224C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705790 | ||||||
chr22:28705803
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.847-2237C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705803 | ||||||
chr22:28705841
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0085others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.847-2275C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705841 | ||||||
chr22:28705852
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.847-2286C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705852 | ||||||
chr22:28705968
|
A | AAAACT | 29 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(26): Show | 29 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.847-2407_847-2403d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | ||||||
chr22:28705968
|
A | AAAACTAA others(3): Show |
163 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.847-2412_847-2403d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | ||||||
chr22:28705968
|
A | AAAACTAA others(8): Show |
162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 163 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.847-2417_847-2403d others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | ||||||
chr22:28705968
|
A | AAAACTAA others(13): Show |
15 | a0001c0001t0001g0015a0001c0001t0001g0155a0001c0001t0001g0198others(12): Show | 15 | HG00597.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.847-2422_847-2403d others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | ||||||
chr22:28705991
|
A | ACTAAACT others(8): Show |
1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.847-2426_847-2425i others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705991 | ||||||
chr22:28706064
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.847-2498G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706064 | ||||||
chr22:28706129
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.847-2563A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706129 | ||||||
chr22:28706296
|
G | GCT | 8 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0058others(5): Show | 8 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-2732_847-2731d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706296 | ||||||
chr22:28706298
|
T | TCA | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(44): Show | 47 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.847-2734_847-2733d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | ||||||
chr22:28706298
|
T | TCACA | 3 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0337 | 3 | HG02155.hp1 NA18980.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.847-2736_847-2733d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | ||||||
chr22:28706298
|
TCA | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.847-2734_847-2733d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | ||||||
chr22:28706298
|
TCACA | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0282a0001c0001t0001g0317 | 3 | HG02273.hp2 HG03831.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.847-2736_847-2733d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | ||||||
chr22:28706298
|
TCACACA | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0085others(111): Show | 114 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.847-2738_847-2733d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | ||||||
chr22:28706300
|
A | T | 20 | a0001c0001t0001g0042a0001c0001t0001g0081a0001c0001t0001g0082others(17): Show | 20 | HG00544.hp1 HG02486.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.847-2734T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706300 | ||||||
chr22:28706332
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.847-2766T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706332 | ||||||
chr22:28706347
|
A | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0085a0001c0001t0001g0123others(43): Show | 46 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.847-2781T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706347 | ||||||
chr22:28706505
|
GTGATCAT others(14): Show |
G | 1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.847-2960_847-2940d others(23): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706505 | ||||||
chr22:28706550
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0034a0006c0006t0001g0137 | 3 | HG02647.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.847-2984G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706550 | ||||||
chr22:28706578
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.847-3012C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706578 | ||||||
chr22:28706657
|
G | A | 26 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(23): Show | 26 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.847-3091C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706657 | ||||||
chr22:28706713
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0093 | 3 | HG03927.hp2 NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.847-3147C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706713 | ||||||
chr22:28706717
|
G | T | 1 | a0001c0001t0001g0331 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.847-3151C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706717 | ||||||
chr22:28706780
|
C | T | 2 | a0001c0001t0001g0373a0001c0001t0001g0374 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.847-3214G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706780 | ||||||
chr22:28706792
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0238 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.846+3214C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706792 | ||||||
chr22:28706855
|
GC | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0331a0001c0001t0001g0335others(6): Show | 10 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+3150delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706855 | ||||||
chr22:28706857
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0331a0001c0001t0001g0335others(6): Show | 10 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+3149T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706857 | ||||||
chr22:28706978
|
G | A | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+3028C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706978 | ||||||
chr22:28706979
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.846+3027C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706979 | ||||||
chr22:28707060
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.846+2946A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707060 | ||||||
chr22:28707093
|
TAGTC | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.846+2909_846+2912d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707093 | ||||||
chr22:28707229
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0085others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.846+2777C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707229 | ||||||
chr22:28707252
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.846+2754G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707252 | ||||||
chr22:28707253
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2753C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707253 | ||||||
chr22:28707305
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2701C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707305 | ||||||
chr22:28707353
|
T | C | 14 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0155others(11): Show | 14 | HG01891.hp1 HG02056.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.846+2653A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707353 | ||||||
chr22:28707465
|
C | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2541G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707465 | ||||||
chr22:28707504
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0222 | 2 | HG00280.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.846+2502A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707504 | ||||||
chr22:28707618
|
A | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2388T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707618 | ||||||
chr22:28707781
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.846+2225A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707781 | ||||||
chr22:28707830
|
C | CT | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.846+2175dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | ||||||
chr22:28707830
|
C | CTT | 41 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0001t0001g0104others(38): Show | 41 | HG00323.hp1 HG00642.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.846+2174_846+2175d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | ||||||
chr22:28707830
|
CT | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0047others(5): Show | 8 | HG02559.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+2175delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | ||||||
chr22:28707923
|
G | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2083C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707923 | ||||||
chr22:28707979
|
C | T | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+2027G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707979 | ||||||
chr22:28708003
|
A | AT | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2002dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708003 | ||||||
chr22:28708041
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0344a0001c0002t0002g0379others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+1965C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708041 | ||||||
chr22:28708118
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.846+1888G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708118 | ||||||
chr22:28708201
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0136 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.846+1805A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708201 | ||||||
chr22:28708361
|
A | ATGTG | 9 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 10 | HG00140.hp1 HG01175.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTG | 4 | a0001c0001t0001g0110a0001c0001t0001g0180a0001c0001t0001g0190others(1): Show | 4 | HG00099.hp2 HG04228.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTGT others(1): Show |
25 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0104others(22): Show | 25 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTGT others(3): Show |
19 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0117others(16): Show | 19 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTGT others(5): Show |
8 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0175others(5): Show | 8 | HG00735.hp2 HG02071.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0126 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.846+1644_846+1645i others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708361
|
A | ATGTGTGT others(9): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0181 | 2 | HG01106.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.846+1644_846+1645i others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | ||||||
chr22:28708363
|
