geneid | 5884 |
---|---|
ensemblid | ENSG00000152942.19 |
hgncid | 9807 |
symbol | RAD17 |
name | RAD17 checkpoint clamp loader component |
refseq_nuc | NM_133338.3 |
refseq_prot | NP_579916.1 |
ensembl_nuc | ENST00000354868.10 |
ensembl_prot | ENSP00000346938.5 |
mane_status | MANE Select |
chr | chr5 |
start | 69369818 |
end | 69414801 |
strand | + |
ver | v1.2 |
region | chr5:69369818-69414801 |
region5000 | chr5:69364818-69419801 |
regionname0 | RAD17_chr5_69369818_69414801 |
regionname5000 | RAD17_chr5_69364818_69419801 |
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 | 0/1 | 670 | 264 | 68 | 48 | 118 | 6 | 23 | 93 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0002 | 0/0 | 670 | 76 | 2 | 19 | 45 | 2 | 8 | 34 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0003 | 0/0 | 670 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0004 | 0/0 | 670 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0005 | 0/0 | 670 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0006 | 0/0 | 670 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0007 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0008 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0009 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0010 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0011 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
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 | 0/1 | 2013 | 262 | 67 | 48 | 118 | 6 | 22 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0002 | 0/0 | 2013 | 76 | 2 | 19 | 45 | 2 | 8 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0003 | 0/0 | 2013 | 8 | 8 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0004 | 0/0 | 2013 | 3 | 0 | 2 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0005 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0006 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0007 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0008 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0009 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0010 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0011 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0012 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
c0013 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1042 | 268 | 50 | 55 | 133 | 7 | 22 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0002 | 0/0 | 1042 | 84 | 31 | 12 | 30 | 1 | 10 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0003 | 0/0 | 1042 | 3 | 0 | 3 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0004 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0005 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0006 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
t0007 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
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 | 0/1 | 2013 | 262 | 67 | 48 | 118 | 6 | 22 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0007 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0009 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0002c0002 | 0/0 | 2013 | 76 | 2 | 19 | 45 | 2 | 8 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0003c0003 | 0/0 | 2013 | 8 | 8 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0004c0004 | 0/0 | 2013 | 3 | 0 | 2 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0005c0005 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0006c0013 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0007c0006 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0008c0010 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0009c0008 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0010c0011 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0011c0012 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3054 | 176 | 38 | 33 | 87 | 5 | 12 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0001t0002 | 0/0 | 3054 | 80 | 28 | 12 | 29 | 1 | 10 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0001t0003 | 0/0 | 3054 | 3 | 0 | 3 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0001t0005 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0001t0006 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0001t0007 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0007t0001 | 0/0 | 3054 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0001c0009t0001 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0002c0002t0001 | 0/0 | 3054 | 76 | 2 | 19 | 45 | 2 | 8 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0003c0003t0001 | 0/0 | 3054 | 8 | 8 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0004c0004t0001 | 0/0 | 3054 | 3 | 0 | 2 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0005c0005t0002 | 0/0 | 3054 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0006c0013t0001 | 0/0 | 3054 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0007c0006t0004 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0008c0010t0002 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0009c0008t0001 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0010c0011t0002 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
a0011c0012t0001 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | copy fasta | chr5 | 69364818 | 69419801 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0009t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0005c0005t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0005c0005t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0006c0013t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0007c0006t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0008c0010t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0009c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0010c0011t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0011c0012t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0122 | EUR | GBR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0349 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01168 | hp2 | a0004 | c0004 | t0001 | g0184 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0350 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01256 | hp1 | a0006 | c0013 | t0001 | g0259 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01952 | hp2 | a0004 | c0004 | t0001 | g0183 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02896 | hp1 | a0005 | c0005 | t0002 | g0325 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02897 | hp2 | a0005 | c0005 | t0002 | g0324 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0336 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0351 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03453 | hp1 | a0008 | c0010 | t0002 | g0286 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03490 | hp1 | a0004 | c0004 | t0001 | g0128 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0331 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0216 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0348 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0347 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04204 | hp2 | a0001 | c0007 | t0001 | g0241 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18522 | hp1 | a0001 | c0009 | t0001 | g0199 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | CHB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18940 | hp2 | a0009 | c0008 | t0001 | g0158 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18977 | hp1 | a0007 | c0006 | t0004 | g0080 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19078 | hp1 | a0010 | c0011 | t0002 | g0352 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20129 | hp2 | a0011 | c0012 | t0001 | g0247 | AFR | ASW | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0155 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0313 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | GIH | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69373887
|
A | G | 1 | a0006 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.67A>G | p.Thr23Ala | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/19 | 599/3054 | 67/2013 | 23/670 | chr5 | 69373887 | ||
chr5:69373909
|
G | T | 1 | a0011 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.89G>T | p.Gly30Val | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/19 | 621/3054 | 89/2013 | 30/670 | chr5 | 69373909 | ||
chr5:69386200
|
G | A | 1 | a0007 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.719G>A | p.Arg240Gln | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1251/3054 | 719/2013 | 240/670 | chr5 | 69386200 | ||
chr5:69386217
|
A | T | 1 | a0010 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.736A>T | p.Ile246Leu | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1268/3054 | 736/2013 | 246/670 | chr5 | 69386217 | ||
chr5:69386218
|
T | A | 1 | a0010 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.737T>A | p.Ile246Lys | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1269/3054 | 737/2013 | 246/670 | chr5 | 69386218 | ||
chr5:69391965
|
G | A | 1 | a0003 | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.1141G>A | p.Val381Ile | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/19 | 1673/3054 | 1141/2013 | 381/670 | chr5 | 69391965 | ||
chr5:69393445
|
T | C | 1 | a0009 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.1367T>C | p.Ile456Thr | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/19 | 1899/3054 | 1367/2013 | 456/670 | chr5 | 69393445 | ||
chr5:69396401
|
G | T | 1 | a0005 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1427G>T | p.Arg476Leu | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/19 | 1959/3054 | 1427/2013 | 476/670 | chr5 | 69396401 | ||
chr5:69400113
|
T | G | 2 | a0002a0009 | 77 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(74): Show |
missense_variant | MODERATE | c.1637T>G | p.Leu546Arg | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/19 | 2169/3054 | 1637/2013 | 546/670 | chr5 | 69400113 | ||
chr5:69414045
|
C | T | 1 | a0008 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1766C>T | p.Ala589Val | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2298/3054 | 1766/2013 | 589/670 | chr5 | 69414045 | ||
chr5:69414057
|
G | A | 1 | a0004 | 3 | HG01168.hp2 HG01952.hp2 HG03490.hp1 |
missense_variant | MODERATE | c.1778G>A | p.Arg593Lys | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2310/3054 | 1778/2013 | 593/670 | chr5 | 69414057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69386219
|
A | T | 1 | a0010c0011 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.738A>T | p.Ile246Ile | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1270/3054 | 738/2013 | 246/670 | chr5 | 69386219 | ||
chr5:69389135
|
T | G | 1 | a0001c0007 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.996T>G | p.Ser332Ser | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/19 | 1528/3054 | 996/2013 | 332/670 | chr5 | 69389135 | ||
chr5:69414052
|
T | G | 1 | a0001c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1773T>G | p.Thr591Thr | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2305/3054 | 1773/2013 | 591/670 | chr5 | 69414052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69369909
|
T | C | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | 275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
5_prime_UTR_variant | MODIFIER | c.-441T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/19 | 2300 | chr5 | 69369909 | |||||
chr5:69371085
|
C | T | 1 | a0001c0001t0003 | 3 | HG01433.hp2 HG01496.hp2 HG01952.hp1 |
5_prime_UTR_variant | MODIFIER | c.-366C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/19 | 1124 | chr5 | 69371085 | |||||
chr5:69372154
|
T | A | 1 | a0007c0006t0004 | 1 | NA18977.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/19 | 55 | chr5 | 69372154 | |||||
chr5:69414380
|
A | G | 1 | a0001c0001t0007 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 88 | chr5 | 69414380 | |||||
chr5:69414636
|
A | G | 1 | a0001c0001t0006 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*344A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 344 | chr5 | 69414636 | |||||
chr5:69414768
|
A | C | 1 | a0001c0001t0005 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 476 | chr5 | 69414768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69369982
|
T | C | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.-417+49T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69369982 | ||||||
chr5:69370145
|
C | T | 1 | a0001c0001t0002g0354 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-417+212C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370145 | ||||||
chr5:69370156
|
G | A | 3 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-417+223G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370156 | ||||||
chr5:69370655
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-416-380T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370655 | ||||||
chr5:69370802
|
G | C | 9 | a0002c0002t0001g0007a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01975.hp2 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-416-233G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370802 | ||||||
chr5:69370855
|
G | C | 7 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0018others(4): Show | 7 | HG00558.hp2 HG02155.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-416-180G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370855 | ||||||
chr5:69370938
|
C | G | 1 | a0002c0002t0001g0271 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-416-97C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370938 | ||||||
chr5:69370958
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-416-77A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370958 | ||||||
chr5:69371436
|
T | TC | 28 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0328others(25): Show | 28 | HG00609.hp1 HG00642.hp1 HG01243.hp1 others(25): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-279-3dupC | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | |||||
chr5:69371436
|
TCC | T | 31 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(28): Show | 32 | HG00423.hp1 HG00733.hp1 HG00741.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.-279-4_-279-3delCC | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | |||||
chr5:69371436
|
TCCC | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
splice_region_variant&intron_variant | LOW | c.-279-5_-279-3delCC others(1): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | |||||
chr5:69371448
|
C | A | 8 | a0002c0002t0001g0023a0003c0003t0001g0001a0003c0003t0001g0024others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.-279-6C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | chr5 | 69371448 | ||||||
chr5:69371576
|
G | A | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-176+19G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371576 | ||||||
chr5:69371796
|
G | A | 9 | a0002c0002t0001g0007a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01975.hp2 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-175-238G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371796 | ||||||
chr5:69371979
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-175-55C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371979 | ||||||
chr5:69372377
|
C | T | 2 | a0005c0005t0002g0324a0005c0005t0002g0325 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.9+160C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372377 | ||||||
chr5:69372395
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9+178C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372395 | ||||||
chr5:69372559
|
A | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0218a0001c0001t0001g0219others(25): Show | 29 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.9+342A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372559 | ||||||
chr5:69372704
|
C | T | 1 | a0003c0003t0001g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9+487C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372704 | ||||||
chr5:69372840
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.9+623G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372840 | ||||||
chr5:69372944
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.9+727T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372944 | ||||||
chr5:69373165
|
T | C | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.10-665T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373165 | ||||||
chr5:69373422
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.10-408G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373422 | ||||||
chr5:69373431
|
G | C | 1 | a0003c0003t0001g0001 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.10-399G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373431 | ||||||
chr5:69373443
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.10-387T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373443 | ||||||
chr5:69373628
|
T | G | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10-202T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373628 | ||||||
chr5:69373663
|
G | A | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.10-167G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373663 | ||||||
chr5:69373684
|
AAATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-145_10-134delAA others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373684 | ||||||
chr5:69373685
|
AATTTT | A | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0246others(15): Show | 18 | HG00423.hp1 HG00733.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.10-144_10-140delAT others(3): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | ||||||
chr5:69373685
|
AATTTTT | A | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 140 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.10-144_10-139delAT others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | ||||||
chr5:69373685
|
AATTTTTT | A | 16 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(13): Show | 16 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.10-144_10-138delAT others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | ||||||
chr5:69373686
|
A | AT | 13 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0318others(10): Show | 13 | HG01243.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.10-114dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | |||||
chr5:69373686
|
AT | A | 14 | a0001c0001t0001g0275a0001c0001t0002g0005a0001c0001t0002g0272others(11): Show | 15 | HG00741.hp1 HG01256.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.10-114delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | |||||
chr5:69373686
|
ATT | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00621.hp1 HG02071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-115_10-114delTT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | |||||
chr5:69373686
|
ATTT | A | 82 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-116_10-114delTT others(1): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | |||||
chr5:69373686
|
ATTTT | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG00323.hp1 HG01168.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.10-117_10-114delTT others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | |||||
chr5:69373717
|
A | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.10-113A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373717 | ||||||
chr5:69374108
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267+21A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374108 | ||||||
chr5:69374112
|
C | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.267+25C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374112 | ||||||
