Item | Value |
---|---|
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 | MSGWE others(604): Show |
chr22 | 41616295 | 41669041 |
a0002 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | MSGWE others(604): Show |
chr22 | 41616295 | 41669041 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1827 | 269 | 86 | 50 | 97 | 9 | 25 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGTC others(1822): Show |
chr22 | 41616295 | 41669041 | ||
a0001c0002 | 0/0 | 1827 | 54 | 2 | 12 | 24 | 5 | 11 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGTC others(1822): Show |
chr22 | 41616295 | 41669041 | ||
a0002c0003 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGTC others(1822): Show |
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 | ATGCG others(2117): Show |
chr22 | 41616295 | 41669041 |
a0001c0001t0002 | 0/0 | 2122 | 8 | 0 | 0 | 8 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGCG others(2117): Show |
chr22 | 41616295 | 41669041 |
a0001c0001t0003 | 0/0 | 2122 | 3 | 0 | 3 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGCG others(2117): Show |
chr22 | 41616295 | 41669041 |
a0001c0002t0001 | 0/0 | 2122 | 54 | 2 | 12 | 24 | 5 | 11 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGCG others(2117): Show |
chr22 | 41616295 | 41669041 |
a0002c0003t0002 | 0/0 | 2122 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | ATGCG others(2117): Show |
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 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | 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 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0021 | 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 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0036 | 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 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0062 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0069 | 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 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0178 | 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 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0202 | 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 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0115 | 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 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
a0002c0003t0002g0061 | 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 | g0158 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0167 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | GBR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0161 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | 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 | g0126 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | 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 | g0282 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0183 | 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 | g0172 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0052 | 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 | g0053 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | CLM | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0156 | EUR | IBS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0173 | 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 | g0092 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CDX | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0055 | 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 | g0254 | AMR | PEL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0166 | 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 | g0299 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0054 | 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 | g0114 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0135 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | STU | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19000 | hp2 | a0002 | c0003 | t0002 | g0061 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0223 | 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 | g0150 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0280 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0016 | 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 | g0097 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0102 | REF | REF | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0079 | REF | REF | XRCC6_chr22_41616295_41669041 | XRCC6 | chr22 | 41616295 | 41669041 |
view | 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 |
view | 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 |
view | 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 | a0001c0001t0002 a0002c0003t0002 |
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 |
view | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0028 a0001c0002t0001g0026 a0001c0002t0001g0027 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0002t0001g0284 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0282 | 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 | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0281 | 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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0002t0001g0279 a0001c0002t0001g0280 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | 6 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): 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 | a0001c0001t0001g0092 | 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 | a0001c0002t0001g0098 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0002t0001g0266 |
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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 |
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 | a0001c0001t0001g0100 | 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 | a0001c0002t0001g0101 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0287 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.82+2425C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 2/12 | chr22 | 41624511 | |||||||
chr22:41624719 | C | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
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 | a0001c0001t0001g0289 | 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 | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0289 others(14): 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | 6 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0300 others(3): 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0263 | 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 | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0289 others(14): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0261 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
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 | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | a0001c0001t0001g0105 a0001c0001t0001g0263 |
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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0014 a0001c0001t0001g0259 a0001c0001t0001g0260 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(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 | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(68): Show |
74 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(71): 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 | a0001c0001t0001g0013 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0263 | 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 | a0001c0002t0001g0108 a0001c0002t0001g0109 |
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 | a0001c0002t0001g0239 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0234 a0001c0002t0001g0233 others(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 | 1 | a0001c0001t0003g0002 | 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 | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0083 others(8): 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 | a0001c0001t0001g0290 | 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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(48): 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0002t0001g0238 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0002t0001g0122 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | 6 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0300 others(3): 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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0028 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0148 | 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 | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0289 others(14): 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 | a0001c0001t0001g0025 a0001c0001t0001g0103 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0194 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(45): 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0154 | 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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): 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 | 18 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(48): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0002t0001g0191 | 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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | a0001c0001t0001g0100 | 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0033 |
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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | a0001c0001t0001g0290 | 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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(48): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0190 a0001c0002t0001g0111 a0001c0002t0001g0189 |
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 | a0001c0001t0001g0190 a0001c0002t0001g0189 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0001g0188 | 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 | a0001c0002t0001g0142 | 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 |
252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0141 | 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 | a0001c0002t0001g0157 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0044 | 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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0002t0001g0108 a0001c0002t0001g0109 |
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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0195 others(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 | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(198): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): 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 |
20 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 6 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0300 others(3): 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0219 others(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 | a0001c0002t0001g0115 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0158 | 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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0077 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0116 a0001c0001t0001g0124 others(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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0263 | 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 | a0001c0002t0001g0128 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0002t0001g0253 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(44): 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0289 others(14): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0140 | 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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0002t0001g0159 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(196): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): 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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0092 others(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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0220 | 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 | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | a0001c0001t0001g0226 | 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 | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(198): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.196-164C>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 3/12 | chr22 | 41635949 | |||||||