A | ATG | 21 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(18): Show | 22 | HG01123.hp1 HG01175.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.846+1641_846+1642d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTG | 17 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0032others(14): Show | 17 | HG00423.hp2 HG00642.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.846+1639_846+1642d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTG | 17 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 17 | HG00280.hp1 HG01099.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.846+1637_846+1642d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(1): Show |
26 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0030others(23): Show | 26 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.846+1635_846+1642d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(3): Show |
21 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.846+1633_846+1642d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(5): Show |
9 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0053others(6): Show | 9 | HG01981.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+1631_846+1642d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(7): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0070others(6): Show | 9 | HG00735.hp1 HG01069.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+1629_846+1642d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0080 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.846+1627_846+1642d others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0001g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.846+1625_846+1642d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0077others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.846+1643T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708363
|
ATG | A | 31 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.846+1641_846+1642d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | ||||||
chr22:28708367
|
G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0225 | 3 | HG00280.hp2 HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.846+1638_846+1639i others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708367 | ||||||
chr22:28708369
|
G | GTGTGTGT others(3): Show |
37 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(34): Show | 37 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.846+1636_846+1637i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708369 | ||||||
chr22:28708373
|
G | GTGTGTC | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+1632_846+1633i others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708373 | ||||||
chr22:28708692
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.846+1314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708692 | ||||||
chr22:28708742
|
T | G | 1 | a0001c0001t0001g0349 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.846+1264A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708742 | ||||||
chr22:28708782
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.846+1224A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708782 | ||||||
chr22:28708866
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.846+1140A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708866 | ||||||
chr22:28708952
|
C | CA | 15 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0023others(12): Show | 15 | HG00423.hp2 HG00544.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.846+1053dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | ||||||
chr22:28708952
|
CA | C | 19 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(16): Show | 19 | HG00597.hp2 HG00673.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.846+1053delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | ||||||
chr22:28708952
|
CAA | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.846+1052_846+1053d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | ||||||
chr22:28708963
|
A | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0334 | 2 | HG02602.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.846+1043T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708963 | ||||||
chr22:28708967
|
A | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.846+1039T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708967 | ||||||
chr22:28708971
|
A | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.846+1035T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708971 | ||||||
chr22:28708979
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+1027G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708979 | ||||||
chr22:28708990
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0031 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.846+1016G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708990 | ||||||
chr22:28709029
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.846+977A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709029 | ||||||
chr22:28709036
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.846+970C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709036 | ||||||
chr22:28709044
|
T | C | 1 | a0001c0001t0001g0358 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.846+962A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709044 | ||||||
chr22:28709214
|
G | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0221a0001c0001t0001g0225others(4): Show | 7 | HG00323.hp1 HG01071.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.846+792C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709214 | ||||||
chr22:28709231
|
A | G | 2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.846+775T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709231 | ||||||
chr22:28709279
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.846+727C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709279 | ||||||
chr22:28709427
|
G | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.846+579C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709427 | ||||||
chr22:28709459
|
C | A | 4 | a0001c0001t0001g0271a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | HG02027.hp1 HG02165.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+547G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709459 | ||||||
chr22:28709539
|
A | C | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+467T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709539 | ||||||
chr22:28709570
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 163 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.846+436T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709570 | ||||||
chr22:28709622
|
C | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.846+384G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709622 | ||||||
chr22:28709726
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.846+280G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709726 | ||||||
chr22:28709864
|
C | A | 1 | a0001c0001t0001g0253 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.846+142G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709864 | ||||||
chr22:28709868
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.846+138C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709868 | ||||||
chr22:28710186
|
A | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.793-127T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710186 | ||||||
chr22:28710361
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0034a0006c0006t0001g0137 | 3 | HG02647.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.793-302T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710361 | ||||||
chr22:28710559
|
G | C | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-500C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710559 | ||||||
chr22:28710745
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(122): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.793-686A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710745 | ||||||
chr22:28710957
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(122): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.793-898C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710957 | ||||||
chr22:28710979
|
T | C | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-920A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710979 | ||||||
chr22:28711207
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.792+702C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711207 | ||||||
chr22:28711405
|
C | CA | 4 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG01099.hp2 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+503dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711405 | ||||||
chr22:28711584
|
G | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+325C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711584 | ||||||
chr22:28711726
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.792+183T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711726 | ||||||
chr22:28711781
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG01257.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.792+128C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711781 | ||||||
chr22:28712085
|
C | A | 1 | a0001c0001t0001g0357 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.684-68G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712085 | ||||||
chr22:28712091
|
C | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0298 | 2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.684-74G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712091 | ||||||
chr22:28712094
|
G | GTATTAGA others(16): Show |
28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.684-100_684-78dupT others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712094 | ||||||
chr22:28712124
|
A | C | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.684-107T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712124 | ||||||
chr22:28712139
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.684-122G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712139 | ||||||
chr22:28712241
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.684-224T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712241 | ||||||
chr22:28712388
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG01243.hp1 HG02723.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-371T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712388 | ||||||
chr22:28712456
|
T | C | 34 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(31): Show | 34 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.684-439A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712456 | ||||||
chr22:28712568
|
A | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.684-551T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712568 | ||||||
chr22:28712707
|
G | A | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-690C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712707 | ||||||
chr22:28712814
|
T | A | 1 | a0001c0001t0001g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684-797A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712814 | ||||||
chr22:28713020
|
T | G | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-1003A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713020 | ||||||
chr22:28713048
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.684-1031G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713048 | ||||||
chr22:28713131
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-1114T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713131 | ||||||
chr22:28713176
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0217 | 2 | NA18944.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.684-1159T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713176 | ||||||
chr22:28713194
