geneid | 2547 |
---|---|
ensemblid | ENSG00000196419.13 |
hgncid | 4055 |
symbol | XRCC6 |
name | X-ray repair cross complementing 6 |
refseq_nuc | NM_001469.5 |
refseq_prot | NP_001460.1 |
ensembl_nuc | ENST00000360079.8 |
ensembl_prot | ENSP00000353192.3 |
mane_status | MANE Select |
chr | chr22 |
start | 41621295 |
end | 41664041 |
strand | + |
ver | v1.2 |
region | chr22:41621295-41664041 |
region5000 | chr22:41616295-41669041 |
regionname0 | XRCC6_chr22_41621295_41664041 |
regionname5000 | XRCC6_chr22_41616295_41669041 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 609 | 323 | 88 | 62 | 121 | 14 | 36 | 89 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0002 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1830 | 269 | 86 | 50 | 97 | 9 | 25 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
c0002 | 0/0 | 1830 | 54 | 2 | 12 | 24 | 5 | 11 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
c0003 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 293 | 312 | 88 | 59 | 113 | 14 | 36 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
t0002 | 0/0 | 293 | 9 | 0 | 0 | 9 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
t0003 | 0/0 | 293 | 3 | 0 | 3 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1830 | 269 | 86 | 50 | 97 | 9 | 25 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0001c0002 | 0/0 | 1830 | 54 | 2 | 12 | 24 | 5 | 11 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0002c0003 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2122 | 258 | 86 | 47 | 89 | 9 | 25 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0001c0001t0002 | 0/0 | 2122 | 8 | 0 | 0 | 8 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0001c0001t0003 | 0/0 | 2122 | 3 | 0 | 3 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0001c0002t0001 | 0/0 | 2122 | 54 | 2 | 12 | 24 | 5 | 11 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
a0002c0003t0002 | 0/0 | 2122 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | copy fasta | chr22 | 41616295 | 41669041 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0145 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0232 | EUR | IBS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | CDX | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0293 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19000 | hp2 | a0002 | c0003 | t0002 | g0057 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0289 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0246 | REF | REF | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0092 | REF | REF | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41636606
|
C | T | 1 | a0002 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.425C>T | p.Ser142Leu | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/13 | 491/2122 | 425/1830 | 142/609 | chr22 | 41636606 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41663764
|
G | T | 1 | a0001c0002 | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
synonymous_variant | LOW | c.1779G>T | p.Gly593Gly | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 13/13 | 1845/2122 | 1779/1830 | 593/609 | chr22 | 41663764 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41663824
|
C | T | 1 | a0001c0001t0003 | 3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 13/13 | 9 | chr22 | 41663824 | |||||
chr22:41663850
|
G | T | 2 | a0001c0001t0002a0002c0003t0002 | 9 | HG02071.hp2 NA18969.hp1 NA18975.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 13/13 | 35 | chr22 | 41663850 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41621350
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-16+5G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621350 | ||||||
chr22:41621456
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-16+111G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621456 | ||||||
chr22:41621502
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-16+157G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621502 | ||||||
chr22:41621531
|
CGCGTTTG others(10): Show |
C | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+207_-16+223del others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 41621531 | |||||
chr22:41621544
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-16+199C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621544 | ||||||
chr22:41621625
|
T | C | 3 | a0001c0001t0001g0022a0001c0002t0001g0020a0001c0002t0001g0021 | 3 | HG02602.hp2 HG02630.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-16+280T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621625 | ||||||
chr22:41621649
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+304G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621649 | ||||||
chr22:41621662
|
A | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+317A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621662 | ||||||
chr22:41621769
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-15-221G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621769 | ||||||
chr22:41621844
|
A | G | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-146A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 1/12 | chr22 | 41621844 | ||||||
chr22:41622277
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+191C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622277 | ||||||
chr22:41622279
|
A | G | 1 | a0001c0002t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.82+193A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622279 | ||||||
chr22:41622428
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82+342A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622428 | ||||||
chr22:41622497
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.82+411T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622497 | ||||||
chr22:41622683
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.82+597G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622683 | ||||||
chr22:41622705
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.82+619C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622705 | ||||||
chr22:41622945
|
G | GA | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+871dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41622945 | |||||
chr22:41622997
|
T | G | 1 | a0001c0001t0001g0031 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.82+911T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41622997 | ||||||
chr22:41623026
|
C | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+940C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623026 | ||||||
chr22:41623033
|
T | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.82+947T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623033 | ||||||
chr22:41623217
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82+1131A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623217 | ||||||
chr22:41623247
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.82+1161C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623247 | ||||||
chr22:41623374
|
C | T | 2 | a0001c0002t0001g0288a0001c0002t0001g0289 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.82+1288C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623374 | ||||||
chr22:41623377
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1291A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623377 | ||||||
chr22:41623450
|
C | T | 6 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 6 | NA18962.hp1 NA18966.hp1 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1364C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623450 | ||||||
chr22:41623480
|
C | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.82+1394C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623480 | ||||||
chr22:41623482
|
G | A | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1396G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623482 | ||||||
chr22:41623491
|
C | G | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+1405C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623491 | ||||||
chr22:41623577
|
C | T | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+1491C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623577 | ||||||
chr22:41623631
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.82+1545C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623631 | ||||||
chr22:41623634
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.82+1548T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623634 | ||||||
chr22:41623737
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.82+1651T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623737 | ||||||
chr22:41623832
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0002t0001g0275 | 3 | HG00597.hp1 HG02083.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.82+1746C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623832 | ||||||
chr22:41623871
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.82+1785C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623871 | ||||||
chr22:41623884
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024 | 4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1798G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623884 | ||||||
chr22:41623975
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.82+1889G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41623975 | ||||||
chr22:41624041
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.82+1955T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624041 | ||||||
chr22:41624069
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1983C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624069 | ||||||
chr22:41624231
|
C | G | 1 | a0001c0001t0001g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.82+2145C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624231 | ||||||
chr22:41624236
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.82+2150G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624236 | ||||||
chr22:41624309
|
A | AC | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2225dupC | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41624309 | |||||
chr22:41624383
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.82+2297A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624383 | ||||||
chr22:41624409
|
G | A | 5 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+2323G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624409 | ||||||
chr22:41624511
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.82+2425C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624511 | ||||||
chr22:41624636
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(310): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.82+2550T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624636 | ||||||
chr22:41624719
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.82+2633C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624719 | ||||||
chr22:41624723
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.82+2637C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624723 | ||||||
chr22:41624878
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.82+2792T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624878 | ||||||
chr22:41624983
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 19 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+2897C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624983 | ||||||
chr22:41625046
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2960C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625046 | ||||||
chr22:41625124
|
G | C | 7 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0001g0310others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-2994G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625124 | ||||||
chr22:41625206
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.83-2912A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625206 | ||||||
chr22:41625208
|
GCGGGAGA others(12): Show |
G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.83-2903_83-2885del others(19): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41625208 | |||||
chr22:41625218
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 19 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-2900C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625218 | ||||||
chr22:41625269
|
A | G | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2849A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625269 | ||||||
chr22:41625368
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2750G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625368 | ||||||
chr22:41625420
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.83-2698C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625420 | ||||||
chr22:41625676
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.83-2442A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625676 | ||||||
chr22:41625679
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.83-2439G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625679 | ||||||
chr22:41625953
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.83-2165C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41625953 | ||||||
chr22:41626012
|
G | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0272 | 2 | NA18906.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.83-2106G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626012 | ||||||
chr22:41626031
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.83-2087C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626031 | ||||||
chr22:41626173
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0268a0001c0001t0001g0269 | 4 | HG01934.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-1945C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626173 | ||||||
chr22:41626393
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.83-1725G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626393 | ||||||