chr5:69374223
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.267+136T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374223 | ||||||
chr5:69374274
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.267+187A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374274 | ||||||
chr5:69374312
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.267+225G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374312 | ||||||
chr5:69374530
|
A | C | 1 | a0001c0001t0005g0239 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.268-98A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374530 | ||||||
chr5:69374586
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.268-42C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374586 | ||||||
chr5:69375033
|
C | G | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+322C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375033 | ||||||
chr5:69375157
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0207others(6): Show | 10 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+446A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375157 | ||||||
chr5:69375215
|
A | T | 1 | a0001c0001t0002g0317 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.351+504A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375215 | ||||||
chr5:69375626
|
G | GTC | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.351+917_351+918dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69375626 | |||||
chr5:69375630
|
G | C | 1 | a0002c0002t0001g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.351+919G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375630 | ||||||
chr5:69375638
|
A | T | 1 | a0002c0002t0001g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.351+927A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375638 | ||||||
chr5:69375759
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+1048T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375759 | ||||||
chr5:69375855
|
T | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+1144T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375855 | ||||||
chr5:69376088
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0238 | 4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1377C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376088 | ||||||
chr5:69376089
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.351+1378G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376089 | ||||||
chr5:69376142
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+1431A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376142 | ||||||
chr5:69376332
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.351+1621G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376332 | ||||||
chr5:69376334
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+1623C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376334 | ||||||
chr5:69376486
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+1775A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376486 | ||||||
chr5:69376569
|
A | G | 1 | a0008c0010t0002g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+1858A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376569 | ||||||
chr5:69376685
|
G | C | 1 | a0002c0002t0001g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.351+1974G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376685 | ||||||
chr5:69376762
|
C | CT | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.351+2061dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69376762 | |||||
chr5:69376913
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2202G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376913 | ||||||
chr5:69376916
|
G | C | 1 | a0001c0001t0002g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.351+2205G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376916 | ||||||
chr5:69376985
|
C | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2274C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376985 | ||||||
chr5:69376999
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+2288C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376999 | ||||||
chr5:69377122
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.351+2411A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377122 | ||||||
chr5:69377288
|
A | G | 1 | a0002c0002t0001g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.351+2577A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377288 | ||||||
chr5:69377339
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(165): Show | 172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.351+2628T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377339 | ||||||
chr5:69377343
|
A | G | 4 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(1): Show | 4 | HG02165.hp2 NA18994.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2632A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377343 | ||||||
chr5:69377415
|
G | GTA | 14 | a0001c0001t0001g0135a0001c0001t0001g0197a0001c0001t0001g0245others(11): Show | 15 | HG00558.hp1 HG00733.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.351+2708_351+2709d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377415 | |||||
chr5:69377419
|
A | ATATG | 7 | a0001c0001t0001g0198a0001c0001t0001g0234a0001c0001t0001g0258others(4): Show | 7 | HG01496.hp2 HG01975.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2709_351+2710i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377419 | |||||
chr5:69377419
|
ATG | A | 9 | a0001c0001t0002g0280a0001c0001t0002g0288a0001c0001t0002g0291others(6): Show | 9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2728_351+2729d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377419 | |||||
chr5:69377421
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(147): Show | 153 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.351+2710G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377421 | ||||||
chr5:69377437
|
G | GTATA | 3 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0002g0294 | 3 | HG02895.hp2 HG02897.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.351+2727_351+2728i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
G | GTATATAT others(13): Show |
12 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0307others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+2727_351+2728i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0002g0312 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.351+2727_351+2728i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.351+2727_351+2728i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
GTGTA | G | 3 | a0001c0001t0001g0270a0001c0001t0002g0289a0001c0001t0002g0333 | 3 | HG02572.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.351+2728_351+2731d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
GTGTATA | G | 5 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0290others(2): Show | 5 | HG01243.hp1 HG01261.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2728_351+2733d others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
GTGTATAT others(5): Show |
G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+2728_351+2739d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
GTGTATAT others(9): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.351+2728_351+2743d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377437
|
GTGTATAT others(11): Show |
G | 1 | a0001c0001t0002g0326 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.351+2728_351+2745d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | |||||
chr5:69377439
|
G | A | 49 | a0001c0001t0002g0005a0001c0001t0002g0272a0001c0001t0002g0273others(46): Show | 50 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.351+2728G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377439 | ||||||
chr5:69377439
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0001g0248 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.351+2747_351+2764d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377439 | |||||
chr5:69377441
|
A | ATATATAT others(11): Show |
15 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0301others(12): Show | 15 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377441 | |||||
chr5:69377441
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(148): Show | 154 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.351+2730A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377441 | ||||||
chr5:69377443
|
A | ATATATAT others(9): Show |
6 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0317others(3): Show | 6 | HG01943.hp2 HG02155.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377443 | |||||
chr5:69377443
|
A | G | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2732A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377443 | ||||||
chr5:69377445
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0337 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.351+2749_351+2750i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377445 | |||||
chr5:69377445
|
A | ATATATAT others(7): Show |
6 | a0001c0001t0002g0005a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 7 | HG01109.hp2 HG03579.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377445 | |||||
chr5:69377450
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0258a0001c0001t0003g0269a0002c0002t0001g0007others(1): Show | 4 | HG01496.hp2 HG01975.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2740_351+2741i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | |||||
chr5:69377450
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0135a0001c0001t0001g0198 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.351+2740_351+2741i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | |||||
chr5:69377450
|
T | TATACACA others(3): Show |
3 | a0002c0002t0001g0020a0002c0002t0001g0023a0002c0002t0001g0196 | 3 | HG02155.hp2 NA18948.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | |||||
chr5:69377450
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0297 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.351+2747_351+2748i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | |||||
chr5:69377452
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2741T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377452 | ||||||
chr5:69377452
|
T | TATATATG others(19): Show |
2 | a0001c0001t0002g0296a0001c0001t0002g0321 | 2 | HG02148.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.351+2747_351+2748i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377452 | |||||
chr5:69377453
|
A | ACACACAC others(65): Show |
5 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(2): Show | 6 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2742_351+2743i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | ||||||
chr5:69377453
|
A | ACACACAC others(63): Show |
1 | a0003c0003t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.351+2742_351+2743i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | ||||||
chr5:69377453
|
A | ACACACAC others(21): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | ||||||
chr5:69377453
|
A | ACACACAC others(63): Show |
3 | a0001c0001t0001g0234a0001c0009t0001g0199a0002c0002t0001g0200 | 3 | NA18522.hp1 NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | ||||||
chr5:69377453
|
A | ATACACAC others(65): Show |
1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377453 | |||||
chr5:69377453
|
A | ATATATGT others(65): Show |
1 | a0001c0001t0002g0354 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.351+2747_351+2748i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377453 | |||||
chr5:69377454
|
T | TACACAC | 6 | a0001c0001t0001g0192a0001c0001t0001g0255a0002c0002t0001g0136others(3): Show | 6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2744_351+2745i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377454 | |||||
chr5:69377454
|
T | TATATGTA others(17): Show |
1 | a0001c0001t0002g0295 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.351+2747_351+2748i others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377454 | |||||
chr5:69377455
|
A | ACACACAC others(33): Show |
1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(42): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377455
|
A | ACACACAC others(63): Show |
1 | a0002c0002t0001g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377455
|
A | ACACACAC others(63): Show |
1 | a0002c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377455
|
A | ACACACAC others(63): Show |
138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 141 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377455
|
A | ACACACAC others(117): Show |
1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377455
|
A | ACACACAC others(65): Show |
1 | a0002c0002t0001g0013 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | ||||||
chr5:69377456
|
T | C | 6 | a0001c0001t0001g0192a0001c0001t0001g0255a0002c0002t0001g0136others(3): Show | 6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2745T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377456 | ||||||
chr5:69377456
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.351+2747_351+2766d others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377456 | |||||
chr5:69377458
|
T | TAC | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2748_351+2749i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377458 | |||||
chr5:69377458
|
TATATATA others(11): Show |
T | 79 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.351+2749_351+2766d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377458 | |||||
chr5:69377459
|
A | ACG | 9 | a0001c0001t0001g0135a0001c0001t0001g0198a0001c0001t0001g0258others(6): Show | 9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2748_351+2749i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377459 | ||||||
chr5:69377460
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2749T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377460 | ||||||
chr5:69377460
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2751_351+2766d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377460 | |||||
chr5:69377460
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+2751_351+2768d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377460 | |||||
chr5:69377462
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2751T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377462 | ||||||
chr5:69377463
|
A | G | 14 | a0001c0001t0001g0234a0001c0001t0001g0245a0001c0001t0001g0246others(11): Show | 15 | HG00733.hp1 HG01256.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+2752A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377463 | ||||||
chr5:69377464
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2753T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377464 | ||||||
chr5:69377464
|
TATATATA others(195): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2764_351+2965d others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377464 | |||||
chr5:69377465
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(149): Show | 156 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.351+2754A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377465 | ||||||
chr5:69377466
|
T | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(13): Show | 16 | HG00609.hp2 HG01099.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+2755T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377466 | ||||||
chr5:69377467
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.351+2756A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377467 | ||||||
chr5:69377468
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2757T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377468 | ||||||
chr5:69377469
|
A | G | 9 | a0001c0001t0001g0135a0001c0001t0001g0198a0001c0001t0001g0258others(6): Show | 9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2758A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377469 | ||||||
chr5:69377470
|
T | C | 6 | a0001c0001t0001g0270a0001c0001t0002g0288a0001c0001t0002g0318others(3): Show | 6 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2759T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377470 | ||||||
chr5:69377472
|
T | C | 10 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0270others(7): Show | 10 | HG02258.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+2761T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377472 | ||||||
chr5:69377473
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2762A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377473 | ||||||
chr5:69377474
|
T | C | 14 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0270others(11): Show | 14 | HG00642.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.351+2763T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377474 | ||||||
chr5:69377474
|
T | TATAC | 6 | a0001c0001t0002g0272a0001c0001t0002g0287a0001c0001t0002g0293others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2764_351+2765i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377474 | |||||
chr5:69377475
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00733.hp1 HG02895.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.351+2764A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377475 | ||||||
chr5:69377476
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.351+2765C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377476 | ||||||
chr5:69377477
|
A | G | 27 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 28 | HG00609.hp2 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.351+2766A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377477 | ||||||
chr5:69377478
|
C | T | 39 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(36): Show | 40 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.351+2767C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377478 | ||||||
chr5:69377479
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.351+2768A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377479 | ||||||
chr5:69377480
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(176): Show | 183 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.351+2769C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377480 | ||||||
chr5:69377482
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(176): Show | 183 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.351+2771C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377482 | ||||||
chr5:69377483
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2772A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377483 | ||||||
chr5:69377484
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(176): Show | 183 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.351+2773C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377484 | ||||||
chr5:69377485
|
A | ATGTG | 9 | a0001c0001t0001g0135a0001c0001t0001g0198a0001c0001t0001g0258others(6): Show | 9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2774_351+2775i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377485 | ||||||
chr5:69377485
|
A | G | 2 | a0001c0001t0001g0240a0003c0003t0001g0028 | 2 | HG01884.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.351+2774A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377485 | ||||||
chr5:69377486
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(174): Show | 181 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.351+2775C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377486 | ||||||
chr5:69377487
|
A | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 29 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+2776A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377487 | ||||||