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.684-1177T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713194 | ||||||
chr22:28713209
|
C | T | 12 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.684-1192G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713209 | ||||||
chr22:28713362
|
C | CT | 27 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(24): Show | 27 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.684-1346dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713362 | ||||||
chr22:28713365
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-1348A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713365 | ||||||
chr22:28713398
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0139 | 2 | HG00544.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.684-1381G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713398 | ||||||
chr22:28713421
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.684-1404C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713421 | ||||||
chr22:28713445
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.684-1428G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713445 | ||||||
chr22:28713636
|
G | A | 22 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.684-1619C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713636 | ||||||
chr22:28713697
|
T | G | 3 | a0001c0001t0001g0329a0001c0001t0001g0333a0001c0001t0001g0372 | 3 | HG02257.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.684-1680A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713697 | ||||||
chr22:28713853
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.684-1836C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713853 | ||||||
chr22:28713923
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.684-1906A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713923 | ||||||
chr22:28714014
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(122): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.684-1997A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714014 | ||||||
chr22:28714175
|
C | T | 1 | a0002c0011t0001g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.684-2158G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714175 | ||||||
chr22:28714499
|
T | C | 2 | a0001c0001t0001g0373a0001c0001t0001g0374 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.684-2482A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714499 | ||||||
chr22:28714516
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.684-2499C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714516 | ||||||
chr22:28714771
|
C | G | 84 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.684-2754G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714771 | ||||||
chr22:28715138
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.684-3121A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715138 | ||||||
chr22:28715380
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.684-3363A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715380 | ||||||
chr22:28715397
|
T | TTTTA | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.684-3384_684-3381d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715397 | ||||||
chr22:28715530
|
T | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.684-3513A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715530 | ||||||
chr22:28715626
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG02145.hp1 HG02630.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3609C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715626 | ||||||
chr22:28715688
|
C | T | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3671G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715688 | ||||||
chr22:28716170
|
G | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683+3225C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716170 | ||||||
chr22:28716199
|
C | CT | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0042others(26): Show | 29 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.683+3195dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716199 | ||||||
chr22:28716199
|
CT | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.683+3195delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716199 | ||||||
chr22:28716222
|
A | T | 1 | a0003c0007t0001g0297 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.683+3173T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716222 | ||||||
chr22:28716250
|
G | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.683+3145C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716250 | ||||||
chr22:28716371
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG00423.hp2 HG03927.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+3024T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716371 | ||||||
chr22:28716484
|
A | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.683+2911T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716484 | ||||||
chr22:28716491
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.683+2904G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716491 | ||||||
chr22:28716612
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683+2783G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716612 | ||||||
chr22:28716660
|
C | T | 4 | a0001c0002t0001g0006a0001c0002t0001g0344a0001c0002t0002g0379others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+2735G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716660 | ||||||
chr22:28716940
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.683+2455C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716940 | ||||||
chr22:28717062
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.683+2333A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717062 | ||||||
chr22:28717155
|
GATC | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.683+2237_683+2239d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717155 | ||||||
chr22:28717235
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.683+2160C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717235 | ||||||
chr22:28717336
|
C | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 6 | HG00597.hp2 HG00621.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.683+2059G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717336 | ||||||
chr22:28717354
|
G | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683+2041C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717354 | ||||||
chr22:28717531
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.683+1864G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717531 | ||||||
chr22:28717885
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.683+1510C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717885 | ||||||
chr22:28717937
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.683+1458G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717937 | ||||||
chr22:28718013
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.683+1382C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718013 | ||||||
chr22:28718023
|
G | C | 2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.683+1372C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718023 | ||||||
chr22:28718037
|
C | T | 1 | a0001c0001t0001g0327 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.683+1358G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718037 | ||||||
chr22:28718118
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.683+1277G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718118 | ||||||
chr22:28718401
|
T | A | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+994A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718401 | ||||||
chr22:28718582
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.683+813T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718582 | ||||||
chr22:28718812
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.683+583C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718812 | ||||||
chr22:28718837
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.683+558C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718837 | ||||||
chr22:28718883
|
A | AAC | 60 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(57): Show | 60 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.683+510_683+511dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
A | AACAC | 41 | a0001c0001t0001g0002a0001c0001t0001g0102a0001c0001t0001g0106others(38): Show | 42 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.683+508_683+511dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
A | AACACAC | 16 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0109others(13): Show | 16 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.683+506_683+511dup others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
A | AACACACA others(1): Show |
13 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.683+504_683+511dup others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0088 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.683+502_683+511dup others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0351 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.683+500_683+511dup others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
AAC | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 76 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.683+510_683+511del others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
AACAC | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.683+508_683+511del others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
AACACAC | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.683+506_683+511del others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0002t0001g0363 | 3 | HG04228.hp2 NA18994.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.683+504_683+511del others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28718883
|
AACACACA others(3): Show |
A | 7 | a0001c0002t0001g0364a0001c0002t0001g0365a0001c0002t0001g0366others(4): Show | 7 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.683+502_683+511del others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | ||||||
chr22:28719003
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.683+392C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719003 | ||||||
chr22:28719047
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.683+348G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719047 | ||||||
chr22:28719078
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.683+317G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719078 | ||||||
chr22:28719499
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0286 | 3 | HG02698.hp1 NA18982.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.593-14C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719499 | ||||||
chr22:28719660
|
T | C | 1 | a0001c0002t0001g0365 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.593-175A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719660 | ||||||
chr22:28719772
|
C | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.593-287G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719772 | ||||||
chr22:28719844
|
A | C | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-359T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719844 | ||||||
chr22:28719975
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.593-490A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719975 | ||||||
chr22:28720092
|
A | AT | 92 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-608dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | ||||||
chr22:28720092
|