chr22:41626631
|
G | GT | 16 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG00423.hp1 HG00621.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-1476dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41626631 | |||||
chr22:41626632
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.83-1486T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626632 | ||||||
chr22:41626635
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.83-1483T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626635 | ||||||
chr22:41626642
|
TG | T | 5 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG02300.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-1475delG | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626642 | ||||||
chr22:41626643
|
G | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.83-1475G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626643 | ||||||
chr22:41626662
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0204 | 3 | HG00673.hp1 NA18971.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.83-1456G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626662 | ||||||
chr22:41626752
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83-1366C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626752 | ||||||
chr22:41626782
|
T | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.83-1336T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626782 | ||||||
chr22:41626784
|
T | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | NA18961.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.83-1334T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626784 | ||||||
chr22:41626833
|
G | T | 1 | a0001c0002t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.83-1285G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41626833 | ||||||
chr22:41627338
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-780C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627338 | ||||||
chr22:41627450
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.83-668A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627450 | ||||||
chr22:41627547
|
G | T | 8 | a0001c0001t0001g0028a0001c0001t0001g0197a0001c0002t0001g0196others(5): Show | 8 | HG00408.hp1 HG00544.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-571G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627547 | ||||||
chr22:41627583
|
C | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0036 | 3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.83-535C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627583 | ||||||
chr22:41627609
|
C | CA | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.83-488dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41627609 | |||||
chr22:41627609
|
C | CAA | 23 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0115others(20): Show | 24 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.83-489_83-488dupAA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41627609 | |||||
chr22:41627609
|
C | CAAAA | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-491_83-488dupAA others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41627609 | |||||
chr22:41627609
|
CAAAA | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.83-491_83-488delAA others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41627609 | |||||
chr22:41627710
|
A | G | 13 | a0001c0001t0001g0049a0001c0001t0001g0080a0001c0001t0001g0081others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.83-408A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627710 | ||||||
chr22:41627921
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83-197T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627921 | ||||||
chr22:41627936
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(50): Show | 58 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.83-182G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627936 | ||||||
chr22:41627983
|
A | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.83-135A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627983 | ||||||
chr22:41627993
|
T | G | 1 | a0001c0002t0001g0201 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.83-125T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41627993 | ||||||
chr22:41628102
|
A | AT | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.83-9dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 41628102 | |||||
chr22:41628316
|
T | G | 1 | a0001c0002t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.195+86T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41628316 | ||||||
chr22:41628324
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+94C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41628324 | ||||||
chr22:41628561
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+331A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41628561 | ||||||
chr22:41628633
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(5): Show | 9 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+403A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41628633 | ||||||
chr22:41628654
|
T | C | 7 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0001g0310others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+424T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41628654 | ||||||
chr22:41628965
|
C | CA | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.195+759dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41628965 | |||||
chr22:41628965
|
C | CAA | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0028others(55): Show | 59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.195+758_195+759dup others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41628965 | |||||
chr22:41628965
|
CA | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 21 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+759delA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41628965 | |||||
chr22:41629053
|
A | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 43 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.195+823A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629053 | ||||||
chr22:41629215
|
G | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 43 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.195+985G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629215 | ||||||
chr22:41629276
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.195+1046C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629276 | ||||||
chr22:41629324
|
T | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02723.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.195+1094T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629324 | ||||||
chr22:41629346
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.195+1116A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629346 | ||||||
chr22:41629573
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+1343A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629573 | ||||||
chr22:41629652
|
G | GTATT | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+1440_195+1443d others(6): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41629652 | |||||
chr22:41629676
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.195+1446A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629676 | ||||||
chr22:41629722
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 19 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+1492T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629722 | ||||||
chr22:41629819
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0001g0106others(11): Show | 14 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.195+1589G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629819 | ||||||
chr22:41629841
|
T | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+1611T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629841 | ||||||
chr22:41629861
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+1631G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629861 | ||||||
chr22:41629917
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0254a0001c0001t0001g0262 | 3 | HG02145.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.195+1687C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629917 | ||||||
chr22:41629983
|
C | CT | 24 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0059others(21): Show | 24 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.195+1772dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41629983 | |||||
chr22:41629983
|
CTT | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(47): Show | 55 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+1771_195+1772d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41629983 | |||||
chr22:41629984
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.195+1754T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629984 | ||||||
chr22:41629986
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.195+1756T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41629986 | ||||||
chr22:41630045
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.195+1815A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630045 | ||||||
chr22:41630489
|
C | CT | 203 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.195+2274dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41630489 | |||||
chr22:41630489
|
C | CTT | 19 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 21 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+2273_195+2274d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41630489 | |||||
chr22:41630551
|
G | T | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+2321G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630551 | ||||||
chr22:41630552
|
G | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2322G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630552 | ||||||
chr22:41630590
|
C | T | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG02257.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.195+2360C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630590 | ||||||
chr22:41630618
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+2388C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630618 | ||||||
chr22:41630727
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+2497A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630727 | ||||||
chr22:41630775
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(50): Show | 58 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.195+2545T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630775 | ||||||
chr22:41630808
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.195+2578G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630808 | ||||||
chr22:41630852
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.195+2622A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630852 | ||||||
chr22:41630889
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.195+2659G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630889 | ||||||
chr22:41630900
|
C | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+2670C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630900 | ||||||
chr22:41630987
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.195+2757C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41630987 | ||||||
chr22:41630991
|
C | CG | 5 | a0001c0001t0001g0114a0001c0001t0001g0181a0001c0001t0001g0219others(2): Show | 5 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2765dupG | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41630991 | |||||
chr22:41631064
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+2834C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631064 | ||||||
chr22:41631081
|
C | T | 1 | a0001c0002t0001g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.195+2851C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631081 | ||||||
chr22:41631083
|
GGT | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.195+2855_195+2856d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41631083 | |||||
chr22:41631092
|
A | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.195+2862A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631092 | ||||||
chr22:41631092
|
ATGACCCC others(42): Show |
A | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.195+2883_195+2931d others(51): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41631092 | |||||
chr22:41631110
|
T | G | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+2880T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631110 | ||||||
chr22:41631123
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.195+2893G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631123 | ||||||
chr22:41631135
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027 | 5 | HG02965.hp2 HG03130.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2905G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631135 | ||||||
chr22:41631140
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.195+2910G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631140 | ||||||
chr22:41631230
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.195+3000C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631230 | ||||||
chr22:41631331
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(50): Show | 58 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.195+3101T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631331 | ||||||
chr22:41631335
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195+3105G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631335 | ||||||
chr22:41631371
|
C | T | 3 | a0001c0001t0001g0157a0001c0002t0001g0113a0001c0002t0001g0156 | 3 | HG01069.hp2 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.195+3141C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631371 | ||||||
chr22:41631408
|