chr5:69377488
|
T | C | 86 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(83): Show | 86 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.351+2777T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377488 | ||||||
chr5:69377489
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(137): Show | 143 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.351+2778A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377489 | ||||||
chr5:69377495
|
A | G | 18 | a0001c0001t0001g0192a0001c0001t0001g0234a0001c0001t0001g0255others(15): Show | 19 | HG00609.hp2 HG01256.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.351+2784A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377495 | ||||||
chr5:69377496
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 165 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.351+2785C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377496 | ||||||
chr5:69377499
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(137): Show | 143 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.351+2788A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377499 | ||||||
chr5:69377499
|
ATATATAT others(155): Show |
A | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2793_351+2954d others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377499 | |||||
chr5:69377505
|
A | ATG | 3 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0106 | 3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2796_351+2797d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377505 | |||||
chr5:69377505
|
A | G | 4 | a0001c0001t0001g0234a0001c0009t0001g0199a0002c0002t0001g0013others(1): Show | 4 | NA18522.hp1 NA18946.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2794A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377505 | ||||||
chr5:69377506
|
T | C | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2795T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377506 | ||||||
chr5:69377506
|
T | TAC | 7 | a0001c0001t0001g0192a0001c0001t0001g0255a0002c0002t0001g0136others(4): Show | 7 | HG00609.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2795_351+2796i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377506 | ||||||
chr5:69377507
|
G | GTA | 4 | a0001c0001t0001g0234a0001c0009t0001g0199a0002c0002t0001g0013others(1): Show | 4 | NA18522.hp1 NA18946.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2803_351+2804d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377507 | |||||
chr5:69377507
|
G | GTGTA | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 153 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.351+2797_351+2798i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377507 | |||||
chr5:69377509
|
A | ATATATAT others(57): Show |
6 | a0001c0001t0001g0135a0001c0001t0001g0198a0001c0001t0001g0258others(3): Show | 6 | HG01496.hp2 HG01975.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2804_351+2805i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | |||||
chr5:69377509
|
A | ATATATAT others(59): Show |
1 | a0002c0002t0001g0196 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.351+2804_351+2805i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | |||||
chr5:69377509
|
A | ATATATAT others(55): Show |
2 | a0002c0002t0001g0020a0002c0002t0001g0023 | 2 | HG02155.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.351+2804_351+2805i others(64): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | |||||
chr5:69377516
|
C | T | 18 | a0001c0001t0001g0135a0001c0001t0001g0192a0001c0001t0001g0198others(15): Show | 18 | HG00609.hp2 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.351+2805C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377516 | ||||||
chr5:69377519
|
A | ATATATG | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(142): Show | 148 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.351+2813_351+2814i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377519 | |||||
chr5:69377525
|
A | ATGTATAT others(3): Show |
6 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(3): Show | 7 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2817_351+2818i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377525 | |||||
chr5:69377525
|
A | G | 11 | a0001c0001t0001g0135a0001c0001t0001g0198a0001c0001t0001g0240others(8): Show | 11 | HG01496.hp2 HG01884.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2814A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377525 | ||||||
chr5:69377527
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2817_351+2818i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377527 | |||||
chr5:69377528
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0106 | 3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2817T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377528 | ||||||
chr5:69377529
|
G | A | 22 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0106others(19): Show | 23 | HG00733.hp1 HG01099.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.351+2818G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377529 | ||||||
chr5:69377529
|
G | GTA | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(147): Show | 153 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.351+2825_351+2826d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377529 | |||||
chr5:69377538
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0106 | 3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2827C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377538 | ||||||
chr5:69377540
|
T | TATAC | 3 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0106 | 3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2832_351+2833i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | |||||
chr5:69377540
|
T | TATATATA others(97): Show |
1 | a0001c0001t0001g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.351+2837_351+2838i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | |||||
chr5:69377540
|
T | TATATATA others(95): Show |
8 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0101others(5): Show | 8 | HG01168.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2847_351+2848i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | |||||
chr5:69377550
|
C | CAT | 108 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0037others(105): Show | 110 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.351+2846_351+2847d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377550 | |||||
chr5:69377550
|
C | T | 7 | a0001c0001t0001g0192a0001c0001t0001g0255a0002c0002t0001g0136others(4): Show | 7 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2839C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377550 | ||||||
chr5:69377554
|
T | C | 2 | a0001c0001t0001g0207a0002c0002t0001g0138 | 2 | NA18952.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.351+2843T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377554 | ||||||
chr5:69377555
|
A | ATGTGTAT others(107): Show |
1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2845_351+2846i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377555 | |||||
chr5:69377557
|
A | G | 6 | a0001c0001t0001g0192a0001c0001t0001g0255a0002c0002t0001g0136others(3): Show | 6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2846A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377557 | ||||||
chr5:69377558
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0002g0313 | 2 | HG03834.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.351+2847T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377558 | ||||||
chr5:69377559
|
G | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 7 | HG01243.hp2 NA18956.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2848G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377559 | ||||||
chr5:69377559
|
GTA | G | 9 | a0001c0001t0002g0288a0001c0001t0002g0291a0001c0001t0002g0293others(6): Show | 9 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2858_351+2859d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377559 | |||||
chr5:69377560
|
T | C | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2849T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377560 | ||||||
chr5:69377560
|
T | TATAC | 6 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0245others(3): Show | 6 | HG00733.hp1 HG01099.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2852_351+2853i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377560 | |||||
chr5:69377560
|
T | TATATATG others(121): Show |
1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+2855_351+2856i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377560 | |||||
chr5:69377562
|
T | TAC | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.351+2852_351+2853i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | |||||
chr5:69377562
|
T | TATATGTG others(103): Show |
2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG02559.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.351+2855_351+2856i others(112): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | |||||
chr5:69377562
|
T | TATATGTG others(101): Show |
3 | a0001c0001t0001g0192a0002c0002t0001g0189a0002c0002t0001g0190 | 3 | HG00609.hp2 NA18980.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.351+2855_351+2856i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | |||||
chr5:69377562
|
T | TGTATAC | 5 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2851_351+2852i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377562 | ||||||
chr5:69377572
|
C | CAT | 4 | a0001c0001t0001g0056a0001c0001t0001g0106a0001c0001t0001g0255others(1): Show | 4 | HG02155.hp2 HG02280.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2868_351+2869d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377572 | |||||
chr5:69377572
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2861C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377572 | ||||||
chr5:69377585
|
A | ACATATAT others(31): Show |
1 | a0001c0001t0002g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(40): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377585 | |||||
chr5:69377585
|
A | G | 12 | a0001c0001t0001g0131a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG00609.hp2 HG00733.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+2874A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377585 | ||||||
chr5:69377586
|
C | CAT | 8 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0101others(5): Show | 8 | HG01168.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2884_351+2885d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
C | CATATATA others(99): Show |
1 | a0001c0001t0001g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.351+2885_351+2886i others(108): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
C | CATATATA others(97): Show |
21 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(18): Show | 21 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
C | CATATATA others(99): Show |
1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(108): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
C | CATATATA others(95): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | HG04204.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
CAT | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0135a0001c0001t0001g0139others(5): Show | 8 | HG01099.hp2 HG01243.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+2884_351+2885d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377586
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2879_351+2902d others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | |||||
chr5:69377587
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377587 | |||||
chr5:69377587
|
A | C | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2876A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377587 | ||||||
chr5:69377588
|
T | TATATATA others(95): Show |
3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02572.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | |||||
chr5:69377588
|
T | TATATATA others(67): Show |
1 | a0001c0001t0001g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | |||||
chr5:69377588
|
T | TATATATA others(93): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0119 | 2 | HG00741.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(102): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | |||||
chr5:69377588
|
T | TATATATG others(87): Show |
1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.351+2883_351+2884i others(96): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | |||||
chr5:69377588
|
T | TATATATG others(85): Show |
1 | a0002c0002t0001g0130 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.351+2883_351+2884i others(94): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | |||||
chr5:69377593
|
A | ATATGCAT others(97): Show |
1 | a0001c0001t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377593 | |||||
chr5:69377593
|
A | ATGCATAT others(5): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377593 | |||||
chr5:69377594
|
T | TATGCATA others(59): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0207others(5): Show | 9 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(87): Show |
1 | a0001c0001t0001g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(96): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(95): Show |
1 | a0002c0002t0001g0022 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(237): Show |
1 | a0002c0002t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(131): Show |
1 | a0002c0002t0001g0012 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(140): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(143): Show |
1 | a0001c0001t0001g0193 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(143): Show |
37 | a0001c0001t0001g0131a0001c0001t0001g0194a0001c0001t0001g0195others(34): Show | 38 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(185): Show |
1 | a0002c0002t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(194): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(171): Show |
5 | a0002c0002t0001g0013a0002c0002t0001g0122a0002c0002t0001g0146others(2): Show | 5 | HG00099.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(180): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(129): Show |
1 | a0002c0002t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(138): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(195): Show |
1 | a0002c0002t0001g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(204): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(227): Show |
1 | a0002c0002t0001g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(236): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(169): Show |
2 | a0002c0002t0001g0124a0002c0002t0001g0163 | 2 | NA18981.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(178): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(121): Show |
1 | a0001c0001t0001g0167 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(141): Show |
1 | a0001c0001t0001g0182 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(169): Show |
1 | a0001c0001t0003g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(178): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TATGCATA others(143): Show |
1 | a0002c0002t0001g0007 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.351+2893_351+2894i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | |||||
chr5:69377594
|
T | TGCATATA others(141): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | ||||||
chr5:69377594
|
T | TGCATATA others(207): Show |
1 | a0002c0002t0001g0120 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(216): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | ||||||
chr5:69377594
|
T | TGCATATA others(141): Show |
3 | a0001c0001t0001g0191a0002c0002t0001g0030a0002c0002t0001g0031 | 3 | HG01346.hp1 HG01358.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | ||||||
chr5:69377598
|
CAT | C | 65 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0038others(62): Show | 66 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.351+2896_351+2897d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377598 | |||||
chr5:69377600
|
T | TATATATG others(1): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0125others(31): Show | 34 | HG00323.hp2 HG00558.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377600
|
T | TATATATG others(27): Show |
1 | a0002c0002t0001g0138 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(36): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377600
|
T | TATATATG others(51): Show |
12 | a0002c0002t0001g0011a0002c0002t0001g0020a0002c0002t0001g0144others(9): Show | 12 | HG00423.hp1 HG01928.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(60): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377600
|
T | TATATATG others(43): Show |
1 | a0001c0001t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(52): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377600
|
T | TATATATG others(41): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0103 | 2 | HG00735.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(50): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377600
|
T | TATATATG others(133): Show |
1 | a0001c0001t0001g0042 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(142): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | |||||
chr5:69377604
|
T | TATGTATA others(107): Show |
1 | a0001c0001t0001g0047 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377604 | |||||
chr5:69377607
|
A | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+2896A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377607 | ||||||
chr5:69377609
|
G | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0064others(8): Show | 11 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2898G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377609 | ||||||
chr5:69377610
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0132others(64): Show | 69 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.351+2899T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377610 | ||||||
chr5:69377612
|
T | C | 10 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+2901T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377612 | ||||||
chr5:69377613
|
A | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0047others(31): Show | 34 | HG00323.hp2 HG00558.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.351+2902A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377613 | ||||||
chr5:69377614
|
C | CAT | 9 | a0001c0001t0001g0042a0001c0001t0001g0135a0001c0001t0001g0139others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2910_351+2911d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(37): Show |
1 | a0001c0001t0001g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(46): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(115): Show |
1 | a0001c0001t0001g0052 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(124): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(97): Show |
1 | a0001c0001t0001g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.351+2911_351+2912i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(83): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2911_351+2912i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(113): Show |
1 | a0001c0001t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.351+2911_351+2912i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(111): Show |