A | ATT | 59 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0065others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.593-609_593-608dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | ||||||
chr22:28720092
|
AT | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.593-608delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | ||||||
chr22:28720212
|
T | C | 1 | a0001c0001t0001g0351 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.593-727A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720212 | ||||||
chr22:28720251
|
C | T | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-766G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720251 | ||||||
chr22:28720411
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.593-926T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720411 | ||||||
chr22:28720635
|
G | A | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-1150C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720635 | ||||||
chr22:28720806
|
T | C | 1 | a0001c0002t0001g0344 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.593-1321A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720806 | ||||||
chr22:28721178
|
T | C | 1 | a0001c0001t0001g0354 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.593-1693A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721178 | ||||||
chr22:28721228
|
A | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1743T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721228 | ||||||
chr22:28721281
|
G | GT | 106 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0024others(103): Show | 106 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.593-1797dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | ||||||
chr22:28721281
|
G | GTT | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(75): Show | 79 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.593-1798_593-1797d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | ||||||
chr22:28721281
|
G | GTTT | 28 | a0001c0001t0001g0004a0001c0001t0001g0120a0001c0001t0001g0121others(25): Show | 28 | HG01243.hp2 HG01358.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-1799_593-1797d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | ||||||
chr22:28721281
|
G | T | 1 | a0001c0002t0001g0364 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.593-1796C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | ||||||
chr22:28721282
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.593-1797A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721282 | ||||||
chr22:28721320
|
C | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0055others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1835G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721320 | ||||||
chr22:28721922
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-2437C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721922 | ||||||
chr22:28722259
|
CGCCGGGC others(1051): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.592+1660_592+2717d others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722259 | ||||||
chr22:28722332
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.592+2645T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722332 | ||||||
chr22:28722339
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.592+2638C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722339 | ||||||
chr22:28722397
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+2580C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722397 | ||||||
chr22:28722401
|
G | A | 2 | a0001c0001t0001g0373a0001c0001t0001g0374 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.592+2576C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722401 | ||||||
chr22:28722428
|
T | G | 1 | a0001c0001t0001g0319 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.592+2549A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722428 | ||||||
chr22:28722533
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.592+2444G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722533 | ||||||
chr22:28722539
|
C | CA | 13 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 13 | HG00673.hp1 HG01175.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+2437dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | ||||||
chr22:28722539
|
C | CAA | 8 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0191others(5): Show | 8 | HG02559.hp1 HG03516.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+2436_592+2437d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | ||||||
chr22:28722539
|
CA | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0017others(153): Show | 157 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.592+2437delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | ||||||
chr22:28722554
|
AAAAAAGA others(4): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592+2412_592+2422d others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722554 | ||||||
chr22:28722556
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0272 | 2 | HG01261.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.592+2421T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722556 | ||||||
chr22:28722559
|
AG | A | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(11): Show | 14 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+2417delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722559 | ||||||
chr22:28722560
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+2417C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722560 | ||||||
chr22:28722575
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.592+2402C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722575 | ||||||
chr22:28722728
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+2249A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722728 | ||||||
chr22:28722768
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592+2209T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722768 | ||||||
chr22:28722974
|
C | T | 9 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(6): Show | 9 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.592+2003G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722974 | ||||||
chr22:28723024
|
C | G | 1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.592+1953G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723024 | ||||||
chr22:28723215
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1762A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723215 | ||||||
chr22:28723232
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(122): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.592+1745C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723232 | ||||||
chr22:28723337
|
G | A | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02027.hp1 HG02165.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+1640C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723337 | ||||||
chr22:28723391
|
G | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0289 | 2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.592+1586C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723391 | ||||||
chr22:28723408
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+1569G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723408 | ||||||
chr22:28723411
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.592+1566T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723411 | ||||||
chr22:28723523
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.592+1454C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723523 | ||||||
chr22:28723599
|
A | AG | 3 | a0001c0001t0001g0086a0001c0001t0001g0158a0001c0001t0001g0210 | 3 | NA18948.hp1 NA18992.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.592+1377dupC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723599 | ||||||
chr22:28723601
|
G | GA | 155 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 156 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.592+1375dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723601 | ||||||
chr22:28723601
|
G | GAA | 21 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0159others(18): Show | 21 | HG00621.hp1 HG01243.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1374_592+1375d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723601 | ||||||
chr22:28723602
|
A | G | 15 | a0001c0001t0001g0147a0001c0001t0001g0209a0001c0001t0001g0211others(12): Show | 15 | NA18939.hp1 NA18944.hp1 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+1375T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723602 | ||||||
chr22:28723609
|
AAG | A | 7 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(4): Show | 7 | HG00438.hp2 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.592+1366_592+1367d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723609 | ||||||
chr22:28723610
|
AG | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0057others(3): Show | 6 | HG00673.hp1 HG01081.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+1366delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723610 | ||||||
chr22:28723611
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.592+1366C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723611 | ||||||
chr22:28723663
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.592+1314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723663 | ||||||
chr22:28723684
|
C | A | 1 | a0001c0001t0001g0284 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592+1293G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723684 | ||||||
chr22:28723810
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.592+1167C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723810 | ||||||
chr22:28723813
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1164C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723813 | ||||||
chr22:28723930
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1047A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723930 | ||||||
chr22:28723998
|
G | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+979C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723998 | ||||||
chr22:28724145
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0197 | 2 | NA18946.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.592+832G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724145 | ||||||
chr22:28724146
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+831C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724146 | ||||||
chr22:28724159
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.592+818C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724159 | ||||||
chr22:28724235
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+742C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724235 | ||||||
chr22:28724412
|
A | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.592+565T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724412 | ||||||
chr22:28724418
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.592+559T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724418 | ||||||
chr22:28724501
|
G | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+476C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724501 | ||||||
chr22:28724616
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+361C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724616 | ||||||
chr22:28724698
|
C | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+279G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724698 | ||||||
chr22:28724809
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.592+168T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724809 | ||||||