C | T | 2 | a0001c0001t0001g0157a0001c0002t0001g0156 | 2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.195+3178C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631408 | ||||||
chr22:41631411
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+3181C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631411 | ||||||
chr22:41631500
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.195+3270T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631500 | ||||||
chr22:41631533
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.195+3303C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631533 | ||||||
chr22:41631547
|
C | T | 1 | a0001c0002t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.195+3317C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631547 | ||||||
chr22:41631585
|
A | ACGCTCCT others(33): Show |
258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.195+3389_195+3390i others(42): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41631585 | |||||
chr22:41631625
|
A | G | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+3395A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631625 | ||||||
chr22:41631636
|
T | G | 5 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+3406T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631636 | ||||||
chr22:41631720
|
C | CG | 11 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0114others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+3494dupG | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41631720 | |||||
chr22:41631721
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.195+3491G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631721 | ||||||
chr22:41631732
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+3502C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631732 | ||||||
chr22:41631733
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.195+3503G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631733 | ||||||
chr22:41631740
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+3510G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631740 | ||||||
chr22:41631782
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+3552G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631782 | ||||||
chr22:41631819
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.195+3589G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631819 | ||||||
chr22:41631875
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+3645C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631875 | ||||||
chr22:41631911
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.195+3681C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631911 | ||||||
chr22:41631940
|
A | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | NA18961.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.195+3710A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631940 | ||||||
chr22:41631947
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.195+3717G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631947 | ||||||
chr22:41631988
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.195+3758C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41631988 | ||||||
chr22:41632016
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+3786T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632016 | ||||||
chr22:41632017
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+3787G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632017 | ||||||
chr22:41632104
|
A | G | 7 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0160others(4): Show | 7 | HG00609.hp2 NA18950.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+3874A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632104 | ||||||
chr22:41632121
|
A | G | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.195+3891A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632121 | ||||||
chr22:41632125
|
A | AGGGAGAG others(10): Show |
21 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+3923_195+3939d others(19): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41632125 | |||||
chr22:41632125
|
AGGGAGAG others(10): Show |
A | 8 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 10 | HG02129.hp1 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+3923_195+3939d others(19): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41632125 | |||||
chr22:41632157
|
G | A | 7 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0001g0310others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+3927G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632157 | ||||||
chr22:41632170
|
T | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 19 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+3940T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632170 | ||||||
chr22:41632401
|
A | T | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.196-3712A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632401 | ||||||
chr22:41632456
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.196-3657C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632456 | ||||||
chr22:41632538
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0040 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.196-3575G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632538 | ||||||
chr22:41632734
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.196-3379G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41632734 | ||||||
chr22:41632824
|
T | TG | 5 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0189others(2): Show | 6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-3287dupG | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41632824 | |||||
chr22:41632826
|
G | GA | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0184others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-3272dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41632826 | |||||
chr22:41633103
|
G | A | 1 | a0001c0002t0001g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.196-3010G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633103 | ||||||
chr22:41633216
|
C | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.196-2897C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633216 | ||||||
chr22:41633377
|
C | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-2736C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633377 | ||||||
chr22:41633397
|
A | AT | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG00544.hp1 HG00741.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-2701dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41633397 | |||||
chr22:41633434
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.196-2679G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633434 | ||||||
chr22:41633579
|
C | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-2534C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633579 | ||||||
chr22:41633617
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196-2496G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633617 | ||||||
chr22:41633661
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.196-2452A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633661 | ||||||
chr22:41633771
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196-2342G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41633771 | ||||||
chr22:41634068
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-2045C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634068 | ||||||
chr22:41634138
|
G | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG04184.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.196-1975G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634138 | ||||||
chr22:41634171
|
A | G | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1942A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634171 | ||||||
chr22:41634186
|
A | AT | 9 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0099others(6): Show | 9 | HG02257.hp1 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1910dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41634186 | |||||
chr22:41634186
|
AT | A | 9 | a0001c0001t0001g0082a0001c0001t0001g0195a0001c0001t0001g0212others(6): Show | 9 | HG00323.hp1 HG01099.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1910delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41634186 | |||||
chr22:41634201
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.196-1912T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634201 | ||||||
chr22:41634254
|
C | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-1859C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634254 | ||||||
chr22:41634287
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.196-1826G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634287 | ||||||
chr22:41634325
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-1788G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634325 | ||||||
chr22:41634355
|
T | C | 1 | a0001c0002t0001g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196-1758T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634355 | ||||||
chr22:41634486
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-1627C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634486 | ||||||
chr22:41634531
|
G | A | 1 | a0001c0002t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.196-1582G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634531 | ||||||
chr22:41634546
|
CT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.196-1551delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41634546 | |||||
chr22:41634546
|
CTT | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 7 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-1552_196-1551d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41634546 | |||||
chr22:41634575
|
C | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 19 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-1538C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634575 | ||||||
chr22:41634605
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-1508C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634605 | ||||||
chr22:41634667
|
C | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-1446C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634667 | ||||||
chr22:41634771
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-1342C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41634771 | ||||||
chr22:41635081
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.196-1032C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635081 | ||||||
chr22:41635086
|
A | T | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1027A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635086 | ||||||
chr22:41635098
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.196-1015G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635098 | ||||||
chr22:41635130
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.196-983T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635130 | ||||||
chr22:41635285
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.196-828C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635285 | ||||||
chr22:41635423
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196-690A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635423 | ||||||
chr22:41635486
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-627T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635486 | ||||||
chr22:41635708
|
G | GT | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.196-396dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41635708 | |||||
chr22:41635712
|
T | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-401T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635712 | ||||||
chr22:41635747
|
G | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.196-366G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635747 | ||||||
chr22:41635764
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.196-349T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635764 | ||||||
chr22:41635803
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-310A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635803 | ||||||
chr22:41635826
|
T | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-287T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635826 | ||||||
chr22:41635849
|
T | A | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.196-264T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635849 | ||||||
chr22:41635949
|
C | G | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.196-164C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635949 | ||||||
chr22:41636099
|
A | AT | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.196-4dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 41636099 | |||||
chr22:41636358
|
TG | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.334+108delG | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 4/12 | chr22 | 41636358 | ||||||
chr22:41636477
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.335-39C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 4/12 | chr22 | 41636477 | ||||||
chr22:41636811
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.589+41A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41636811 | ||||||
chr22:41636873
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.589+103A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41636873 | ||||||
chr22:41637077
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.589+307G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41637077 | ||||||
chr22:41637078
|
A | AT | 12 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0075others(9): Show | 12 | HG00741.hp1 HG01175.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+331dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 41637078 | |||||
chr22:41637078
|
AT | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.589+331delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 41637078 | |||||