18 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0053others(15): Show | 18 | HG00099.hp2 HG00438.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.351+2911_351+2912i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(109): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02132.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(118): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(109): Show |
1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(118): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(107): Show |
3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0113 | 3 | HG03139.hp2 NA19058.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(5): Show |
38 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.351+2910_351+2921d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(57): Show |
1 | a0001c0001t0002g0349 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | CATATATA others(81): Show |
1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | |||||
chr5:69377614
|
C | T | 11 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2903C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377614 | ||||||
chr5:69377619
|
A | ATG | 4 | a0001c0001t0001g0208a0001c0001t0003g0217a0002c0002t0001g0013others(1): Show | 4 | HG01433.hp2 HG03834.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2909_351+2910i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377619 | |||||
chr5:69377620
|
T | TATATGCA others(249): Show |
2 | a0001c0001t0001g0198a0001c0009t0001g0199 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(258): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377620 | |||||
chr5:69377620
|
T | TGC | 67 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0132others(64): Show | 69 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.351+2909_351+2910i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377620 | ||||||
chr5:69377623
|
G | GCATATAT others(75): Show |
1 | a0001c0001t0002g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.351+2921_351+2922i others(84): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | |||||
chr5:69377623
|
G | GCATATAT others(73): Show |
1 | a0001c0001t0002g0315 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(82): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | |||||
chr5:69377623
|
GCATATAT others(7): Show |
G | 1 | a0001c0001t0002g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351+2922_351+2935d others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | |||||
chr5:69377624
|
C | CAT | 74 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0001g0131others(71): Show | 76 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.351+2920_351+2921d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | |||||
chr5:69377624
|
C | CATATATA others(201): Show |
1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+2922_351+2923i others(210): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | |||||
chr5:69377624
|
C | CATATATA others(97): Show |
4 | a0001c0001t0002g0342a0001c0001t0002g0343a0001c0001t0002g0344others(1): Show | 4 | NA18960.hp2 NA18997.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | |||||
chr5:69377624
|
C | CATATATA others(89): Show |
1 | a0001c0001t0001g0142 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.351+2925_351+2926i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | |||||
chr5:69377626
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.351+2921_351+2922i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377626 | |||||
chr5:69377628
|
T | TATATATA others(67): Show |
2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.351+2921_351+2922i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377628 | |||||
chr5:69377628
|
T | TATATATG others(17): Show |
2 | a0001c0001t0001g0275a0001c0001t0002g0333 | 2 | HG00741.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.351+2921_351+2922i others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377628 | |||||
chr5:69377632
|
T | TGCATACA others(5): Show |
1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2922_351+2923i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377632 | |||||
chr5:69377633
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0002g0276a0001c0001t0002g0277others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2922G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377633 | ||||||
chr5:69377634
|
T | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 5 | HG01346.hp1 HG01358.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2923T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377634 | ||||||
chr5:69377637
|
A | ACATATAT others(5): Show |
2 | a0001c0001t0001g0270a0001c0001t0002g0349 | 2 | HG00642.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.351+2939_351+2950d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(71): Show |
1 | a0001c0001t0002g0290 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.351+2977_351+2978i others(80): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(57): Show |
1 | a0001c0001t0002g0294 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.351+2975_351+2976i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(121): Show |
1 | a0008c0010t0002g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+2963_351+2964i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(71): Show |
2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(80): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(69): Show |
1 | a0001c0001t0002g0348 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(78): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(57): Show |
2 | a0001c0001t0002g0318a0001c0001t0002g0332 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(69): Show |
40 | a0001c0001t0002g0005a0001c0001t0002g0278a0001c0001t0002g0279others(37): Show | 41 | HG00609.hp1 HG01256.hp2 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(78): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(29): Show |
3 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0338 | 3 | HG04184.hp1 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(38): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(119): Show |
12 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0002g0287others(9): Show | 12 | HG01243.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(128): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(145): Show |
1 | a0001c0001t0002g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(154): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(67): Show |
5 | a0001c0001t0002g0281a0001c0001t0002g0312a0001c0001t0002g0319others(2): Show | 5 | HG02965.hp2 HG03540.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(107): Show |
1 | a0001c0001t0002g0309 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(159): Show |
1 | a0001c0001t0001g0095 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(168): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(81): Show |
1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | ACATATAT others(117): Show |
1 | a0001c0001t0002g0272 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.351+2933_351+2934i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | |||||
chr5:69377637
|
A | G | 4 | a0001c0001t0001g0275a0001c0001t0002g0276a0001c0001t0002g0277others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2926A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377637 | ||||||
chr5:69377639
|
A | G | 1 | a0003c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+2928A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377639 | ||||||
chr5:69377640
|
T | TATATATA others(149): Show |
1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+2937_351+2938i others(158): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | |||||
chr5:69377640
|
T | TATATATA others(177): Show |
1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2937_351+2938i others(186): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | |||||
chr5:69377640
|
T | TATATATA others(59): Show |
1 | a0001c0001t0002g0314 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | |||||
chr5:69377645
|
A | ATGCATAT others(91): Show |
1 | a0001c0001t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(100): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(89): Show |
1 | a0002c0002t0001g0020 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(89): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0125a0001c0001t0001g0126others(2): Show | 5 | HG00323.hp2 HG01070.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(75): Show |
1 | a0002c0002t0001g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(84): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(113): Show |
2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG02559.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(137): Show |
1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(137): Show |
1 | a0001c0001t0001g0172 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(165): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0171a0002c0002t0001g0216 | 3 | HG03927.hp2 NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(174): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(137): Show |
11 | a0001c0001t0001g0032a0001c0001t0001g0175a0001c0001t0001g0177others(8): Show | 11 | HG01167.hp1 HG02074.hp2 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(135): Show |
3 | a0004c0004t0001g0128a0004c0004t0001g0183a0004c0004t0001g0184 | 3 | HG01168.hp2 HG01952.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(144): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(137): Show |
1 | a0001c0001t0001g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | ATGCATAT others(137): Show |
3 | a0001c0001t0003g0267a0001c0001t0003g0269a0002c0002t0001g0186 | 3 | HG01496.hp2 HG01952.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | |||||
chr5:69377645
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0132others(73): Show | 78 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.351+2934A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377645 | ||||||
chr5:69377646
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2935T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TATGCATA others(239): Show |
1 | a0001c0001t0001g0220 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(239): Show |
2 | a0001c0001t0001g0222a0001c0001t0001g0242 | 2 | NA18954.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(263): Show |
1 | a0001c0001t0001g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(263): Show |
7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | NA18949.hp2 NA18955.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(261): Show |
1 | a0001c0001t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(270): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(239): Show |
2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(293): Show |
1 | a0001c0001t0001g0229 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(302): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(211): Show |
1 | a0001c0001t0001g0262 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(220): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(239): Show |
1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(267): Show |
1 | a0001c0001t0005g0239 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(263): Show |
1 | a0001c0001t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TATGCATA others(237): Show |
1 | a0001c0001t0001g0235 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | |||||
chr5:69377646
|
T | TGCATATA others(89): Show |
3 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0145 | 3 | HG01074.hp1 HG03688.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(117): Show |
1 | a0002c0002t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(117): Show |
1 | a0002c0002t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(89): Show |
7 | a0001c0001t0001g0165a0001c0001t0001g0166a0002c0002t0001g0149others(4): Show | 7 | HG00423.hp1 HG01978.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(101): Show |
1 | a0002c0002t0001g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(125): Show |
1 | a0002c0002t0001g0011 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(134): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(113): Show |
1 | a0002c0002t0001g0138 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(237): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0238 | 4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(261): Show |
1 | a0001c0001t0001g0230 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(270): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(237): Show |
1 | a0001c0001t0001g0231 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(235): Show |
1 | a0001c0001t0001g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(244): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(113): Show |
2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG00609.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(111): Show |
1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(137): Show |
1 | a0001c0001t0001g0170 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377646
|
T | TGCATATA others(137): Show |
1 | a0001c0001t0001g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | ||||||
chr5:69377650
|
C | CAT | 79 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.351+2948_351+2949d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | |||||
chr5:69377650
|
C | CATATATA others(111): Show |
1 | a0001c0001t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | |||||
chr5:69377650
|
CAT | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0118others(1): Show | 4 | HG01099.hp2 HG01978.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2948_351+2949d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | |||||
chr5:69377652
|
T | TATATATA others(29): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0103 | 2 | HG00735.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.351+2963_351+2964i others(38): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | |||||
chr5:69377652
|
T | TATATATG others(83): Show |
1 | a0001c0001t0001g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | |||||
chr5:69377652
|
T | TATATATG others(81): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00642.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | |||||
chr5:69377652
|
T | TATATATG others(107): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0249 | 2 | HG02080.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | |||||
chr5:69377654
|
T | C | 2 | a0001c0001t0002g0337a0003c0003t0001g0028 | 2 | HG01884.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.351+2943T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377654 | ||||||
chr5:69377660
|
T | C | 1 | a0003c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+2949T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377660 | ||||||
chr5:69377660
|
T | G | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2949T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377660 | ||||||
chr5:69377661
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2950G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377661 | ||||||
chr5:69377662
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2951T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377662 | ||||||
chr5:69377663
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2952A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377663 | ||||||
chr5:69377665
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0007t0001g0241others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2954A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377665 | ||||||
chr5:69377666
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2955C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377666 | ||||||
chr5:69377667
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2956A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377667 | ||||||
chr5:69377668
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2957T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377668 | ||||||
chr5:69377668
|
T | TATATATG others(19): Show |
1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+2963_351+2964i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377668 | |||||
chr5:69377670
|
T | TATATGCA others(249): Show |
1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.351+2963_351+2964i others(258): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377670 | |||||
chr5:69377671
|
A | ATATGTAT others(101): Show |
1 | a0003c0003t0001g0001 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+2963_351+2964i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377671 | |||||
chr5:69377671
|
A | G | 2 | a0001c0001t0001g0049a0006c0013t0001g0259 | 2 | HG01256.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.351+2960A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377671 | ||||||
chr5:69377673
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.351+2962A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377673 | ||||||
chr5:69377674
|
T | C | 1 | a0002c0002t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.351+2963T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377674 | ||||||
chr5:69377675
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2964A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377675 | ||||||
chr5:69377677
|
GCATA | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2967_351+2970d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377677 | ||||||
chr5:69377678
|
C | T | 8 | a0001c0001t0001g0049a0001c0001t0001g0135a0003c0003t0001g0001others(5): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2967C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377678 | ||||||
chr5:69377678
|
CAT | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.351+2978_351+2979d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377678 | |||||
chr5:69377678
|
CATAT | C | 64 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0039others(61): Show | 64 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.351+2976_351+2979d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377678 | |||||
chr5:69377680
|
T | TACATATA others(35): Show |
1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2970_351+2971i others(44): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TACATATA others(105): Show |
4 | a0003c0003t0001g0025a0003c0003t0001g0026a0003c0003t0001g0027others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2970_351+2971i others(114): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TACATATA others(105): Show |
1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2970_351+2971i others(114): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TATATATA others(21): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0118 | 3 | HG00735.hp1 HG01346.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.351+2996_351+2997i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TATATATA others(85): Show |
1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(94): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TATATATA others(19): Show |
2 | a0002c0002t0001g0129a0002c0002t0001g0130 | 2 | HG01074.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.351+2977_351+2978i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TATATATG others(281): Show |
1 | a0001c0001t0001g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(290): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TATATATG others(227): Show |
1 | a0001c0007t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(236): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | |||||
chr5:69377680
|