chr22:41636099 | A | AT | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0077 others(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 | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): 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 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0251 | 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 | a0001c0002t0001g0238 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0290 | 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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | 75 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0034 others(72): 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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0262 | 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 | a0001c0002t0001g0142 | 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0224 others(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 | 8 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0262 others(5): 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 | a0001c0001t0001g0015 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | 24 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(21): 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 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0088 others(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 | 60 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0023 others(57): Show |
64 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(61): 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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0034 others(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 | 36 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0025 others(33): 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 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(15): 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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0163 others(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 |
220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0131 | 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 | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0082 | 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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(48): 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 | 6 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0300 others(3): 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(198): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.773+3515delC | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641305 | |||||||
chr22:41641342 | G | A | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.773+3565C>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 6/12 | chr22 | 41641356 | |||||||
chr22:41641608 | C | A | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0094 | 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 | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0155 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0262 | 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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(49): 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 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0043 |
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 | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(24): 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 | 19 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0220 others(16): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0100 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): 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 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(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 | a0001c0002t0001g0115 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0274 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0262 a0001c0001t0001g0285 others(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 | a0001c0002t0001g0284 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 |
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 | a0001c0001t0001g0031 | 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 | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(115): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): 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 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0103 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0263 |
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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(42): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0127 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0092 others(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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0002g0071 | 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 | a0001c0002t0001g0142 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.961-1722G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649001 | |||||||
chr22:41649005 | A | AAAC | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0166 a0001c0001t0001g0259 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0223 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0145 a0001c0001t0001g0188 others(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 |
1 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0285 a0001c0001t0003g0002 |
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 | a0001c0001t0001g0008 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0052 | 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 |
7 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0072 others(4): 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0003g0002 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0272 |
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 | a0001c0001t0002g0080 | 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 | a0001c0001t0002g0057 a0001c0001t0002g0066 a0001c0001t0002g0073 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0069 | 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 | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(110): Show |
118 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(115): 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 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0288 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0288 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0002g0071 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | 39 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(36): 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 | 4 | a0001c0001t0001g0009 a0001c0001t0001g0064 a0001c0001t0001g0094 others(1): 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 | a0001c0001t0001g0033 | 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 | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
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 | a0001c0002t0001g0122 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0232 | 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 | 16 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 193 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(190): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.961-873delT | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41649849 | |||||||
chr22:41649850 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0120 others(7): 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 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0058 | 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 | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.961-605T>G | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 7/12 | chr22 | 41650118 | |||||||
chr22:41650285 | T | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): 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 | a0001c0002t0001g0159 | 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 | a0001c0002t0001g0121 a0001c0002t0001g0233 a0001c0002t0001g0237 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0244 |
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 | a0001c0001t0002g0071 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0002g0057 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0087 others(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 | 21 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0055 others(18): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(90): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): 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 | a0001c0001t0001g0070 a0001c0002t0001g0159 a0001c0002t0001g0167 |
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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0263 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0016 a0001c0001t0002g0066 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0289 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0042 | 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 | 16 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): 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 | a0001c0001t0001g0011 a0001c0001t0001g0100 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): 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 | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1129+630A>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 8/12 | chr22 | 41651521 | |||||||
chr22:41651608 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): 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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0019 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0294 | 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 | a0001c0002t0001g0143 a0001c0002t0001g0164 a0001c0002t0001g0168 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0262 | 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 | 184 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(181): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0257 | 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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0001g0263 | 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 | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0219 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0288 | 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 | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(20): 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0002t0001g0157 | 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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0121 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0104 | 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 | a0001c0002t0001g0108 a0001c0002t0001g0109 |
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 | 20 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0124 others(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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(168): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(49): 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 | a0001c0001t0001g0262 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): 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 | a0001c0001t0001g0272 | 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 | 22 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(19): 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 | 22 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): 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 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0023 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): 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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0180 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0232 |
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 | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): 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 | a0001c0001t0001g0012 a0001c0001t0001g0219 a0001c0001t0001g0221 others(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 | 16 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0174 others(13): Show |
16 | HG00099.hp1 HG01081.hp2 HG01258.hp2 others(13): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0043 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): 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 | a0001c0001t0001g0263 | 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0220 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): 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 | a0001c0001t0001g0177 | 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 | 21 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): 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 | a0001c0001t0002g0057 a0001c0001t0002g0059 a0001c0001t0002g0066 others(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 | 5 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 |
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 | a0001c0002t0001g0157 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0129 | 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 | 15 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(204): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1637-780G>A | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41662842 | |||||||
chr22:41662945 | G | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(204): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0262 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1637-196G>T | XRCC6 | ENSG00000196419.13 | transcript | ENST00000360079.8 | protein_coding | 12/12 | chr22 | 41663426 |