chr22:28724878
|
T | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.592+99A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724878 | ||||||
chr22:28724888
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.592+89T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724888 | ||||||
chr22:28725488
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.320-121C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725488 | ||||||
chr22:28725680
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0136 | 3 | HG01496.hp2 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.320-313C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725680 | ||||||
chr22:28725768
|
G | T | 6 | a0001c0002t0001g0006a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-401C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725768 | ||||||
chr22:28725772
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(122): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.320-405C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725772 | ||||||
chr22:28725864
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG00741.hp1 HG03831.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.320-497C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725864 | ||||||
chr22:28725908
|
C | CA | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.320-542dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725908 | ||||||
chr22:28725908
|
C | CAA | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0085others(11): Show | 14 | HG00642.hp1 HG01358.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.320-543_320-542dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725908 | ||||||
chr22:28725922
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-555A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725922 | ||||||
chr22:28726159
|
C | T | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-792G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726159 | ||||||
chr22:28726173
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.320-806T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726173 | ||||||
chr22:28726210
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.320-843T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726210 | ||||||
chr22:28726380
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320-1013A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726380 | ||||||
chr22:28726469
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.320-1102T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726469 | ||||||
chr22:28726495
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.320-1128A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726495 | ||||||
chr22:28726763
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.320-1396G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726763 | ||||||
chr22:28726847
|
C | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-1480G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726847 | ||||||
chr22:28727215
|
G | A | 2 | a0001c0001t0001g0376a0001c0001t0001g0377 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.320-1848C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727215 | ||||||
chr22:28727250
|
A | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.320-1883T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727250 | ||||||
chr22:28727402
|
A | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-2035T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727402 | ||||||
chr22:28727593
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0138 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.320-2226A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727593 | ||||||
chr22:28727664
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-2297G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727664 | ||||||
chr22:28727687
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-2320A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727687 | ||||||
chr22:28727807
|
T | G | 17 | a0001c0001t0001g0147a0001c0001t0001g0158a0001c0001t0001g0209others(14): Show | 17 | NA18939.hp1 NA18944.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.320-2440A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727807 | ||||||
chr22:28727858
|
T | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.320-2491A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727858 | ||||||
chr22:28727883
|
C | CG | 18 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0033others(15): Show | 18 | HG00673.hp1 HG00735.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.320-2517dupC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727883 | ||||||
chr22:28728002
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-2635G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728002 | ||||||
chr22:28728005
|
A | G | 368 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(365): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.320-2638T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728005 | ||||||
chr22:28728005
|
A | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.320-2638T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728005 | ||||||
chr22:28728196
|
C | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.320-2829G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728196 | ||||||
chr22:28728290
|
TAAAAAGA others(11): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.320-2941_320-2924d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728290 | ||||||
chr22:28728302
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.320-2935A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728302 | ||||||
chr22:28728422
|
G | A | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-3055C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728422 | ||||||
chr22:28728787
|
T | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG00558.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.320-3420A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728787 | ||||||
chr22:28728829
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.320-3462T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728829 | ||||||
chr22:28728898
|
A | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-3531T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728898 | ||||||
chr22:28728956
|
A | AAC | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-3590_320-3589i others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728956 | ||||||
chr22:28728972
|
C | CT | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3606dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728972 | ||||||
chr22:28728974
|
C | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3607G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728974 | ||||||
chr22:28728974
|
C | CA | 358 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(355): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.320-3608dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728974 | ||||||
chr22:28729088
|
G | A | 50 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0152others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-3721C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729088 | ||||||
chr22:28729425
|
C | T | 4 | a0001c0002t0001g0006a0001c0002t0001g0344a0001c0002t0002g0379others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-4058G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729425 | ||||||
chr22:28729434
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.320-4067G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729434 | ||||||
chr22:28729494
|
G | GATCACGC others(4): Show |
1 | a0001c0001t0001g0149 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.320-4138_320-4128d others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729494 | ||||||
chr22:28729522
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0346a0001c0001t0001g0362 | 3 | HG02559.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.320-4155C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729522 | ||||||
chr22:28729540
|
C | CA | 12 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01099.hp2 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-4174dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(5): Show |
2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.320-4185_320-4174d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(6): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0344 | 2 | HG02257.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.320-4186_320-4174d others(15): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0019 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.320-4187_320-4174d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320-4188_320-4174d others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(10): Show |
3 | a0001c0002t0001g0364a0001c0002t0001g0365a0001c0002t0001g0366 | 3 | HG00438.hp2 HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.320-4190_320-4174d others(19): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(11): Show |
3 | a0001c0002t0001g0367a0001c0002t0001g0368a0001c0002t0001g0369 | 3 | HG02015.hp2 HG02129.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.320-4191_320-4174d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0363 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.320-4196_320-4174d others(25): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
C | CAAAAAAA others(25): Show |
1 | a0001c0002t0001g0370 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.320-4174_320-4173i others(34): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
CAAAA | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0116others(20): Show | 24 | HG00738.hp1 HG01433.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.320-4177_320-4174d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
CAAAAA | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.320-4178_320-4174d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
CAAAAAA | C | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0171others(4): Show | 7 | HG01943.hp1 HG02698.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-4179_320-4174d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729540
|
CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-4181_320-4174d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | ||||||
chr22:28729566
|
G | T | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-4199C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729566 | ||||||
chr22:28729579
|
A | C | 18 | a0001c0001t0001g0147a0001c0001t0001g0158a0001c0001t0001g0209others(15): Show | 18 | HG02683.hp2 NA18939.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-4212T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729579 | ||||||
chr22:28729742
|
T | G | 374 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(371): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.320-4375A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729742 | ||||||
chr22:28729848
|
T | C | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.320-4481A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729848 | ||||||
chr22:28729927
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.319+4476A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729927 | ||||||
chr22:28729984
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319+4419G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729984 | ||||||
chr22:28730001
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.319+4402C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730001 | ||||||