T | TGC | 2 | a0001c0001t0001g0135a0003c0003t0001g0001 | 3 | HG02258.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.351+2969_351+2970i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377680 | ||||||
chr5:69377681
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2970A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377681 | ||||||
chr5:69377682
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2971T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377682 | ||||||
chr5:69377682
|
T | TATATATA others(19): Show |
6 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00642.hp2 HG01934.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2996_351+2997i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATATG others(57): Show |
1 | a0001c0001t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATATG others(83): Show |
1 | a0001c0001t0001g0106 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATGTA others(15): Show |
1 | a0001c0001t0001g0037 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.351+2975_351+2976i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATGTA others(41): Show |
1 | a0001c0001t0001g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(50): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATGTA others(157): Show |
1 | a0001c0001t0001g0104 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(166): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATGTA others(155): Show |
1 | a0001c0001t0001g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(164): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377682
|
T | TATATGTA others(15): Show |
3 | a0002c0002t0001g0202a0002c0002t0001g0203a0002c0002t0001g0204 | 3 | NA18994.hp1 NA19004.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.351+2975_351+2976i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | |||||
chr5:69377684
|
T | C | 1 | a0002c0002t0001g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.351+2973T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377684 | ||||||
chr5:69377688
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2977T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377688 | ||||||
chr5:69377689
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2978A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377689 | ||||||
chr5:69377692
|
T | C | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2981T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377692 | ||||||
chr5:69377697
|
A | C | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2986A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377697 | ||||||
chr5:69377721
|
ATTTTC | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.351+3014_351+3018d others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377721 | |||||
chr5:69377747
|
C | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0255 | 3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.351+3036C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377747 | ||||||
chr5:69377826
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0119 | 3 | NA18979.hp2 NA19058.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.351+3115C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377826 | ||||||
chr5:69377970
|
A | T | 1 | a0003c0003t0001g0001 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+3259A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377970 | ||||||
chr5:69378086
|
C | T | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+3375C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378086 | ||||||
chr5:69378233
|
A | G | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.351+3522A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378233 | ||||||
chr5:69378359
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.352-3542G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378359 | ||||||
chr5:69378594
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.352-3307C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378594 | ||||||
chr5:69378732
|
G | T | 2 | a0001c0001t0002g0335a0001c0001t0002g0350 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.352-3169G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378732 | ||||||
chr5:69378814
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.352-3087G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378814 | ||||||
chr5:69379015
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-2886G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379015 | ||||||
chr5:69379111
|
G | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.352-2790G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379111 | ||||||
chr5:69379189
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.352-2712T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379189 | ||||||
chr5:69379316
|
C | T | 17 | a0002c0002t0001g0002a0002c0002t0001g0123a0002c0002t0001g0124others(14): Show | 18 | HG00423.hp1 HG02056.hp2 NA18939.hp1 others(15): Show |
intron_variant | MODIFIER | c.352-2585C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379316 | ||||||
chr5:69379335
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.352-2566T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379335 | ||||||
chr5:69379622
|
TTATTCTA others(50): Show |
T | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-2278_352-2222d others(59): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379622 | ||||||
chr5:69379623
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352-2278T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379623 | ||||||
chr5:69379656
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.352-2245A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379656 | ||||||
chr5:69379657
|
T | A | 1 | a0002c0002t0001g0018 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.352-2244T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379657 | ||||||
chr5:69379920
|
G | C | 1 | a0002c0002t0001g0201 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.352-1981G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379920 | ||||||
chr5:69379983
|
C | G | 1 | a0001c0001t0002g0338 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.352-1918C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379983 | ||||||
chr5:69379989
|
T | C | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1912T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379989 | ||||||
chr5:69379990
|
C | T | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1911C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379990 | ||||||
chr5:69379992
|
T | G | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1909T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379992 | ||||||
chr5:69380038
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.352-1863G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380038 | ||||||
chr5:69380068
|
A | T | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1833A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380068 | ||||||
chr5:69380069
|
T | G | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1832T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380069 | ||||||
chr5:69380073
|
G | C | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.352-1828G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380073 | ||||||
chr5:69380193
|
T | A | 1 | a0002c0002t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.352-1708T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380193 | ||||||
chr5:69380434
|
A | G | 1 | a0002c0002t0001g0268 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.352-1467A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380434 | ||||||
chr5:69380528
|
C | A | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1373C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380528 | ||||||
chr5:69380563
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.352-1338C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380563 | ||||||
chr5:69380727
|
T | C | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1174T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380727 | ||||||
chr5:69380744
|
C | T | 36 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(33): Show | 36 | HG00423.hp2 HG00621.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.352-1157C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380744 | ||||||
chr5:69380771
|
CT | C | 8 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-1118delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69380771 | |||||
chr5:69380807
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.352-1094G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380807 | ||||||
chr5:69380972
|
T | A | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-929T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380972 | ||||||
chr5:69381012
|
G | A | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.352-889G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381012 | ||||||
chr5:69381337
|
C | T | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352-564C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381337 | ||||||
chr5:69381355
|
CCTGTAGT others(125): Show |
C | 1 | a0001c0001t0002g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.352-545_352-414del | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381355 | ||||||
chr5:69381479
|
CA | C | 14 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0265others(11): Show | 15 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.352-409delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69381479 | |||||
chr5:69381521
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.352-380C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381521 | ||||||
chr5:69382304
|
G | A | 2 | a0001c0001t0003g0267a0001c0001t0003g0269 | 2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.508+247G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382304 | ||||||
chr5:69382357
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.508+300A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382357 | ||||||
chr5:69382504
|
A | G | 2 | a0001c0001t0002g0298a0001c0001t0002g0300 | 2 | HG04184.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.508+447A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382504 | ||||||
chr5:69382534
|
T | C | 1 | a0004c0004t0001g0183 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.508+477T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382534 | ||||||
chr5:69382544
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+487G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382544 | ||||||
chr5:69382721
|
A | G | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+664A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382721 | ||||||
chr5:69382764
|
G | A | 1 | a0003c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508+707G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382764 | ||||||
chr5:69382784
|
A | C | 1 | a0001c0001t0002g0341 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.508+727A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382784 | ||||||
chr5:69382838
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.508+781C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382838 | ||||||
chr5:69382890
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.508+833T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382890 | ||||||
chr5:69382959
|
T | C | 52 | a0001c0001t0002g0005a0001c0001t0002g0276a0001c0001t0002g0277others(49): Show | 53 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.508+902T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382959 | ||||||
chr5:69382983
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.508+926C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382983 | ||||||
chr5:69383003
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.508+946C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383003 | ||||||
chr5:69383038
|
C | T | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.508+981C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383038 | ||||||
chr5:69383046
|
A | T | 1 | a0001c0001t0002g0341 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.508+989A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383046 | ||||||
chr5:69383140
|
T | G | 1 | a0001c0001t0002g0005 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+1083T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383140 | ||||||
chr5:69383144
|
C | G | 1 | a0002c0002t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.508+1087C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383144 | ||||||
chr5:69383323
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508+1266A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383323 | ||||||
chr5:69383540
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.509-1257G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383540 | ||||||
chr5:69383660
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02572.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509-1137G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383660 | ||||||
chr5:69383719
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.509-1078A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383719 | ||||||
chr5:69383735
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.509-1062A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383735 | ||||||
chr5:69383766
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.509-1031C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383766 | ||||||
chr5:69383796
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509-1001G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383796 | ||||||
chr5:69383969
|
C | G | 1 | a0002c0002t0001g0216 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.509-828C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383969 | ||||||
chr5:69383995
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.509-802G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383995 | ||||||
chr5:69384005
|
A | AAAATTCA others(72): Show |
3 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0338 | 3 | HG04184.hp1 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.509-715_509-714ins others(79): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 69384005 | |||||
chr5:69384030
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.509-767G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384030 | ||||||
chr5:69384090
|
T | G | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.509-707T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384090 | ||||||
chr5:69384207
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-590T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384207 | ||||||
chr5:69384505
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-292C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384505 | ||||||
chr5:69384516
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.509-281A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384516 | ||||||
chr5:69384954
|
C | CT | 10 | a0001c0001t0001g0091a0001c0001t0001g0116a0002c0002t0001g0180others(7): Show | 11 | HG01884.hp1 HG01884.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.645+38dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69384954 | |||||
chr5:69384982
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645+49C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69384982 | ||||||
chr5:69385033
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.645+100C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385033 | ||||||
chr5:69385045
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.645+112T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385045 | ||||||
chr5:69385050
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.645+117C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385050 | ||||||
chr5:69385120
|
C | T | 2 | a0001c0001t0002g0283a0001c0001t0002g0306 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.645+187C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385120 | ||||||
chr5:69385150
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0135a0001c0001t0001g0139others(44): Show | 49 | HG00438.hp1 HG00621.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.645+217C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385150 | ||||||
chr5:69385192
|
C | A | 1 | a0002c0002t0001g0159 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.645+259C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385192 | ||||||
chr5:69385266
|
C | CT | 101 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.645+353dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | |||||
chr5:69385266
|
C | CTT | 9 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0054others(6): Show | 9 | HG01358.hp2 HG01934.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+352_645+353dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | |||||
chr5:69385266
|
CT | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0237a0001c0001t0001g0242others(6): Show | 9 | HG00323.hp2 HG00733.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+353delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | |||||
chr5:69385329
|
T | C | 2 | a0001c0001t0003g0267a0001c0001t0003g0269 | 2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.645+396T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385329 | ||||||
chr5:69385354
|
C | T | 2 | a0001c0001t0001g0263a0011c0012t0001g0247 | 2 | NA18612.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.645+421C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385354 | ||||||
chr5:69385796
|
T | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.646-247T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385796 | ||||||
chr5:69385812
|
A | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.646-231A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385812 | ||||||
chr5:69385817
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.646-226A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385817 | ||||||
chr5:69385848
|
A | C | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-195A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385848 | ||||||
chr5:69385869
|
C | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.646-174C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385869 | ||||||
chr5:69385878
|
T | A | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-165T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385878 | ||||||
chr5:69386023
|
T | A | 1 | a0010c0011t0002g0352 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-20T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69386023 | ||||||
chr5:69386646
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.894+181T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386646 | ||||||
chr5:69386709
|
A | C | 4 | a0002c0002t0001g0134a0002c0002t0001g0160a0002c0002t0001g0161others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+244A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386709 | ||||||
chr5:69386771
|
C | G | 4 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0002g0297others(1): Show | 4 | HG01261.hp2 HG02148.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+306C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386771 | ||||||
chr5:69386926
|
C | CT | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(161): Show | 167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.894+476dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69386926 | |||||
chr5:69387220
|
G | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+755G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387220 | ||||||
chr5:69387230
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.894+765C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387230 | ||||||