chr22:41637078
|
ATT | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0040others(9): Show | 12 | HG00408.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+330_589+331del others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 41637078 | |||||
chr22:41637186
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.589+416C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41637186 | ||||||
chr22:41637286
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.590-322C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41637286 | ||||||
chr22:41637494
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.590-114A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 5/12 | chr22 | 41637494 | ||||||
chr22:41637961
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.773+170C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41637961 | ||||||
chr22:41637962
|
T | TA | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.773+190dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41637962 | |||||
chr22:41637962
|
T | TAA | 76 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0028others(73): Show | 78 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.773+189_773+190dup others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41637962 | |||||
chr22:41638244
|
CAT | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(8): Show | 12 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+454_773+455del others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638244 | ||||||
chr22:41638429
|
G | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.773+638G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638429 | ||||||
chr22:41638501
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.773+710T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638501 | ||||||
chr22:41638551
|
C | T | 1 | a0001c0002t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.773+760C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638551 | ||||||
chr22:41638675
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.773+884C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638675 | ||||||
chr22:41638705
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.773+914G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638705 | ||||||
chr22:41638755
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.773+964T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638755 | ||||||
chr22:41638771
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.773+980C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638771 | ||||||
chr22:41638772
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+981G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638772 | ||||||
chr22:41638776
|
C | CA | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(106): Show | 113 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.773+1007dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41638776 | |||||
chr22:41638776
|
C | CAA | 6 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0189others(3): Show | 7 | HG00438.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+1006_773+1007d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41638776 | |||||
chr22:41638776
|
C | CAAA | 9 | a0001c0001t0001g0024a0001c0001t0001g0271a0001c0001t0001g0298others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.773+1005_773+1007d others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41638776 | |||||
chr22:41638776
|
C | CAAAA | 9 | a0001c0001t0001g0009a0001c0001t0001g0299a0001c0001t0001g0300others(6): Show | 10 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.773+1004_773+1007d others(6): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41638776 | |||||
chr22:41638804
|
A | G | 1 | a0001c0002t0001g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.773+1013A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638804 | ||||||
chr22:41638848
|
G | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(8): Show | 12 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+1057G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638848 | ||||||
chr22:41638860
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.773+1069C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638860 | ||||||
chr22:41638893
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.773+1102T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41638893 | ||||||
chr22:41639158
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.773+1367C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41639158 | ||||||
chr22:41639329
|
C | CT | 29 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0045others(26): Show | 29 | HG00621.hp2 HG00639.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.773+1563dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTT | 6 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+1562_773+1563d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTT | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0016others(60): Show | 65 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.773+1559_773+1563d others(7): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTTT | 74 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0028others(71): Show | 76 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.773+1558_773+1563d others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTTTT | 37 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 38 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.773+1557_773+1563d others(9): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTTTT others(1): Show |
15 | a0001c0001t0001g0114a0001c0001t0001g0162a0001c0001t0001g0172others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.773+1556_773+1563d others(10): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02559.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.773+1554_773+1563d others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.773+1553_773+1563d others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
CT | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(2): Show | 7 | HG01070.hp1 HG02258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+1563delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
CTTTTT | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0035others(8): Show | 11 | HG01943.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.773+1559_773+1563d others(7): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
CTTTTTT | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 20 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.773+1558_773+1563d others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.773+1551_773+1563d others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639329
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.773+1548_773+1563d others(18): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639329 | |||||
chr22:41639480
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.773+1689T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41639480 | ||||||
chr22:41639667
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.773+1880_773+1889d others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639667 | |||||
chr22:41639667
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0220a0001c0001t0001g0235others(1): Show | 4 | HG02896.hp1 HG03704.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+1879_773+1889d others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639667 | |||||
chr22:41639667
|
C | CTTTTTTT others(5): Show |
226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(223): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.773+1878_773+1889d others(14): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639667 | |||||
chr22:41639667
|
C | CTTTTTTT others(6): Show |
21 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(18): Show | 21 | HG00280.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.773+1877_773+1889d others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639667 | |||||
chr22:41639667
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.773+1889_773+1890i others(16): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639667 | |||||
chr22:41639691
|
C | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.773+1900C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41639691 | ||||||
chr22:41639771
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.773+1980T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41639771 | ||||||
chr22:41639900
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.773+2109C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41639900 | ||||||
chr22:41639966
|
G | GT | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.773+2183dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41639966 | |||||
chr22:41640013
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.773+2222G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640013 | ||||||
chr22:41640083
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.773+2292A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640083 | ||||||
chr22:41640086
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.773+2295A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640086 | ||||||
chr22:41640305
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.773+2514C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640305 | ||||||
chr22:41640370
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.773+2579T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640370 | ||||||
chr22:41640428
|
C | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+2637C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640428 | ||||||
chr22:41640492
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.773+2701C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640492 | ||||||
chr22:41640504
|
G | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(50): Show | 58 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.773+2713G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640504 | ||||||
chr22:41640698
|
T | A | 7 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0001g0310others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+2907T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640698 | ||||||
chr22:41640908
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0014 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.773+3117G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640908 | ||||||
chr22:41640966
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.773+3175G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41640966 | ||||||
chr22:41641167
|
AATT | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+3380_773+3382d others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41641167 | |||||
chr22:41641305
|
AC | A | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.773+3515delC | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641305 | ||||||
chr22:41641342
|
G | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.773+3551G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641342 | ||||||
chr22:41641356
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(309): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.773+3565C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641356 | ||||||
chr22:41641608
|
C | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.773+3817C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641608 | ||||||
chr22:41641664
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.773+3873C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641664 | ||||||
chr22:41641799
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.773+4008C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641799 | ||||||
chr22:41641828
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.773+4037T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641828 | ||||||
chr22:41641897
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.773+4106G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641897 | ||||||
chr22:41641986
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.773+4195A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641986 | ||||||
chr22:41642220
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.773+4429A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642220 | ||||||
chr22:41642253
|
C | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.773+4462C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642253 | ||||||
chr22:41642355
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.774-4541A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642355 | ||||||
chr22:41642436
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0247 | 2 | NA18953.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.774-4460G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642436 | ||||||
chr22:41642451
|
C | G | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG02257.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.774-4445C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642451 | ||||||
chr22:41642636
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.774-4260A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642636 | ||||||
chr22:41642782
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.774-4114C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642782 | ||||||
chr22:41642787
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.774-4109A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642787 | ||||||
chr22:41642887
|
G | C | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.774-4009G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642887 | ||||||
chr22:41642902
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.774-3994T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41642902 | ||||||
chr22:41643477