chr22:28730197
|
A | G | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.319+4206T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730197 | ||||||
chr22:28730209
|
A | C | 1 | a0001c0001t0001g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4194T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730209 | ||||||
chr22:28730226
|
G | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.319+4177C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730226 | ||||||
chr22:28730236
|
GAA | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4165_319+4166d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730236 | ||||||
chr22:28730240
|
A | AGAGGAGG others(6): Show |
1 | a0001c0001t0001g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+4162_319+4163i others(15): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730240 | ||||||
chr22:28730241
|
G | T | 3 | a0001c0002t0001g0006a0001c0002t0002g0379a0001c0002t0002g0380 | 3 | HG01891.hp2 HG03516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.319+4162C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730241 | ||||||
chr22:28730252
|
A | G | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4151T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730252 | ||||||
chr22:28730263
|
G | GAGGAGAG others(180): Show |
1 | a0001c0001t0001g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4139_319+4140i others(189): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730263 | ||||||
chr22:28730264
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4139C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(173): Show |
4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG00741.hp2 HG01168.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(188): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(197): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(178): Show |
1 | a0001c0003t0001g0051 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(178): Show |
67 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(183): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(20): Show | 25 | HG01192.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(192): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(179): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(184): Show |
1 | a0001c0001t0001g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(193): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0065 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(173): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(159): Show |
1 | a0001c0001t0001g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(168): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(178): Show |
1 | a0001c0001t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(183): Show |
1 | a0001c0001t0001g0246 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(192): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(155): Show |
13 | a0001c0001t0001g0042a0001c0001t0001g0102a0001c0001t0001g0231others(10): Show | 13 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(164): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(173): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0138 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(149): Show |
1 | a0001c0001t0001g0283 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(158): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(132): Show |
1 | a0001c0001t0001g0229 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(141): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(160): Show |
5 | a0001c0002t0001g0006a0001c0002t0001g0020a0001c0002t0001g0344others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(169): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(165): Show |
1 | a0001c0001t0001g0148 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(174): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(131): Show |
15 | a0001c0001t0001g0010a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(140): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(136): Show |
43 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0146others(40): Show | 44 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(145): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(151): Show |
1 | a0001c0001t0001g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(160): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(137): Show |
38 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(142): Show |
2 | a0001c0001t0001g0343a0001c0001t0001g0359 | 2 | HG03710.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(151): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(144): Show |
1 | a0001c0001t0001g0257 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(153): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(147): Show |
109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0123others(106): Show | 110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(156): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(152): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0281 | 2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(161): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(162): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(171): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(138): Show |
1 | a0001c0001t0001g0264 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(147): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(148): Show |
6 | a0001c0001t0001g0048a0001c0001t0001g0157a0001c0001t0001g0282others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(157): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0201 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0349 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(152): Show |
1 | a0001c0001t0001g0284 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(161): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0197 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(136): Show |
1 | a0001c0001t0001g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(145): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(148): Show |
1 | a0001c0001t0001g0285 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(157): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGAGAG others(149): Show |
1 | a0001c0001t0001g0204 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(158): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGGGAG others(206): Show |
3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(215): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGGGAG others(165): Show |
1 | a0001c0002t0001g0019 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(174): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGGGAG others(141): Show |
1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(150): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGGGAG others(132): Show |
8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(141): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730264
|
G | GAGGGGAG others(168): Show |
1 | a0001c0001t0001g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(177): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | ||||||
chr22:28730269
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4134T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730269 | ||||||
chr22:28730271
|
G | GGAGAGGA others(125): Show |
1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4131_319+4132i others(134): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730271 | ||||||
chr22:28730274
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4129T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730274 | ||||||
chr22:28730277
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4126G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730277 | ||||||
chr22:28730316
|
CAGAAG | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4082_319+4086d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730316 | ||||||
chr22:28730326
|
A | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4077T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730326 | ||||||
chr22:28730359
|
GAAAGGA | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.319+4038_319+4043d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730359 | ||||||
chr22:28730629
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0161a0001c0002t0001g0006 | 3 | HG02109.hp1 HG04184.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.319+3774C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730629 | ||||||
chr22:28730726
|
C | CATA | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3674_319+3676d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730726 | ||||||
chr22:28730782
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0042others(14): Show | 17 | HG01346.hp2 HG01358.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+3621G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730782 | ||||||
chr22:28731073
|
C | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3330G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731073 | ||||||
chr22:28731159
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.319+3244A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731159 | ||||||
chr22:28731207
|
TAAAC | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3192_319+3195d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731207 | ||||||
chr22:28731236
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0163others(35): Show | 39 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+3167T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731236 | ||||||
chr22:28731317
|
G | A | 1 | a0001c0002t0002g0379 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.319+3086C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731317 | ||||||
chr22:28731325
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.319+3078C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731325 | ||||||
chr22:28731369
|
C | T | 1 | a0001c0002t0001g0363 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.319+3034G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731369 | ||||||
chr22:28731414
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.319+2989A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731414 | ||||||
chr22:28731424
|
A | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.319+2979T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731424 | ||||||
chr22:28731427
|
C | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2976G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731427 | ||||||
chr22:28731442
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319+2961T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731442 | ||||||
chr22:28731559
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.319+2844C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731559 | ||||||
chr22:28731630
|
CTATT | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2769_319+2772d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731630 | ||||||
chr22:28731964
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.319+2439G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731964 | ||||||
chr22:28732025
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.319+2378A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732025 | ||||||
chr22:28732099
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.319+2304C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732099 | ||||||
chr22:28732135
|
G | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2268C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732135 | ||||||
chr22:28732402
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319+2001G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732402 | ||||||
chr22:28732509
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+1894G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732509 | ||||||
chr22:28732526
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.319+1877G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732526 | ||||||
chr22:28732545
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319+1858A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732545 | ||||||
chr22:28732630
|
A | ATTG | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+1772_319+1773i others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732630 | ||||||
chr22:28732807
|
G | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+1596C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732807 | ||||||
chr22:28732814
|
G | GA | 8 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0023others(5): Show | 8 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1588dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732814 | ||||||
chr22:28732829
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.319+1574A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732829 | ||||||
chr22:28732839
|
C | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+1564G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732839 | ||||||
chr22:28732883
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.319+1520G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732883 | ||||||
chr22:28732901
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.319+1502G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732901 | ||||||
chr22:28733252
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319+1151C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733252 | ||||||
chr22:28733372
|
T | C | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1031A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733372 | ||||||
chr22:28733652
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319+751G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733652 | ||||||
chr22:28733737
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.319+666C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733737 | ||||||
chr22:28733753
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.319+650A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733753 | ||||||
chr22:28733900
|
C | A | 1 | a0001c0001t0001g0323 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.319+503G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733900 | ||||||
chr22:28733922
|
C | CA | 23 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(20): Show | 23 | HG00423.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+480dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733922 | ||||||
chr22:28733922
|
CA | C | 19 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(16): Show | 19 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.319+480delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733922 | ||||||
chr22:28734011
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+392A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734011 | ||||||
chr22:28734024
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.319+379A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734024 | ||||||
chr22:28734093
|
A | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+310T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734093 | ||||||
chr22:28734224
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+179A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734224 | ||||||
chr22:28734312
|
C | T | 103 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.319+91G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734312 | ||||||
chr22:28734359
|
G | GT | 109 | a0001c0001t0001g0048a0001c0001t0001g0123a0001c0001t0001g0124others(106): Show | 109 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.319+43dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734359 | ||||||
chr22:28734825
|
G | GA | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-6-99dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734825 | ||||||
chr22:28734825
|
GA | G | 6 | a0001c0001t0001g0143a0001c0001t0001g0159a0001c0001t0001g0268others(3): Show | 6 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-99delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734825 | ||||||
chr22:28734835
|
A | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-6-108T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734835 | ||||||
chr22:28734917
|
G | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-190C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734917 | ||||||
chr22:28734965
|
G | A | 2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6-238C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734965 | ||||||
chr22:28735141
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-6-414A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735141 | ||||||
chr22:28735146
|
T | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-419A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735146 | ||||||
chr22:28735275
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-548C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735275 | ||||||
chr22:28735359
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-632A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735359 | ||||||
chr22:28735405
|
CA | C | 8 | a0001c0001t0001g0056a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-679delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735405 | ||||||
chr22:28735409
|
A | G | 1 | a0001c0002t0001g0363 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-6-682T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735409 | ||||||
chr22:28735436
|
A | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-709T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735436 | ||||||
chr22:28735438
|
T | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(123): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.-6-711A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735438 | ||||||
chr22:28735800
|
C | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-6-1073G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735800 | ||||||
chr22:28735902
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-6-1175T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735902 | ||||||
chr22:28736262
|
A | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1535T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736262 | ||||||
chr22:28736350
|
C | T | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1623G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736350 | ||||||
chr22:28736355
|
A | AC | 8 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0055others(5): Show | 8 | HG00597.hp2 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1629dupG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736355 | ||||||
chr22:28736376
|
C | A | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1649G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736376 | ||||||
chr22:28736385
|
T | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1658A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736385 | ||||||
chr22:28736401
|
G | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-6-1674C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736401 | ||||||
chr22:28736405
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-6-1678T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736405 | ||||||
chr22:28736414
|
T | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1687A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736414 | ||||||
chr22:28736470
|
T | C | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0102others(12): Show | 15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1743A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736470 | ||||||
chr22:28736526
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1799A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736526 | ||||||
chr22:28736547
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-6-1820G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736547 | ||||||
chr22:28736652
|
A | C | 2 | a0001c0002t0002g0379a0001c0002t0002g0380 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6-1925T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736652 | ||||||
chr22:28736717
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6-1990T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736717 | ||||||
chr22:28736764
|
A | AC | 19 | a0001c0001t0001g0048a0001c0001t0001g0120a0001c0001t0001g0139others(16): Show | 19 | HG00673.hp2 HG00735.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-2038dupG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736764 | ||||||
chr22:28736764
|
AC | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-6-2038delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736764 | ||||||
chr22:28736772
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-6-2045G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736772 | ||||||
chr22:28736773
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-6-2046C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736773 | ||||||
chr22:28737002
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6-2275T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737002 | ||||||
chr22:28737041
|
G | A | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0138others(11): Show | 14 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-2314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737041 | ||||||
chr22:28737045
|
G | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0104others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-6-2318C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737045 | ||||||
chr22:28737096
|
A | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | NA18983.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-6-2369T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737096 | ||||||
chr22:28737324
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0247a0001c0001t0001g0248others(5): Show | 8 | HG02056.hp2 HG02080.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-2597G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737324 | ||||||
chr22:28737334
|
A | T | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-2607T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737334 | ||||||
chr22:28737474
|
CT | C | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG01074.hp1 HG01516.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-2748delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737474 | ||||||
chr22:28737492
|
G | T | 2 | a0001c0001t0001g0346a0001c0001t0001g0362 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-6-2765C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737492 | ||||||
chr22:28737674
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-2947C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737674 | ||||||
chr22:28738014
|
T | G | 1 | a0001c0001t0001g0341 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-6-3287A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738014 | ||||||
chr22:28738315
|
C | T | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+3454G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738315 | ||||||
chr22:28738350