chr5:69387242
|
G | T | 2 | a0002c0002t0001g0147a0002c0002t0001g0162 | 2 | HG02738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.894+777G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387242 | ||||||
chr5:69387390
|
C | T | 3 | a0002c0002t0001g0122a0002c0002t0001g0146a0002c0002t0001g0148 | 3 | HG00099.hp1 HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.894+925C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387390 | ||||||
chr5:69387417
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.894+952G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387417 | ||||||
chr5:69387544
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.894+1079T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387544 | ||||||
chr5:69387610
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894+1145C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387610 | ||||||
chr5:69387641
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.894+1176T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387641 | ||||||
chr5:69387718
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.894+1253G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387718 | ||||||
chr5:69387719
|
T | G | 1 | a0001c0001t0002g0299 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.894+1254T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387719 | ||||||
chr5:69387723
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.894+1258G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387723 | ||||||
chr5:69387758
|
G | C | 1 | a0001c0001t0001g0182 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.895-1276G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387758 | ||||||
chr5:69387786
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.895-1248G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387786 | ||||||
chr5:69388011
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.895-1023A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388011 | ||||||
chr5:69388081
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.895-953A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388081 | ||||||
chr5:69388134
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.895-900C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388134 | ||||||
chr5:69388191
|
A | AT | 104 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(101): Show | 105 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.895-833dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388191 | |||||
chr5:69388228
|
T | C | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-806T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388228 | ||||||
chr5:69388233
|
T | C | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.895-801T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388233 | ||||||
chr5:69388387
|
ATTTTGAG others(5): Show |
A | 1 | a0007c0006t0004g0080 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.895-641_895-630del others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388387 | |||||
chr5:69388396
|
G | GT | 4 | a0001c0001t0002g0353a0002c0002t0001g0121a0002c0002t0001g0143others(1): Show | 4 | HG01192.hp2 HG02056.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-631dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388396 | |||||
chr5:69388492
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.895-542A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388492 | ||||||
chr5:69388611
|
C | T | 349 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(346): Show | 354 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(351): Show |
intron_variant | MODIFIER | c.895-423C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388611 | ||||||
chr5:69388643
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.895-391A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388643 | ||||||
chr5:69388645
|
T | A | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.895-389T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388645 | ||||||
chr5:69389210
|
A | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01070.hp2 HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1006+65A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389210 | ||||||
chr5:69389240
|
T | G | 1 | a0001c0009t0001g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1006+95T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389240 | ||||||
chr5:69389457
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006+312C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389457 | ||||||
chr5:69389457
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1006+312C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389457 | ||||||
chr5:69389458
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006+313T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389458 | ||||||
chr5:69389528
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1006+383G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389528 | ||||||
chr5:69389580
|
C | CA | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1006+436dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69389580 | |||||
chr5:69389616
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1006+471G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389616 | ||||||
chr5:69389620
|
C | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0032others(121): Show | 126 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1006+475C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389620 | ||||||
chr5:69389683
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1006+538C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389683 | ||||||
chr5:69389798
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1006+653G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389798 | ||||||
chr5:69389858
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1006+713G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389858 | ||||||
chr5:69389858
|
G | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1006+713G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389858 | ||||||
chr5:69389887
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1006+742C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389887 | ||||||
chr5:69389957
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1006+812T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389957 | ||||||
chr5:69390398
|
G | A | 2 | a0001c0001t0003g0267a0001c0001t0003g0269 | 2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1006+1253G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390398 | ||||||
chr5:69390434
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1006+1289G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390434 | ||||||
chr5:69390695
|
C | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1007-1136C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390695 | ||||||
chr5:69390699
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1007-1132T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390699 | ||||||
chr5:69390797
|
AAT | A | 93 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1007-1020_1007-101 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390797 | |||||
chr5:69390838
|
C | T | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-993C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390838 | ||||||
chr5:69390916
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1007-915G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390916 | ||||||
chr5:69390952
|
C | CA | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1007-866dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | |||||
chr5:69390952
|
C | CAA | 10 | a0001c0001t0001g0232a0001c0007t0001g0241a0002c0002t0001g0196others(7): Show | 11 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-867_1007-866d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | |||||
chr5:69390952
|
CA | C | 95 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(92): Show | 95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1007-866delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | |||||
chr5:69390976
|
G | A | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1007-855G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390976 | ||||||
chr5:69391055
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007-776G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391055 | ||||||
chr5:69391094
|
C | T | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-737C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391094 | ||||||
chr5:69391120
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1007-711C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391120 | ||||||
chr5:69391122
|
C | T | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG01433.hp1 NA18949.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-709C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391122 | ||||||
chr5:69391229
|
CA | C | 96 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1007-584delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69391229 | |||||
chr5:69391687
|
A | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1007-144A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391687 | ||||||
chr5:69392199
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1189+186G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392199 | ||||||
chr5:69392358
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1189+345T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392358 | ||||||
chr5:69392582
|
G | T | 1 | a0002c0002t0001g0007 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1189+569G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392582 | ||||||
chr5:69392616
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1190-539A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392616 | ||||||
chr5:69392781
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1190-374T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392781 | ||||||
chr5:69393057
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1190-98G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69393057 | ||||||
chr5:69393710
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1422+210C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393710 | ||||||
chr5:69393908
|
G | GT | 7 | a0001c0001t0002g0277a0001c0001t0002g0280a0001c0001t0002g0283others(4): Show | 7 | HG01256.hp1 HG01256.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1422+431dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | |||||
chr5:69393908
|
G | GTT | 7 | a0001c0001t0001g0164a0001c0001t0001g0182a0002c0002t0001g0008others(4): Show | 8 | HG02258.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422+430_1422+431d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | |||||
chr5:69393908
|
G | GTTT | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(140): Show | 146 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1422+429_1422+431d others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | |||||
chr5:69393908
|
G | GTTTT | 16 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0188others(13): Show | 16 | HG00438.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1422+428_1422+431d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | |||||
chr5:69393908
|
G | T | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1422+408G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393908 | ||||||
chr5:69393908
|
GT | G | 89 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1422+431delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | |||||
chr5:69393945
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1422+445A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393945 | ||||||
chr5:69394059
|
T | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG00438.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1422+559T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394059 | ||||||
chr5:69394077
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1422+577C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394077 | ||||||
chr5:69394142
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1422+642C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394142 | ||||||
chr5:69394184
|
T | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1422+684T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394184 | ||||||
chr5:69394192
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1422+692C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394192 | ||||||
chr5:69394442
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1422+942T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394442 | ||||||
chr5:69394598
|
T | TTTAA | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1422+1099_1422+110 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69394598 | |||||
chr5:69394667
|
C | A | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1422+1167C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394667 | ||||||
chr5:69394782
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0141others(27): Show | 31 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.1422+1282C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394782 | ||||||
chr5:69395065
|
A | G | 7 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0079others(4): Show | 7 | NA18994.hp2 NA18995.hp2 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.1423-1332A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395065 | ||||||
chr5:69395111
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1423-1286C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395111 | ||||||
chr5:69395498
|
T | C | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1423-899T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395498 | ||||||
chr5:69395847
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1423-550G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395847 | ||||||
chr5:69395934
|
A | G | 6 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(3): Show | 7 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-463A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395934 | ||||||
chr5:69396091
|
C | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1423-306C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396091 | ||||||
chr5:69396217
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0255 | 3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1423-180A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396217 | ||||||
chr5:69396353
|
C | A | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1423-44C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396353 | ||||||
chr5:69396548
|
T | TA | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(252): Show | 260 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1572+19dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396548 | |||||
chr5:69396548
|
T | TAA | 93 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1572+18_1572+19dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396548 | |||||
chr5:69396645
|
GA | G | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+105delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396645 | |||||
chr5:69396707
|
A | T | 1 | a0002c0002t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+161A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396707 | ||||||
chr5:69396708
|
T | A | 1 | a0002c0002t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+162T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396708 | ||||||
chr5:69396709
|
A | T | 1 | a0002c0002t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+163A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396709 | ||||||
chr5:69396809
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1572+263C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396809 | ||||||
chr5:69396981
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1572+435A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396981 | ||||||
chr5:69397076
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1572+530C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397076 | ||||||
chr5:69397228
|
A | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1572+682A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397228 | ||||||
chr5:69397501
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1572+955C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397501 | ||||||
chr5:69397520
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1572+974G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397520 | ||||||
chr5:69397636
|
A | C | 2 | a0001c0001t0002g0311a0001c0001t0002g0347 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1572+1090A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397636 | ||||||
chr5:69397709
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1572+1163A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397709 | ||||||
chr5:69397737
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1572+1191G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397737 | ||||||
chr5:69397740
|
G | C | 7 | a0001c0001t0002g0288a0001c0001t0002g0318a0001c0001t0002g0332others(4): Show | 7 | HG02258.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+1194G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397740 | ||||||
chr5:69397784
|
T | G | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1572+1238T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397784 | ||||||
chr5:69397851
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1572+1305C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397851 | ||||||
chr5:69397855
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1572+1309C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397855 | ||||||
chr5:69398040
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1572+1494C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398040 | ||||||
chr5:69398073
|
C | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1572+1527C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398073 | ||||||
chr5:69398098
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1572+1552C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398098 | ||||||
chr5:69398115
|
T | TA | 12 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0207others(9): Show | 13 | HG00733.hp1 HG01074.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+1582dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398115 | |||||
chr5:69398144
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+1598G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398144 | ||||||
chr5:69398306
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1573-1743A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398306 | ||||||
chr5:69398314
|
A | G | 1 | a0001c0001t0002g0329 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1573-1735A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398314 | ||||||
chr5:69398342
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1573-1707A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398342 | ||||||
chr5:69398344
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(161): Show | 167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1573-1705A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398344 | ||||||
chr5:69398604
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1573-1445G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398604 | ||||||
chr5:69398707
|
G | A | 10 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0078others(7): Show | 10 | HG02129.hp2 HG03834.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-1342G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398707 | ||||||