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.774-3419G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643477 | ||||||
chr22:41643505
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0221a0001c0001t0001g0239 | 3 | HG01517.hp2 HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.774-3391C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643505 | ||||||
chr22:41643531
|
A | C | 1 | a0001c0001t0001g0030 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.774-3365A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643531 | ||||||
chr22:41643546
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.774-3350C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643546 | ||||||
chr22:41643677
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(51): Show | 59 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.774-3219T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643677 | ||||||
chr22:41643682
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0189others(2): Show | 6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-3214G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643682 | ||||||
chr22:41643782
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0038 | 3 | HG00408.hp2 HG00423.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.774-3114C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643782 | ||||||
chr22:41643820
|
C | CA | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(25): Show | 32 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.774-3061dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41643820 | |||||
chr22:41643984
|
C | CA | 20 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0298others(17): Show | 21 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.774-2899dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41643984 | |||||
chr22:41643984
|
C | CAA | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-2900_774-2899d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41643984 | |||||
chr22:41643999
|
T | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0182others(4): Show | 8 | NA18943.hp1 NA18951.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.774-2897T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41643999 | ||||||
chr22:41644099
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-2797A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644099 | ||||||
chr22:41644373
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(23): Show | 30 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.774-2523A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644373 | ||||||
chr22:41644394
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.774-2502A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644394 | ||||||
chr22:41644414
|
CT | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.774-2475delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41644414 | |||||
chr22:41644628
|
G | T | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.774-2268G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644628 | ||||||
chr22:41644669
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.774-2227A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644669 | ||||||
chr22:41644673
|
G | A | 5 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.774-2223G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41644673 | ||||||
chr22:41645026
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-1870G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645026 | ||||||
chr22:41645072
|
G | A | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-1824G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645072 | ||||||
chr22:41645300
|
T | TA | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(3): Show | 6 | HG00741.hp2 HG01243.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-1584dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645300 | |||||
chr22:41645306
|
A | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0046others(76): Show | 81 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.774-1590A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645306 | ||||||
chr22:41645321
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.774-1575A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645321 | ||||||
chr22:41645387
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.774-1509A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645387 | ||||||
chr22:41645391
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-1505A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645391 | ||||||
chr22:41645490
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0023 | 3 | HG01109.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.774-1406C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645490 | ||||||
chr22:41645510
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.774-1386G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645510 | ||||||
chr22:41645563
|
CACAGCAA others(4): Show |
C | 1 | a0001c0001t0001g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.774-1331_774-1321d others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645563 | |||||
chr22:41645576
|
G | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.774-1320G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645576 | ||||||
chr22:41645599
|
CTG | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.774-1295_774-1294d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645599 | |||||
chr22:41645615
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(22): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.774-1281G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645615 | ||||||
chr22:41645643
|
TTTTTG | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.774-1240_774-1236d others(7): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645643 | |||||
chr22:41645698
|
C | CT | 14 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 16 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-1182dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645698 | |||||
chr22:41645698
|
C | CTT | 6 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0001g0294others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-1183_774-1182d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 41645698 | |||||
chr22:41645820
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.774-1076C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645820 | ||||||
chr22:41645849
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-1047C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645849 | ||||||
chr22:41645966
|
T | A | 1 | a0001c0001t0001g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.774-930T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41645966 | ||||||
chr22:41646036
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-860G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646036 | ||||||
chr22:41646043
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.774-853C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646043 | ||||||
chr22:41646094
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-802G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646094 | ||||||
chr22:41646158
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.774-738C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646158 | ||||||
chr22:41646394
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.774-502A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646394 | ||||||
chr22:41646489
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.774-407C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646489 | ||||||
chr22:41646654
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.774-242A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646654 | ||||||
chr22:41646799
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.774-97G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646799 | ||||||
chr22:41646878
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.774-18C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41646878 | ||||||
chr22:41647092
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.960+10G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647092 | ||||||
chr22:41647138
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.960+56G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647138 | ||||||
chr22:41647359
|
G | T | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.960+277G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647359 | ||||||
chr22:41647376
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.960+294G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647376 | ||||||
chr22:41647442
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024 | 4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+360A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647442 | ||||||
chr22:41647465
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+383C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647465 | ||||||
chr22:41647581
|
C | CA | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.960+515dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41647581 | |||||
chr22:41647581
|
CA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+515delA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41647581 | |||||
chr22:41647935
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.960+853C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647935 | ||||||
chr22:41647966
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.960+884G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647966 | ||||||
chr22:41647967
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.960+885C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41647967 | ||||||
chr22:41648019
|
T | TCCCTC | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.960+974_960+978dup others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
T | TCCCTCCC others(3): Show |
41 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(38): Show | 42 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.960+969_960+978dup others(10): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
T | TCCCTCCC others(8): Show |
8 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 8 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+964_960+978dup others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
T | TCCCTCCC others(13): Show |
1 | a0001c0001t0001g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.960+959_960+978dup others(20): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
T | TCCCTCCC others(18): Show |
1 | a0001c0001t0001g0166 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.960+954_960+978dup others(25): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
TCCCTC | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG01099.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.960+974_960+978del others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
TCCCTCCC others(3): Show |
T | 2 | a0001c0001t0001g0233a0001c0001t0001g0272 | 2 | HG00099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.960+969_960+978del others(10): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648019
|
TCCCTCCC others(8): Show |
T | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(44): Show | 52 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.960+964_960+978del others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648019 | |||||
chr22:41648049
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.960+967C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648049 | ||||||
chr22:41648058
|
T | TCCCCTCC others(4): Show |
1 | a0001c0001t0001g0171 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.960+978_960+979ins others(11): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648058 | |||||
chr22:41648093
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.960+1011C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648093 | ||||||
chr22:41648175
|
C | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+1093C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648175 | ||||||
chr22:41648200
|
T | A | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1118T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648200 | ||||||
chr22:41648236
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0023 | 3 | HG01109.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.960+1154C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648236 | ||||||
chr22:41648310
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1228A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648310 | ||||||
chr22:41648349
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+1267G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648349 | ||||||
chr22:41648455
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+1373A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648455 | ||||||
chr22:41648694
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0037 | 3 | NA18994.hp2 NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.960+1612C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648694 | ||||||
chr22:41648696
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.960+1614A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648696 | ||||||
chr22:41648714
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.960+1632T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648714 | ||||||
chr22:41648795
|
T | TAACTAAT others(36): Show |
1 | a0001c0001t0002g0067 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.960+1714_960+1756d others(45): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41648795 | |||||
chr22:41648825
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.960+1743G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648825 | ||||||
chr22:41648892
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1810C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41648892 | ||||||
chr22:41649001
|
G | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0246 | 2 | NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.961-1722G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649001 | ||||||
chr22:41649005
|
A | AAAC | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.961-1717_961-1716i others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649005 | |||||
chr22:41649049
|
T | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(8): Show | 12 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.961-1674T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649049 | ||||||
chr22:41649050
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.961-1673C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649050 | ||||||
chr22:41649053
|
A | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0144a0001c0001t0001g0268others(1): Show | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-1670A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649053 | ||||||
chr22:41649095
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-1628C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649095 | ||||||
chr22:41649104
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961-1619G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649104 | ||||||
chr22:41649126
|
C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0188a0001c0001t0001g0191others(4): Show | 7 | HG02293.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-1583dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649126 | |||||
chr22:41649135
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.961-1587_961-1586i others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649135 | |||||
chr22:41649137
|
A | AAT | 6 | a0001c0001t0001g0017a0001c0001t0001g0131a0001c0001t0001g0181others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-1585_961-1584i others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649137 | |||||
chr22:41649137
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0086 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.961-1585_961-1584i others(22): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649137 | |||||
chr22:41649137
|
A | AATATATA others(25): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.961-1585_961-1584i others(34): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649137 | |||||
chr22:41649137
|
A | AATATATA others(27): Show |
1 | a0001c0001t0001g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.961-1585_961-1584i others(36): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649137 | |||||
chr22:41649137
|
A | AATATATA others(35): Show |
1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.961-1585_961-1584i others(44): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649137 | |||||
chr22:41649137
|
A | AT | 9 | a0001c0001t0001g0005a0001c0001t0001g0123a0001c0001t0001g0125others(6): Show | 10 | HG00544.hp1 HG00673.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-1586_961-1585i others(3): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649137 | ||||||
chr22:41649137
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.961-1586_961-1585i others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649137 | ||||||
chr22:41649137
|
A | T | 12 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0001g0160others(9): Show | 12 | HG00642.hp1 HG00735.hp1 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.961-1586A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649137 | ||||||
chr22:41649138
|
AAAT | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-1583_961-1581d others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649138 | |||||
chr22:41649139
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(46): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(19): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(16): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0031 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(21): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(29): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(39): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0279 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(16): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0001g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(42): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(8): Show |
1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(21): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(16): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0037 | 3 | HG00673.hp2 NA18994.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.961-1583_961-1582i others(25): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(18): Show |
1 | a0001c0001t0001g0033 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(27): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(30): Show |
1 | a0001c0001t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(39): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAAAT others(32): Show |
1 | a0001c0001t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(41): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0038 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(20): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(13): Show |
2 | a0001c0001t0001g0294a0001c0001t0003g0003 | 3 | HG01934.hp1 HG02004.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.961-1583_961-1582i others(22): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(19): Show |
1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(28): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(23): Show |
1 | a0001c0001t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAAATA others(27): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0058 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.961-1583_961-1582i others(36): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAAATAT others(26): Show |
1 | a0001c0001t0001g0046 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(35): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(3): Show |
8 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0309others(5): Show | 8 | HG02109.hp2 HG02602.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-1583_961-1582i others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(16): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0003g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(22): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(23): Show |
5 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0083others(2): Show | 5 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-1583_961-1582i others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(25): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0281 | 3 | HG03225.hp2 NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.961-1583_961-1582i others(34): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(27): Show |
1 | a0001c0001t0001g0087 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.961-1583_961-1582i others(36): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(35): Show |
1 | a0001c0001t0002g0077 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(44): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAATATA others(37): Show |
6 | a0001c0001t0002g0051a0001c0001t0002g0062a0001c0001t0002g0068others(3): Show | 6 | NA18969.hp1 NA18982.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-1583_961-1582i others(46): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAAT | 6 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0186others(3): Show | 7 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-1583_961-1582i others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0001g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AAATATAT others(24): Show |
1 | a0001c0001t0001g0066 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.961-1583_961-1582i others(33): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0127 | 2 | HG01261.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.961-1569_961-1560d others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(17): Show |
1 | a0001c0001t0001g0085 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.961-1583_961-1560d others(26): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0091 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.961-1560_961-1559i others(28): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(21): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0084 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.961-1560_961-1559i others(30): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(23): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0093 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.961-1560_961-1559i others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AATATATA others(25): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0088 | 3 | HG00738.hp2 HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.961-1560_961-1559i others(34): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649139 | |||||
chr22:41649139
|
A | AT | 24 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0108others(21): Show | 24 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.961-1584_961-1583i others(3): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649139 | ||||||
chr22:41649139
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.961-1584_961-1583i others(35): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649139 | ||||||
chr22:41649139
|
A | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.961-1584A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649139 | ||||||
chr22:41649141
|
T | A | 21 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0075others(18): Show | 21 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.961-1582T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649141 | ||||||
chr22:41649143
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0297 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.961-1580T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649143 | ||||||
chr22:41649145
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0297 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.961-1578T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649145 | ||||||
chr22:41649156
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.961-1567A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649156 | ||||||
chr22:41649160
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0002g0067 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.961-1560_961-1559i others(40): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | ATATATAT others(17): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-1560_961-1559i others(26): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.961-1560_961-1559i others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0276 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.961-1560_961-1559i others(22): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | ATG | 8 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(5): Show | 9 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-1562_961-1561i others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | ATGTATG | 3 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280 | 3 | HG02976.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.961-1562_961-1561i others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649160 | |||||
chr22:41649160
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(38): Show | 45 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.961-1563A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649160 | ||||||
chr22:41649170
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG01070.hp1 HG01167.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.961-1553A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649170 | ||||||
chr22:41649190
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.961-1533A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649190 | ||||||
chr22:41649323
|
C | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.961-1400C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649323 | ||||||
chr22:41649324
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.961-1399G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649324 | ||||||
chr22:41649354
|
T | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.961-1369T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649354 | ||||||
chr22:41649376
|
A | T | 1 | a0001c0002t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.961-1347A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649376 | ||||||
chr22:41649592
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-1131C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649592 | ||||||
chr22:41649724
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.961-999G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649724 | ||||||
chr22:41649780
|
C | T | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(14): Show | 18 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.961-943C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649780 | ||||||
chr22:41649781
|
G | C | 1 | a0001c0001t0001g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.961-942G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649781 | ||||||
chr22:41649838
|
CA | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-874delA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41649838 | |||||
chr22:41649847
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-876A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649847 | ||||||
chr22:41649849
|
AT | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.961-873delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649849 | ||||||
chr22:41649850
|