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01361.hp1 HG01433.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+3419C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738350 | ||||||
chr22:28738402
|
G | C | 2 | a0001c0001t0001g0342a0001c0001t0001g0343 | 2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-7+3367C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738402 | ||||||
chr22:28738497
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0136 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-7+3272T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738497 | ||||||
chr22:28738571
|
G | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.-7+3198C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738571 | ||||||
chr22:28738649
|
G | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02622.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+3120C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738649 | ||||||
chr22:28738708
|
C | A | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(8): Show | 11 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+3061G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738708 | ||||||
chr22:28738731
|
G | A | 40 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7+3038C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738731 | ||||||
chr22:28739133
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.-7+2636C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739133 | ||||||
chr22:28739208
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-7+2561C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739208 | ||||||
chr22:28739370
|
C | CT | 52 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-7+2398dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739370 | ||||||
chr22:28739532
|
T | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02622.hp2 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+2237A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739532 | ||||||
chr22:28739555
|
G | A | 40 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7+2214C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739555 | ||||||
chr22:28739901
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0123others(139): Show | 143 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-7+1868A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739901 | ||||||
chr22:28740031
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+1738T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740031 | ||||||
chr22:28740034
|
C | G | 1 | a0001c0001t0001g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7+1735G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740034 | ||||||
chr22:28740094
|
G | A | 3 | a0001c0002t0001g0344a0001c0002t0002g0379a0001c0002t0002g0380 | 3 | HG01891.hp2 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-7+1675C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740094 | ||||||
chr22:28740144
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+1625A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740144 | ||||||
chr22:28740163
|
T | A | 2 | a0001c0001t0001g0346a0001c0001t0001g0362 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-7+1606A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740163 | ||||||
chr22:28740199
|
C | CA | 5 | a0001c0001t0001g0004a0001c0001t0001g0135a0001c0001t0001g0376others(2): Show | 5 | HG01361.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1569dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740199 | ||||||
chr22:28740245
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+1524G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740245 | ||||||
chr22:28740267
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1502T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740267 | ||||||
chr22:28740532
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-7+1237T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740532 | ||||||
chr22:28740663
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7+1106G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740663 | ||||||
chr22:28740762
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1007A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740762 | ||||||
chr22:28740763
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1006C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740763 | ||||||
chr22:28740764
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1005C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740764 | ||||||
chr22:28740765
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1004T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740765 | ||||||
chr22:28740766
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1003G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740766 | ||||||
chr22:28740776
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+993A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740776 | ||||||
chr22:28740780
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+989T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740780 | ||||||
chr22:28740787
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+982T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740787 | ||||||
chr22:28740788
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-7+981G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740788 | ||||||
chr22:28740789
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+980A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740789 | ||||||
chr22:28740793
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+976G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740793 | ||||||
chr22:28740797
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+972A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740797 | ||||||
chr22:28740802
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+967G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740802 | ||||||
chr22:28740818
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+951T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740818 | ||||||
chr22:28740819
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+950T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740819 | ||||||
chr22:28740822
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+947T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740822 | ||||||
chr22:28740823
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+946C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740823 | ||||||
chr22:28740824
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+945A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740824 | ||||||
chr22:28740828
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+941C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740828 | ||||||
chr22:28740834
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+935T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740834 | ||||||
chr22:28740851
|
G | GATTCCCA others(25): Show |
1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+917_-7+918insAC others(30): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740851 | ||||||
chr22:28740878
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+891C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740878 | ||||||
chr22:28740884
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+885C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740884 | ||||||
chr22:28740892
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+877T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740892 | ||||||
chr22:28740900
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+869T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740900 | ||||||
chr22:28740909
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+860T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740909 | ||||||
chr22:28740910
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+859G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740910 | ||||||
chr22:28740919
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+850C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740919 | ||||||
chr22:28740931
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+838C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740931 | ||||||
chr22:28740954
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+815C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740954 | ||||||
chr22:28741107
|
G | A | 3 | a0001c0002t0001g0006a0001c0002t0002g0379a0001c0002t0002g0380 | 3 | HG01891.hp2 HG03516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-7+662C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741107 | ||||||
chr22:28741148
|
C | CA | 16 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(13): Show | 16 | HG00673.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7+620dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741148 | ||||||
chr22:28741148
|
CA | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG00323.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+620delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741148 | ||||||
chr22:28741169
|
A | AG | 9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG01346.hp2 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+599_-7+600insC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741169 | ||||||
chr22:28741169
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7+600T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741169 | ||||||
chr22:28741175
|
T | C | 8 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0001g0365others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+594A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741175 | ||||||
chr22:28741220
|
A | T | 1 | a0001c0002t0001g0006 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7+549T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741220 | ||||||
chr22:28741222
|
T | A | 1 | a0001c0001t0001g0371 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-7+547A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741222 | ||||||
chr22:28741228
|
T | A | 1 | a0001c0001t0001g0372 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7+541A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741228 | ||||||
chr22:28741325
|
C | A | 2 | a0001c0001t0001g0373a0001c0001t0001g0374 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-7+444G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741325 | ||||||
chr22:28741331
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+438A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741331 | ||||||
chr22:28741364
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+405C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741364 | ||||||
chr22:28741369
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+400C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741369 | ||||||
chr22:28741456
|
G | C | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0007c0010t0001g0375 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7+313C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741456 | ||||||
chr22:28741483
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0376a0001c0001t0001g0377others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+286A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741483 | ||||||
chr22:28741580
|
T | A | 1 | a0001c0001t0001g0378 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-7+189A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741580 | ||||||
chr22:28741742
|
C | G | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+27G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741742 |