chr5:69398723
|
G | A | 1 | a0001c0001t0002g0348 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1573-1326G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398723 | ||||||
chr5:69398811
|
GA | G | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00438.hp2 HG01167.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1573-1227delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398811 | |||||
chr5:69398868
|
T | TA | 87 | a0001c0001t0001g0032a0001c0001t0001g0178a0001c0001t0001g0193others(84): Show | 88 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(85): Show |
intron_variant | MODIFIER | c.1573-1161dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | |||||
chr5:69398868
|
T | TAA | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 153 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1573-1162_1573-116 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | |||||
chr5:69398868
|
T | TAAA | 18 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1573-1163_1573-116 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | |||||
chr5:69398868
|
T | TAAAA | 77 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(74): Show | 77 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1573-1164_1573-116 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | |||||
chr5:69398868
|
T | TAAAAA | 10 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(7): Show | 10 | HG00735.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-1165_1573-116 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | |||||
chr5:69399009
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1573-1040T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399009 | ||||||
chr5:69399018
|
A | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0125others(29): Show | 32 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1573-1031A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399018 | ||||||
chr5:69399282
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1573-767A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399282 | ||||||
chr5:69399347
|
A | G | 8 | a0001c0001t0001g0127a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG00558.hp1 NA18955.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-702A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399347 | ||||||
chr5:69399580
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0125others(28): Show | 31 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-469C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399580 | ||||||
chr5:69399685
|
C | CGTT | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1573-362_1573-361i others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69399685 | |||||
chr5:69400010
|
C | A | 1 | a0001c0001t0002g0347 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1573-39C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69400010 | ||||||
chr5:69400045
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18970.hp1 | splice_region_variant&intron_variant | LOW | c.1573-4A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69400045 | ||||||
chr5:69400208
|
G | GTTTATTT others(1): Show |
267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1693+55_1693+62dup others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | |||||
chr5:69400208
|
G | GTTTATTT others(5): Show |
1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1693+51_1693+62dup others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | |||||
chr5:69400208
|
G | GTTTATTT others(9): Show |
1 | a0003c0003t0001g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1693+47_1693+62dup others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | |||||
chr5:69400232
|
T | A | 1 | a0002c0002t0001g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1693+63T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400232 | ||||||
chr5:69400244
|
G | A | 6 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0299others(3): Show | 6 | HG02080.hp1 HG02155.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+75G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400244 | ||||||
chr5:69400273
|
G | A | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1693+104G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400273 | ||||||
chr5:69400280
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1693+111C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400280 | ||||||
chr5:69400467
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1693+298C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400467 | ||||||
chr5:69400510
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1693+341A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400510 | ||||||
chr5:69400579
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1693+410C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400579 | ||||||
chr5:69400596
|
T | A | 1 | a0002c0002t0001g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1693+427T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400596 | ||||||
chr5:69400626
|
G | GT | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1693+467dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400626 | |||||
chr5:69401023
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0032others(122): Show | 127 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1693+854A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401023 | ||||||
chr5:69401102
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1693+933C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401102 | ||||||
chr5:69401133
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1693+964C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401133 | ||||||
chr5:69401321
|
A | G | 1 | a0002c0002t0001g0012 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1693+1152A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401321 | ||||||
chr5:69401499
|
T | TA | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1693+1330_1693+133 others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401499 | ||||||
chr5:69401760
|
G | A | 8 | a0001c0001t0001g0131a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693+1591G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401760 | ||||||
chr5:69401783
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1693+1614C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401783 | ||||||
chr5:69401831
|
C | CA | 7 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0064others(4): Show | 7 | HG01192.hp1 HG01496.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+1670dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69401831 | |||||
chr5:69401839
|
A | C | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1693+1670A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401839 | ||||||
chr5:69401851
|
C | CA | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1693+1689dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69401851 | |||||
chr5:69402003
|
C | CA | 88 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(85): Show | 91 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1693+1858dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | |||||
chr5:69402003
|
C | CAA | 91 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0032others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1693+1857_1693+185 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | |||||
chr5:69402003
|
C | CAAA | 14 | a0001c0001t0001g0171a0001c0001t0001g0175a0001c0001t0001g0181others(11): Show | 14 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693+1856_1693+185 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | |||||
chr5:69402271
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1693+2102G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402271 | ||||||
chr5:69402273
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1693+2104A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402273 | ||||||
chr5:69402340
|
G | A | 2 | a0001c0001t0001g0232a0001c0007t0001g0241 | 2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1693+2171G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402340 | ||||||
chr5:69402341
|
C | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+2172C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402341 | ||||||
chr5:69402346
|
G | A | 1 | a0003c0003t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1693+2177G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402346 | ||||||
chr5:69402483
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0060 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1693+2314G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402483 | ||||||
chr5:69402654
|
C | CA | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1693+2500dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402654 | |||||
chr5:69402939
|
C | CA | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1693+2770_1693+277 others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402939 | ||||||
chr5:69403004
|
T | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1693+2835T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403004 | ||||||
chr5:69403019
|
A | G | 1 | a0001c0001t0002g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1693+2850A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403019 | ||||||
chr5:69403229
|
G | A | 1 | a0002c0002t0001g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1693+3060G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403229 | ||||||
chr5:69403568
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1693+3399A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403568 | ||||||
chr5:69403579
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1693+3410T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403579 | ||||||
chr5:69403621
|
T | C | 1 | a0002c0002t0001g0203 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1693+3452T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403621 | ||||||
chr5:69403682
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1693+3513G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403682 | ||||||
chr5:69403737
|
C | A | 1 | a0001c0001t0002g0345 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1693+3568C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403737 | ||||||
chr5:69403745
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1693+3576C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403745 | ||||||
chr5:69403937
|
AAAAAT | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+3779_1693+378 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69403937 | |||||
chr5:69403963
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1693+3794T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403963 | ||||||
chr5:69404011
|
ATTCTGTT | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+3852_1693+385 others(11): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404011 | |||||
chr5:69404399
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1693+4230A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404399 | ||||||
chr5:69404566
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02615.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1693+4397G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404566 | ||||||
chr5:69404625
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1693+4456T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404625 | ||||||
chr5:69404641
|
CG | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | NA18956.hp2 NA18989.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+4473delG | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404641 | ||||||
chr5:69404643
|
C | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | NA18956.hp2 NA18989.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+4474C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404643 | ||||||
chr5:69404769
|
C | CA | 10 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0078others(7): Show | 10 | HG00741.hp2 HG02071.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693+4614dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404769 | |||||
chr5:69404769
|
CA | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(164): Show | 171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1693+4614delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404769 | |||||
chr5:69404810
|
C | G | 1 | a0002c0002t0001g0216 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1693+4641C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404810 | ||||||
chr5:69404922
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1693+4753A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404922 | ||||||
chr5:69405043
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1693+4874C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405043 | ||||||
chr5:69405226
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1693+5057G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405226 | ||||||
chr5:69405256
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1693+5087C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405256 | ||||||
chr5:69405279
|
G | A | 9 | a0002c0002t0001g0023a0002c0002t0001g0136a0002c0002t0001g0151others(6): Show | 9 | HG02896.hp2 HG03453.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1693+5110G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405279 | ||||||
chr5:69405352
|
C | A | 1 | a0001c0001t0002g0314 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1694-5141C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405352 | ||||||
chr5:69405352
|
C | CA | 11 | a0001c0001t0001g0185a0001c0001t0001g0198a0001c0001t0001g0262others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-5129dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69405352 | |||||
chr5:69405354
|
A | C | 95 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(92): Show | 95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1694-5139A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405354 | ||||||
chr5:69405433
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1694-5060G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405433 | ||||||
chr5:69405503
|
C | A | 8 | a0001c0001t0001g0131a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694-4990C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405503 | ||||||
chr5:69405527
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1694-4966C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405527 | ||||||
chr5:69405551
|
C | T | 46 | a0001c0001t0002g0005a0001c0001t0002g0282a0001c0001t0002g0283others(43): Show | 47 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1694-4942C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405551 | ||||||
chr5:69405623
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-4870C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405623 | ||||||
chr5:69405677
|
CA | C | 49 | a0001c0001t0002g0005a0001c0001t0002g0276a0001c0001t0002g0277others(46): Show | 50 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694-4806delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69405677 | |||||
chr5:69405681
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0218 | 2 | HG02109.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1694-4812A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405681 | ||||||
chr5:69405806
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-4687C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405806 | ||||||
chr5:69405866
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1694-4627C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405866 | ||||||
chr5:69405913
|
A | T | 1 | a0001c0001t0002g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1694-4580A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405913 | ||||||
chr5:69405950
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1694-4543G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405950 | ||||||
chr5:69405974
|
A | G | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1694-4519A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405974 | ||||||
chr5:69406041
|
CA | C | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1694-4436delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406041 | |||||
chr5:69406300
|
A | G | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1694-4193A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406300 | ||||||
chr5:69406368
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1694-4125A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406368 | ||||||
chr5:69406461
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1694-4032A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406461 | ||||||
chr5:69406487
|
T | TTG | 36 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(33): Show | 36 | HG00423.hp2 HG00621.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.1694-3993_1694-399 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406487 | |||||
chr5:69406621
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1694-3872C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406621 | ||||||
chr5:69406747
|
T | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-3746T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406747 | ||||||
chr5:69406802
|
G | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1694-3691G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406802 | ||||||
chr5:69406999
|
A | AT | 7 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0275others(4): Show | 7 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-3473dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | |||||
chr5:69406999
|
AT | A | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1694-3473delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | |||||
chr5:69406999
|
ATT | A | 6 | a0001c0001t0001g0115a0003c0003t0001g0025a0003c0003t0001g0026others(3): Show | 6 | HG01256.hp1 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1694-3474_1694-347 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | |||||
chr5:69407362
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1694-3131G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407362 | ||||||
chr5:69407395
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-3098C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407395 | ||||||
chr5:69407562
|
G | GT | 6 | a0001c0001t0001g0240a0001c0001t0001g0275a0001c0001t0002g0348others(3): Show | 6 | HG00741.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1694-2900dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
G | GTT | 20 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(17): Show | 20 | HG00733.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1694-2901_1694-290 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
G | GTTT | 36 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0057others(33): Show | 36 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1694-2902_1694-290 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
G | GTTTT | 26 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1694-2903_1694-290 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