T | A | 11 | a0001c0001t0001g0055a0001c0001t0001g0185a0001c0001t0001g0214others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-873T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649850 | ||||||
chr22:41649853
|
T | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0244others(2): Show | 5 | HG01175.hp1 HG02056.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.961-870T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649853 | ||||||
chr22:41649856
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.961-867T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649856 | ||||||
chr22:41649874
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.961-849G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649874 | ||||||
chr22:41649983
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-740G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649983 | ||||||
chr22:41649992
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-731C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649992 | ||||||
chr22:41650097
|
A | AT | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(20): Show | 24 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-615dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 41650097 | |||||
chr22:41650118
|
T | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.961-605T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41650118 | ||||||
chr22:41650285
|
T | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.961-438T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41650285 | ||||||
chr22:41650707
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.961-16C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41650707 | ||||||
chr22:41650943
|
G | A | 3 | a0001c0002t0001g0119a0001c0002t0001g0196a0001c0002t0001g0200 | 3 | NA19003.hp1 NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1129+52G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41650943 | ||||||
chr22:41651012
|
T | G | 1 | a0001c0001t0001g0287 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1129+121T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651012 | ||||||
chr22:41651063
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1129+172T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651063 | ||||||
chr22:41651068
|
G | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0259 | 2 | HG00621.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1129+177G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651068 | ||||||
chr22:41651352
|
GTTAAACA others(15): Show |
G | 1 | a0001c0001t0002g0067 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1129+464_1129+485d others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651352 | |||||
chr22:41651361
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0065 | 2 | HG02809.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1129+504_1129+516d others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1129+502_1129+516d others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129+501_1129+516d others(18): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0002g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1129+495_1129+516d others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
A | ATTTTTTT others(22): Show |
1 | a0001c0001t0002g0077 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1129+488_1129+516d others(31): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0002g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1129+487_1129+516d others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0093others(3): Show | 6 | HG00741.hp1 HG01167.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129+507_1129+516d others(12): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(4): Show |
A | 8 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0087others(5): Show | 8 | HG01099.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1129+506_1129+516d others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(5): Show |
A | 22 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0080others(19): Show | 22 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1129+505_1129+516d others(14): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(6): Show |
A | 68 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0028others(65): Show | 69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1129+504_1129+516d others(15): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(7): Show |
A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(92): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1129+503_1129+516d others(16): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0001g0066a0001c0002t0001g0138a0001c0002t0001g0145 | 3 | HG00099.hp2 HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1129+502_1129+516d others(17): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1129+501_1129+516d others(18): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0001g0191a0001c0001t0001g0272 | 2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1129+500_1129+516d others(19): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129+499_1129+516d others(20): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(13): Show |
A | 2 | a0001c0001t0001g0314a0001c0001t0002g0062 | 2 | HG03471.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1129+497_1129+516d others(22): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(14): Show |
A | 7 | a0001c0001t0001g0299a0001c0001t0001g0307a0001c0001t0001g0309others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129+496_1129+516d others(23): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(15): Show |
A | 10 | a0001c0001t0001g0009a0001c0001t0001g0298a0001c0001t0001g0300others(7): Show | 11 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1129+495_1129+516d others(24): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(16): Show |
A | 2 | a0001c0001t0001g0186a0001c0001t0001g0271 | 2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1129+494_1129+516d others(25): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(18): Show |
A | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(6): Show | 12 | HG01109.hp2 HG02071.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1129+492_1129+516d others(27): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(20): Show |
A | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1129+490_1129+516d others(29): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(21): Show |
A | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(14): Show | 18 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1129+489_1129+516d others(30): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(22): Show |
A | 6 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0182others(3): Show | 7 | NA18943.hp1 NA18951.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129+488_1129+516d others(31): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(23): Show |
A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1129+487_1129+516d others(32): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651361
|
ATTTTTTT others(24): Show |
A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1129+486_1129+516d others(33): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651361 | |||||
chr22:41651403
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1129+512T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651403 | ||||||
chr22:41651461
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 25 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129+570A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651461 | ||||||
chr22:41651521
|
A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1129+630A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651521 | ||||||
chr22:41651608
|
A | G | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.1129+717A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651608 | ||||||
chr22:41651644
|
C | T | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129+753C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651644 | ||||||
chr22:41651762
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1129+871G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651762 | ||||||
chr22:41651806
|
A | AT | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1129+922dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41651806 | |||||
chr22:41651852
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1129+961C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651852 | ||||||
chr22:41651863
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1129+972A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651863 | ||||||
chr22:41652035
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1129+1144C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652035 | ||||||
chr22:41652045
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1129+1154A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652045 | ||||||
chr22:41652069
|
C | T | 4 | a0001c0002t0001g0129a0001c0002t0001g0141a0001c0002t0001g0146others(1): Show | 4 | HG00438.hp2 NA18941.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129+1178C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652069 | ||||||
chr22:41652075
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1129+1184C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652075 | ||||||
chr22:41652190
|
G | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129+1299G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652190 | ||||||
chr22:41652241
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1130-1288A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652241 | ||||||
chr22:41652246
|
ATCT | A | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1130-1278_1130-127 others(7): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41652246 | |||||
chr22:41652346
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1130-1183A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652346 | ||||||
chr22:41652475
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-1054C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652475 | ||||||
chr22:41652495
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1130-1034A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652495 | ||||||
chr22:41652667
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1130-862A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652667 | ||||||
chr22:41652671
|
T | G | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130-858T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652671 | ||||||
chr22:41652698
|
C | CAG | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1130-830_1130-829d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 41652698 | |||||
chr22:41652860
|
GATGGGGT others(96): Show |
G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1130-668_1130-566d others(2): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652860 | ||||||
chr22:41652862
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1130-667T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41652862 | ||||||
chr22:41653155
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1130-374A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41653155 | ||||||
chr22:41653273
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1130-256G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41653273 | ||||||
chr22:41653886
|
G | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0184a0001c0001t0001g0186others(8): Show | 12 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1291+196G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41653886 | ||||||
chr22:41653888
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1291+198G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41653888 | ||||||
chr22:41653980
|
C | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 26 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.1291+290C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41653980 | ||||||
chr22:41654290
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+600A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41654290 | ||||||
chr22:41654311
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1291+621A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41654311 | ||||||
chr22:41654493
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+803G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41654493 | ||||||
chr22:41654770
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(21): Show | 28 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1291+1080C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41654770 | ||||||
chr22:41654824
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291+1134G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41654824 | ||||||
chr22:41655163
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1291+1473C>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655163 | ||||||
chr22:41655327
|
G | GT | 8 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0123others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-1561dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41655327 | |||||
chr22:41655327
|
GT | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00609.hp2 HG02451.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1292-1561delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41655327 | |||||
chr22:41655383
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1292-1520T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655383 | ||||||
chr22:41655518
|
A | G | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-1385A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655518 | ||||||
chr22:41655686
|
G | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-1217G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655686 | ||||||
chr22:41655698
|
C | CA | 11 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 12 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-1191dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41655698 | |||||
chr22:41655698
|
CAAAA | C | 15 | a0001c0002t0001g0119a0001c0002t0001g0129a0001c0002t0001g0137others(12): Show | 15 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.1292-1194_1292-119 others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41655698 | |||||
chr22:41655715
|
G | GT | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(102): Show | 110 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1292-1182dupT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41655715 | |||||
chr22:41655721
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1292-1182T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655721 | ||||||
chr22:41655787
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1292-1116C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655787 | ||||||
chr22:41655824
|
A | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | NA18961.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1292-1079A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655824 | ||||||
chr22:41655841
|
G | T | 21 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-1062G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655841 | ||||||
chr22:41655859
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1292-1044C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41655859 | ||||||
chr22:41656013
|
G | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0029others(38): Show | 42 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1292-890G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656013 | ||||||
chr22:41656112
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1292-791G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656112 | ||||||
chr22:41656201
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1292-702G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656201 | ||||||
chr22:41656215
|
C | CA | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0175others(12): Show | 15 | HG00558.hp2 HG01175.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1292-671dupA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41656215 | |||||
chr22:41656215
|
C | CAA | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1292-672_1292-671d others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41656215 | |||||
chr22:41656215
|
CA | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0298others(10): Show | 14 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-671delA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41656215 | |||||
chr22:41656247
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-656G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656247 | ||||||
chr22:41656359
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1292-544G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656359 | ||||||
chr22:41656528
|
A | AG | 5 | a0001c0001t0001g0272a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-375_1292-374i others(3): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656528 | ||||||
chr22:41656577
|
C | CAG | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(51): Show | 59 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-325_1292-324i others(4): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 41656577 | |||||
chr22:41656595
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1292-308C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656595 | ||||||
chr22:41656791
|
A | C | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-112A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 9/12 | chr22 | 41656791 | ||||||
chr22:41657188
|
G | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.1421+156G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657188 | ||||||
chr22:41657484
|
T | A | 1 | a0001c0001t0001g0281 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1421+452T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657484 | ||||||
chr22:41657490
|
T | TTTA | 23 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0034others(20): Show | 23 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1421+503_1421+505d others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
T | TTTATTA | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(20): Show | 23 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1421+500_1421+505d others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
T | TTTATTAT others(2): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0079others(1): Show | 4 | HG00621.hp2 HG01175.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421+497_1421+505d others(11): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
TTTA | T | 18 | a0001c0001t0001g0061a0001c0001t0001g0109a0001c0001t0001g0155others(15): Show | 18 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1421+503_1421+505d others(5): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
TTTATTA | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(35): Show | 40 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1421+500_1421+505d others(8): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
TTTATTAT others(2): Show |
T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1421+497_1421+505d others(11): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
TTTATTAT others(5): Show |
T | 6 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0039others(3): Show | 6 | HG01109.hp1 HG01261.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1421+494_1421+505d others(14): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657490
|
TTTATTAT others(14): Show |
T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1421+485_1421+505d others(23): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 41657490 | |||||
chr22:41657505
|
A | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0247a0001c0001t0001g0253 | 3 | HG02148.hp1 NA18953.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1421+473A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657505 | ||||||
chr22:41657600
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1421+568C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657600 | ||||||
chr22:41657758
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1422-494C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657758 | ||||||
chr22:41657861
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0191a0001c0001t0001g0195 | 3 | HG03225.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1422-391C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41657861 | ||||||
chr22:41658073
|
C | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 26 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.1422-179C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41658073 | ||||||
chr22:41658157
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0184a0001c0001t0001g0186others(8): Show | 12 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1422-95C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 10/12 | chr22 | 41658157 | ||||||
chr22:41658799
|
C | T | 17 | a0001c0001t0001g0206a0001c0001t0001g0222a0001c0001t0001g0233others(14): Show | 17 | HG00099.hp1 HG01081.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1522+447C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41658799 | ||||||
chr22:41658804
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1522+452G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41658804 | ||||||
chr22:41658873
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(1): Show | 4 | HG00673.hp2 NA18994.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1522+521A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41658873 | ||||||
chr22:41658957
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1522+605A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41658957 | ||||||
chr22:41659190
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0038 | 3 | HG00408.hp2 HG00423.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1522+838T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659190 | ||||||
chr22:41659456
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1522+1104T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659456 | ||||||
chr22:41659502
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1522+1150G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659502 | ||||||
chr22:41659712
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1522+1360C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659712 | ||||||
chr22:41659718
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(4): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1522+1366C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659718 | ||||||
chr22:41659963
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1523-1368G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659963 | ||||||
chr22:41659993
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1523-1338A>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41659993 | ||||||
chr22:41660159
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1523-1172G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660159 | ||||||
chr22:41660230
|
A | C | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1523-1101A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660230 | ||||||
chr22:41660263
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1523-1068A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660263 | ||||||
chr22:41660300
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0290 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1523-1031T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660300 | ||||||
chr22:41660727
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1523-604C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660727 | ||||||
chr22:41660952
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1523-379T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660952 | ||||||
chr22:41660988
|
C | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 25 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1523-343C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660988 | ||||||
chr22:41660989
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1523-342G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41660989 | ||||||
chr22:41661044
|
TA | T | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1523-274delA | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 41661044 | |||||
chr22:41661096
|
G | T | 9 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0062others(6): Show | 9 | HG02071.hp2 NA18969.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1523-235G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41661096 | ||||||
chr22:41661199
|
G | T | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1523-132G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41661199 | ||||||
chr22:41661290
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024 | 4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523-41C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41661290 | ||||||
chr22:41661291
|
G | C | 1 | a0001c0002t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1523-40G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 11/12 | chr22 | 41661291 | ||||||
chr22:41661593
|
G | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1636+149G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41661593 | ||||||
chr22:41661723
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1636+279T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41661723 | ||||||
chr22:41661859
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636+415C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41661859 | ||||||
chr22:41661904
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG01433.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1636+460G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41661904 | ||||||
chr22:41662027
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1636+583G>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662027 | ||||||
chr22:41662332
|
TATATATA others(4): Show |
T | 5 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0189others(2): Show | 6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636+889_1636+899d others(13): Show |
XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662332 | ||||||
chr22:41662344
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1636+900G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662344 | ||||||
chr22:41662489
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1636+1045T>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662489 | ||||||
chr22:41662588
|
T | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 17 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1637-1034T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662588 | ||||||
chr22:41662777
|
T | C | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637-845T>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662777 | ||||||
chr22:41662842
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1637-780G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662842 | ||||||
chr22:41662945
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1637-677G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662945 | ||||||
chr22:41663005
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1637-617C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41663005 | ||||||
chr22:41663056
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637-566C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41663056 | ||||||
chr22:41663101
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 6 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637-521A>C | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41663101 | ||||||
chr22:41663426
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1637-196G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41663426 |