G | GTTTTT | 7 | a0001c0001t0001g0035a0001c0001t0001g0056a0001c0001t0001g0095others(4): Show | 7 | HG00621.hp1 HG01071.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-2904_1694-290 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GT | G | 93 | a0001c0001t0001g0219a0001c0001t0002g0005a0001c0001t0002g0272others(90): Show | 95 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.1694-2900delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GTT | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0166others(20): Show | 24 | HG00558.hp2 HG01074.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1694-2901_1694-290 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GTTT | G | 50 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0125others(47): Show | 51 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1694-2902_1694-290 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GTTTT | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0135a0001c0001t0001g0139others(23): Show | 27 | HG00438.hp1 HG01243.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1694-2903_1694-290 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0002g0353 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1694-2916_1694-290 others(21): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407562
|
GTTTTTTT others(11): Show |
G | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0303others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-2917_1694-290 others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | |||||
chr5:69407599
|
C | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0238 | 4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694-2894C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407599 | ||||||
chr5:69407737
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-2756C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407737 | ||||||
chr5:69407741
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-2752G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407741 | ||||||
chr5:69407809
|
C | T | 1 | a0002c0002t0001g0022 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1694-2684C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407809 | ||||||
chr5:69407827
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0218a0001c0001t0001g0220others(23): Show | 27 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.1694-2666C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407827 | ||||||
chr5:69407925
|
A | G | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1694-2568A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407925 | ||||||
chr5:69408119
|
C | T | 46 | a0001c0001t0002g0005a0001c0001t0002g0282a0001c0001t0002g0283others(43): Show | 47 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1694-2374C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408119 | ||||||
chr5:69408153
|
G | T | 1 | a0001c0001t0002g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1694-2340G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408153 | ||||||
chr5:69408179
|
T | C | 2 | a0001c0001t0002g0323a0001c0001t0002g0329 | 2 | NA18950.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1694-2314T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408179 | ||||||
chr5:69408191
|
ATTTTTTG others(30): Show |
A | 5 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0129others(2): Show | 5 | HG01071.hp2 HG01074.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2301_1694-226 others(41): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408191 | ||||||
chr5:69408274
|
TTTA | T | 3 | a0002c0002t0001g0154a0002c0002t0001g0155a0002c0002t0001g0268 | 3 | HG01081.hp1 HG01978.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1694-2216_1694-221 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408274 | |||||
chr5:69408376
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1694-2117C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408376 | ||||||
chr5:69408485
|
C | T | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-2008C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408485 | ||||||
chr5:69408506
|
C | CT | 20 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0105others(17): Show | 20 | HG00609.hp1 HG01243.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1694-1963dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | |||||
chr5:69408506
|
C | CTT | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 141 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1694-1964_1694-196 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | |||||
chr5:69408506
|
C | CTTT | 17 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0178others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1694-1965_1694-196 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | |||||
chr5:69408506
|
CT | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0064a0001c0001t0001g0090others(3): Show | 6 | HG01109.hp2 HG01168.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1694-1963delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | |||||
chr5:69408710
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0169 | 2 | HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1694-1783C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408710 | ||||||
chr5:69408754
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1694-1739A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408754 | ||||||
chr5:69408829
|
A | G | 7 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0025others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1694-1664A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408829 | ||||||
chr5:69408847
|
A | T | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-1646A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408847 | ||||||
chr5:69408885
|
G | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1694-1608G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408885 | ||||||
chr5:69409022
|
G | A | 9 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0323others(6): Show | 9 | HG04184.hp1 NA18950.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1694-1471G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409022 | ||||||
chr5:69409103
|
T | G | 2 | a0002c0002t0001g0136a0002c0002t0001g0151 | 2 | NA18970.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1694-1390T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409103 | ||||||
chr5:69409149
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1694-1344T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409149 | ||||||
chr5:69409321
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(345): Show | 353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.1694-1172A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409321 | ||||||
chr5:69409377
|
T | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1694-1116T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409377 | ||||||
chr5:69409553
|
T | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0071others(7): Show | 10 | HG02129.hp2 NA18959.hp1 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-940T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409553 | ||||||
chr5:69409573
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1694-920A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409573 | ||||||
chr5:69409583
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1694-910C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409583 | ||||||
chr5:69409603
|
A | T | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1694-890A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409603 | ||||||
chr5:69410349
|
A | G | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-144A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69410349 | ||||||
chr5:69410425
|
G | T | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1694-68G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69410425 | ||||||
chr5:69410574
|
A | G | 2 | a0001c0001t0001g0198a0001c0009t0001g0199 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1751+24A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410574 | ||||||
chr5:69410581
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1751+31T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410581 | ||||||
chr5:69410582
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+32G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410582 | ||||||
chr5:69410611
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1751+61G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410611 | ||||||
chr5:69410959
|
G | GTCTA | 14 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0132others(11): Show | 15 | HG00738.hp2 HG01258.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1751+412_1751+413i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410959 | |||||
chr5:69410963
|
G | A | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0032others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1751+413G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410963 | ||||||
chr5:69410965
|
C | CTA | 3 | a0001c0001t0001g0240a0001c0001t0002g0291a0001c0001t0002g0294 | 3 | HG03516.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1751+446_1751+447d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATA | 21 | a0001c0001t0002g0005a0001c0001t0002g0272a0001c0001t0002g0282others(18): Show | 22 | HG01081.hp2 HG01256.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1751+444_1751+447d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATA | 25 | a0001c0001t0001g0275a0001c0001t0002g0273a0001c0001t0002g0274others(22): Show | 25 | HG00642.hp1 HG00741.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1751+442_1751+447d others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATAT others(1): Show |
14 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1751+440_1751+447d others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATAT others(3): Show |
14 | a0001c0001t0002g0289a0001c0001t0002g0292a0001c0001t0002g0313others(11): Show | 14 | HG00609.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1751+438_1751+447d others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0002g0347 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1751+436_1751+447d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATAT others(7): Show |
5 | a0001c0001t0001g0219a0001c0001t0002g0287a0001c0001t0002g0299others(2): Show | 5 | HG02155.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751+434_1751+447d others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTATATAT others(9): Show |
3 | a0001c0001t0002g0311a0001c0001t0002g0328a0001c0001t0002g0336 | 3 | HG02647.hp1 HG03130.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1751+432_1751+447d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTG | 4 | a0002c0002t0001g0133a0003c0003t0001g0025a0003c0003t0001g0027others(1): Show | 4 | HG02004.hp1 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(1): Show |
9 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0094others(6): Show | 9 | HG00423.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(3): Show |
9 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0058others(6): Show | 9 | HG00733.hp2 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(5): Show |
30 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0052others(27): Show | 30 | HG00323.hp1 HG00642.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(7): Show |
21 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(18): Show | 21 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(9): Show |
16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0044others(13): Show | 16 | HG00735.hp1 HG02071.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(11): Show |
4 | a0001c0001t0001g0046a0001c0001t0001g0087a0001c0001t0001g0102others(1): Show | 4 | NA18944.hp2 NA18946.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(13): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0090 | 3 | NA18989.hp1 NA19054.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCCAT others(15): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0071 | 2 | NA18959.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTA | 46 | a0001c0001t0001g0004a0001c0001t0001g0125a0001c0001t0001g0126others(43): Show | 48 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(1): Show |
43 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0001g0197others(40): Show | 44 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(3): Show |
14 | a0001c0001t0001g0164a0001c0001t0001g0182a0001c0001t0001g0188others(11): Show | 14 | HG00558.hp2 HG00733.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(5): Show |
18 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0185others(15): Show | 18 | HG00423.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(7): Show |
16 | a0001c0001t0001g0032a0001c0001t0001g0074a0001c0001t0001g0131others(13): Show | 16 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(9): Show |
9 | a0001c0001t0001g0141a0001c0001t0001g0223a0001c0001t0001g0225others(6): Show | 9 | HG01109.hp1 HG03486.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(11): Show |
3 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0001t0001g0266 | 3 | NA18522.hp2 NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410965
|
C | CTGTCTAT others(13): Show |
4 | a0001c0001t0001g0194a0001c0001t0001g0230a0001c0001t0001g0265others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | |||||
chr5:69410966
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1751+416T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410966 | ||||||
chr5:69410967
|
A | C | 4 | a0002c0002t0001g0133a0003c0003t0001g0025a0003c0003t0001g0027others(1): Show | 4 | HG02004.hp1 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+417A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410967 | ||||||
chr5:69410967
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+417A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410967 | ||||||
chr5:69410969
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+419A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410969 | ||||||
chr5:69410971
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+421A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410971 | ||||||
chr5:69410973
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+423A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410973 | ||||||
chr5:69410975
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+425A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410975 | ||||||
chr5:69410998
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1751+448C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410998 | ||||||
chr5:69410998
|
C | T | 95 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(92): Show | 95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1751+448C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410998 | ||||||
chr5:69411262
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1751+712T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411262 | ||||||
chr5:69411267
|
T | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1751+717T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411267 | ||||||
chr5:69411270
|
G | T | 2 | a0002c0002t0001g0173a0002c0002t0001g0213 | 2 | HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1751+720G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411270 | ||||||
chr5:69411333
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0207others(6): Show | 10 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1751+783C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411333 | ||||||
chr5:69411336
|
A | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1751+786A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411336 | ||||||
chr5:69411474
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1751+924G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411474 | ||||||
chr5:69411545
|
T | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1751+995T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411545 | ||||||
chr5:69411605
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+1055G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411605 | ||||||
chr5:69411644
|
G | C | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1751+1094G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411644 | ||||||
chr5:69411690
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1751+1140A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411690 | ||||||
chr5:69411980
|
G | A | 1 | a0006c0013t0001g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1751+1430G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411980 | ||||||
chr5:69412039
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+1489C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412039 | ||||||
chr5:69412133
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+1583T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412133 | ||||||
chr5:69412181
|
C | T | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1751+1631C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412181 | ||||||
chr5:69412446
|
A | C | 1 | a0001c0001t0002g0312 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1752-1585A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412446 | ||||||
chr5:69412452
|
T | C | 4 | a0003c0003t0001g0025a0003c0003t0001g0026a0003c0003t0001g0027others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-1579T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412452 | ||||||
chr5:69412481
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1752-1550A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412481 | ||||||
chr5:69412496
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1752-1535T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412496 | ||||||
chr5:69412510
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1752-1521G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412510 | ||||||
chr5:69412659
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1752-1372C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412659 | ||||||
chr5:69412746
|
T | G | 2 | a0002c0002t0001g0145a0002c0002t0001g0196 | 2 | NA18948.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1752-1285T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412746 | ||||||
chr5:69412781
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1752-1250G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412781 | ||||||
chr5:69412784
|
T | C | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1752-1247T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412784 | ||||||
chr5:69412861
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1752-1170C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412861 | ||||||
chr5:69412984
|
CA | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1752-1034delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69412984 | |||||
chr5:69413196
|
T | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1752-835T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413196 | ||||||
chr5:69413421
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1752-610A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413421 | ||||||
chr5:69413597
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-434C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413597 | ||||||
chr5:69413682
|
G | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1752-349G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413682 | ||||||
chr5:69413823
|
T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1752-208T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413823 | ||||||
chr5:69413874
|
T | C | 1 | a0011c0012t0001g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1752-157T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413874 | ||||||
chr5:69413877
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1752-154T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413877 | ||||||
chr5:69414013
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1752-18G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69414013 |